PROCESS FOR MODIFYING THE ARCHITECTURE AND IMPROVING THE YIELD OF CROP PLANTS

This invention lies within the technical field of agriculture. The various aspects of the invention can also be applied to the crop productivity for food and feed production as well as biomass production for the energy sector, specifically the development of transgenic plants for use in obtaining biofuels, such as in the production of bioethanol.

STATE OF THE ART

Plant architecture has a marked effect on the yield of plants. This influence is exerted through photosynthetic potential, the transfer of assimilated materials and nutrients to the different organs of the plant, and finally manifests itself in the potential growth and yield of the plant.

Cell differentiation is a fundamental process in all organisms and, together with cell proliferation, dictates the size and shape of the organisms (Ramirez-Parra et al . , Int. J. Dev. Biol. 2005). Thus, modification of plant architecture and yield depend at the most fundamental level on regulating cell proliferation and differentiation. The molecular mechanisms controlling the cell cycle in plants are well known (De Veylder et al., Nat. Rev. Mo. Cell Biol. 2007) and are largely conserved relative to the mechanisms that control this cycle in other eukaryotes. Many of the methods for modifying the architecture of plants are based on controlling cell proliferation, for example by altering the dormancy/activation of buds {TCP genes) or altering the balance of proliferation in meristems or organ primordia (STM, WUS, AS1, SWP genes) .

On the other hand, the mechanisms responsible for initiating cell differentiation are very poorly understood. In addition, it is not known which genetic factors initiate cell differentiation. In animals, it is assumed that the start of differentiation involves a transcriptional re-ordering which makes it possible to activate developmental programmes which are silenced in progenitor stem cells. There is evidence that silencing of these programmes is due to blocking the productive transcriptional elongation of developmental regulatory genes (Guenther et al . , Cell 2007; Stock et al . , Nature Cell Biol. 2007), but the factors which activate this elongation upon differentiation have not been identified.

An example of manipulating plant architecture and crop yield is disclosed in US 2009/0320163 which describes a method for obtaining transgenic plants whose plant architecture has been modified through alterations in the expression of PDR genes (Plant Developmental Regulators). These genes have similarities with phosphatidyl ethanolamide binding proteins (PEBPs), which act as inhibitors in the signalling cascades of MAP kinases, with the result that transgenic plants with a greater number of seeds, a better plant foliage architecture, stronger stems and a larger plant biomass in general are obtained .

Another specific example is transgenic Arabidopsis plants which have reduced levels of expression of AtMago mRNA (RNAi- AtMago plants) . It is known that the Mago Nashi gene is involved in organisation of apical and root meristems, but not floral meristems, and also affects the formation of pollen and the development of seeds in Arabidopsis (Nam-Il et al. Plant Science 176 (2009) 461-469) . RNAi-AtMago plants generally presented delayed vegetative growth, producing a larger number of leaves of smaller size, apical meristems with excessively vacuolated cells and large intercellular spaces giving rise to shorter and branched stems, smaller root meristems and shorter lateral roots with premature differentiation of root hairs. RNAi-AtMago plants also show reduced pollen production and germination, occasionally giving rise to non-viable seeds.

At the present time, there are many methods available for modifying root and above-ground architecture and improving crop yields, including modifying the size of meristems. These methods are based on changing the expression of genes that have specific effects in each meristem, for example in shoot apical meristems through altering the expression of genes such as STM, CLV3 or WUS, in root apical meristems through altering the expression of genes such as PLT, SHY2 or RGFl, and in general modifying the synthesis, transport and signalling of auxins and cytokinins.

Nevertheless, to the best of our knowledge, in the state of the art, no gene has been identified which acts directly to switch on cell differentiation. The decision as to whether to differentiate or not is shared by cells of all the meristems throughout the plant as well as in the developing embryo, which means that identification of a conserved genetic switch controlling this fate decision makes it possible to control cell differentiation throughout the plant in a targeted way. This includes, for example, control during embryogenesis and in the apical, floral and vascular meristems. Modulation of this unique switch is thus a novel mechanism, directly applicable to all the meristems of the plant and in embryos, which makes it possible to activate, block or delay the initiation of differentiation in a highly specific way.

The present invention identifies this common switch which initiates cell differentiation. The invention is aimed at methods for generating transgenic plants with altered cell differentiation and at transgenic plants obtained through such methods. Plants with altered cell differentiation are desirable tools in agriculture as they can be used to increase yield and the present invention is aimed at addressing the need for more productive crop plants.

BRIEF DESCRIPTION OF THE INVENTION The invention relates to methods for improving the root and above-ground architecture of plants to obtain better crop yields. According to the invention, the MINIYO and RTRl genes are good tools for genetic manipulation to control the timing of the onset of differentiation in embryogenesis and in all of the meristems of the plant. According to the invention, MINIYO and RTRl nucleic acid sequences can therefore be used to regulate the size and number of plant embryos, meristems and the organs generated from them. MINIYO and RTRl interact and regulate the activity of RNA polymerase II (Pol II), and are jointly involved in the activation of transcriptional elongation and the expression of growth programmes which control the initiation of cell differentiation in the plant. The transgenic plants according to the invention differ from the parent plants in that they have an increase or decrease in the expression and/or genetic activity of MINIYO and/or RTRl, including the Arabidopsis thaliana AtMINIYO and AtRTRl genes or their orthologues in other plant species. This gives rise to advance, delay or blocking of the initiation of differentiation in apical, floral and/or root meristems, thereby modifying the number and size of meristems and/or the number and size of the organs generated from them. Preferably, the transgenic plants according to the invention have partly or wholly reduced expression of the MINIYO and/or RTRl genes, including AtMINIYO and AtRTRl or their orthologues in other plant species, in such a way that there is an improvement in their plant architecture which leads to improved crop yields in comparison with the wild plants. For example, the transgenic plants have meristems with increased size (greater stem thickness), and they also have ectopic meristems giving rise to additional inflorescences, multiple flowers and/or a large number of side roots and seeds with double embryos.

In a first aspect, the invention relates to an isolated nucleic acid sequence comprising a nucleotide sequence encoding for an amino acid sequence of SEQ ID NO: 5 or an orthologue thereof. In a second aspect, the invention relates to an isolated nucleic acid sequence comprising a nucleotide sequence encoding for amino acid sequence of SEQ ID NO: 11 or an orthologue thereof.

In a further aspect, the invention relates to an expression vector comprising one or more of the isolated nucleic acid sequence (s) of the invention. In another aspect, the invention relates to a transgenic plant wherein the activity of a MINIYO and/or RTR1 polypeptide is inactivated, repressed or down-regulated.

In an additional aspect, the invention relates to a transgenic plant wherein the activity of a MINIYO and/or RTR1 polypeptide is increased or up-regulated.

In a further aspect, the invention relates to a use of a MINIYO and/or RTR1 polypeptide to control the initiation of cell differentiation in plant apical, root and/or floral meristems .

In an additional aspect, the invention relates to a use of a MINIYO and/or RTR1 polypeptide to delay the initiation of cell differentiation in plant apical, root and floral meristems.

In another aspect, the invention relates to a method for delaying the onset of cell differentiation and increasing the number of undifferentiated cells in a plant said method comprising decreasing the activity of a MINIYO and/or RTR1 polypeptide .

In another aspect, the invention relates to a method for increasing cell differentiation in a plant said method comprising increasing the activity of a MINIYO and/or RTR1 polypeptide . In further aspect, the invention relates to an isolated nucleic acid sequence comprising SEQ ID No. 48 or SEQ ID No. 49 and uses thereof to direct spatial and temporal expression of target genes.

Also included are methods of producing transgenic plants with altered activity of a MINIYO and/or RTRl polypeptide and method of increasing yield by decreasing the activity of activity of a MINIYO and/or RTRl polypeptide.

DETAILED DESCRIPTION OF THE INVENTION

The present invention will now be further described. In the following passages, different aspects of the invention are defined in more detail. Each aspect so defined may be combined with any other aspect or aspects unless clearly indicated to the contrary. In particular, any feature indicated as being preferred or advantageous may be combined with any other feature or features indicated as being preferred or advantageous.

The practice of the present invention will employ, unless otherwise indicated, conventional techniques of botany, microbiology, tissue culture, molecular biology, chemistry, biochemistry and recombinant DNA technology, which are within the skill of the art. Such techniques are explained fully in the literature.

The basis of this invention is the characterisation of the AtMINIYO (At4g38440) and AtRTRl (At5g26760) genes which comprise a highly conserved, common molecular switch that initiates differentiation in all plants. The acronym IYO is used herein to refer to the AtMINIYO gene. We have identified and characterised the mutant miniyo-1 (iyo- 1) which shows a delay in the initiation of cell differentiation (Figures 1 and 2). Through positional mapping, we have shown that phenotypes with delayed differentiation in iyo-1 plants are due to a point mutation in the IYO gene (At4g38440, Figure 3A-B) . The iyo-1 allele causes a change in amino acid 962 from a glycine to a glutamate residue. This disrupts an RGG RNA-binding motif which is strictly conserved in all MINIYO orthologues (Figures 3B and 18a) . This mutation gives rise to a partial loss of activity in the IYO gene and results in delayed onset of differentiation in all the meristems of the plant (Figure 1) . As a consequence, ectopic stem cells are generated (Figures 1A-E, 2) and these give rise to new shoot and root meristems, new floral meristems (double and triple flowers), adjacent groups of stomas (Figure 1F-I) and a larger number of lateral roots, including in positions in which they do not develop in wild-type plants (Figure 2) . Total blocking of IYO activity causes embryogenesis to be arrested at early stages (Figure 3E-F) .

In addition, the combination of the hypomorphic iyo-1 allele with null alleles (iyo-2 or iyo-3) gives rise to the formation of seeds with double embryos (Figures 1J and 3D) which mature and upon germinating give rise to plants with multiple meristem poles which generate rudimentary leaves (Figure IK) . Also in the case of the iyo-1 allele there are cases of double embryos which develop in a similar way to wild-type embryos (Figure 1L) .

Expression of the IYO gene is regulated at the transcriptional and post-transcriptional level to direct its activity specifically to the periphery of the meristems where differentiation begins (Figures 4 and 5) . The promoter of the IYO gene is exclusively active in developing seeds, in meristems and in cells in the early stages of differentiation (Figures 4A-B, 5C-E) . Moreover, specific signal sequences present in the IYO protein restrict nuclear accumulation of the protein exclusively to cells which are about to begin differentiation (Figures 4B-F, 5G-I) . The protein is excluded from the nucleus in proliferating meristematic cells through active Exportinl-dependent export, as it is inhibited by treatment with leptomycin B (Figure 5j) . The overexpression of IYO or its fusions with proteins or peptides such as GFP, HA, FLAG under the control of the constitutive 35S promoter leads to premature differentiation in meristems, including in the rib meristem with the consequent shortening of internodes and the compaction of inflorescences (Figure 6B-C) , and even to meristem consumption (Figure 7 ) .

The IYO gene codes for a protein which interacts physically with RNA polymerase II (Pol II) and with elongation complexes (Figure 8A-B, G-I) and which activates transcriptional elongation (Figure 8C, E-F) and the expression of development programmes directing differentiation (Figures 8C-D, 6A) . Through the analysis of co-expressed genes, we identified the gene At5g26760 (AtRTRl) which has a Pearson correlation coefficient of r = 0.625 with IYO. At5g26760 codes for a protein which is highly conserved in all plant species, is homologous to the RTR1 protein from Saccharomyces cerevisae, and also has homologues in animals. RTR1 interacts with Pol II and results have recently been published which indicate that it acts as a transition phosphatase for Pol II in yeast (Mosley et al . , 2009) . This phosphatase is thought to be involved in the dephosphorylation of serine 5 in the C- terminal domain of the RPB1 (CTD) sub-unit, a modification preceding phosphorylation in serine 2 which is necessary for Pol II to enter into productive elongation. Bearing in mind the homology between At5g26760 and this phosphatase which acts in the transition between initiation and elongation in transcription and its co-expression with the IYO gene, which is an activator of transcriptional elongation, we postulate that At5q26160 /AtRTRl is jointly involved with the IYO gene in the activation of transcriptional elongation and the initiation of cell differentiation in plants.

As a first step in analysing the function of AtRTRl, we studied two mutant alleles in the SALK collection. The allele atrtrl-1 ( SALK_012339 ) has an insertion of T-DNA in the first exon which gives rise to the total loss of function of RTRl . Homozygous atrtrl-1 plants arrest their growth during early stages of embryogenesis (Figure 9) . The arrested embryos have a phenotype which is very similar to strong alleles of iyo, comprising an almost total block on cell differentiation and the production of twin embryos from suspensor cells. The atrtrl-2 allele ( SALK_115762 ) has a T-DNA insertion in the third intron of the gene, which is spliced out but with low efficiency, resulting in very low accumulation of the full- length transcript. The atrtrl-2 allele results in a partial loss of AtRTRl activity and phenocopies almost exactly the weak allele iyo-1. atrtrl-2 plants have delayed onset of differentiation in the different meristems of the plant and therefore maintain ectopic stem cells that generate additional shoot, flower and root meristems (Figure lOA-C) and ectopic meristemoids (Figure 11) . Ectopic embryos that germinate and give rise to cloned plants are also generated.

The phenotype of a double iyo-latrtrl-2 mutant shows a clear interaction between the IYO and AtRTRl genes in control of the initiation of cell differentiation. These double mutants have a total block on differentiation that gives rise to growth in the form of a mass of undifferentiated cells (Figure 10D) . In addition, we have demonstrated that the over-expression of IYO in a mutant atrtrl-2 ecotype does not give rise to any phenotype, demonstrating that the RTRl gene is necessary for the function of MINIYO.

In order to study the expression of RTRl, we generated transgenic plants expressing the promoter of RTRl and the first three exons and introns of RTRl translationally fused to the UidA (GUS) reporter gene. This construct directs the activity of GUS specifically to meristems and differentiating tissues (Figure 10E) , in a pattern which is very similar to that of plants which express GUS under the promoter of IYO, which is consistent with the high level of co-expression of the corresponding transcripts and is compatible with the fact that both genes function together and in a coordinated way. Furthermore, we analysed the pattern of accumulation of AtRTRl fused to the GFP reporter under the control of the constitutive CaMV 35S promoter . In the same way as IYO-GFP, the fusion product AtRTRl-GFP does not accumulate in the nuclei of undifferentiated cells (Figure 10F) , being excluded through active export dependent on Exportinl (Figures 10F and 12) .

Although the bulk of AtRTRl is present in the cytosol, we found high levels of nuclear fluorescence reconstitution when split YFP fused to IYO and AtRTRl was expressed in Nicotiana benthamiana leaves (Figures 12-14) . This confirms that IYO and AtRTRl interact physically, and that they do so in the nucleus. Moreover, reconstituted YFP stabilizes complexes, and this leads to large accumulation of AtRTRl in the nucleus, which suggest that complex formation serves to retain AtRTRl in that compartment. To test this, we analyzed the subcellular distribution of AtRTRl in the presence or absence of co- expressed IYO. These experiments confirmed that co-expressed IYO increases the accumulation of AtRTRl in the nucleus.

These results demonstrate that MINIYO and RTR1 form a complex in the nucleus and that they have a common and shared function in combining to initiate cell differentiation by the activation of transcriptional elongation through the interaction and modification of Pol II.

We have shown that downregulation of MINIYO and/or RTRl genes or their proteins leads to a delayed onset of differentiation, increased meristem size/number and ectopic meristems. Thus, downregulation of MINIYO and/or RTRl can be useful in increasing plant yield. The term "yield" as described herein relates to yield-related traits. Specifically, these include an increase in biomass and/or seed yield. This can be achieved by increased growth. An increase in yield can be, for example, assessed by the harvest index, i.e. the ratio of seed yield to aboveground dry weight. Thus, according to the invention, yield comprises one or more of: increased seed yield per plant, increased seed filling rate, increased number of filled seeds, increased harvest index, increased number of seed capsules/pods, increased seed size, increased growth or increased branching, for example inflorescences with more branches. Preferably, yield comprises an increased number of seed capsules/pods and/or increased branching. Yield is increased relative to control plants. An increase in yield may be about 5, 10, 20, 30, 40, 50% or more compared to a control plant .

In contrast, overexpression of MINIYO and/or RTRl genes can be used to eliminate branches of the inflorescence meristem in crops where this is useful. The invention is therefore based on the generation of plants having either increased or reduced activity of MINIYO and/or RTRl genes or their proteins, including AtMINIYO and AtRTRl or their orthologues in other plant species, to advance or delay the onset of differentiation in the meristems, at the required time in each case. Thus, the activity of MINIYO and/or RTRl, including AtMINIYO and AtRTRl or their orthologues in other plant species, may be inactivated, repressed or downregulated . In another aspect, the activity of MINIYO and/or RTRl, including AtMINIYO and AtRTRl or their orthologues in other plant species, is increased or up-regulated. Transgenic or mutant plants which express MINIYO and/or RTRl genes, including AtMINIYO and AtRTRl or their orthologues in other plant species, but where the function of the protein is partly lost, may be obtained according to the various aspects of the invention.

Alternatively, null mutants are obtained which are transformed with or carry attenuated or mutant versions of MINIYO or RTRl genes, such as the iyo-1 alleles and atrtrl-2 alleles or a combination thereof, or other alleles which have mutated amino acids in regions which are highly conserved in MINIYO and RTRl proteins, including AtMINIYO and AtRTRl or their orthologues in other plant species (Figures 18 and 21) . The expected phenotypes are similar to those already observed in Arabidopsis, i.e.: larger meristems and directly generated organs (thicker stems), ectopic meristems which give rise to additional inflorescences, duplicated flowers, a larger number of side roots and seeds with double embryos.

Throughout this disclosure, MINIYO and RTRl are used to refer to the genes homologous/proteins to the Arabidopsis AtMINIYO and AtRTRl genes/proteins respectively, as described herein.

Specifically, a skilled person would therefore understand that the invention not only relates to isolated AtMINIYO and AtRTRl genes/proteins as defined in SEQ ID No. 1, 8, 5 and 11 and their uses in the various aspects of the invention, but that the present invention relates to methods and uses of homologues and orthologues of the AtMINIYO or AtRTRl genes and their polypeptides in other plant species, including transgenic plants where expressing or activity of such an orthologous gene/protein is increased or decreased.

Thus, in a first aspect, the invention relates to an isolated nucleic acid molecule or sequence comprising a nucleic acid molecule of SEQ ID No. 1 coding for the AtMINIYO protein of SEQ ID No. 5, or its orthologue in another plant species. In another aspect, the invention relates to an isolated nucleic acid sequence or molecule comprising a nucleic acid of SEQ ID No. 8 coding for the AtRTRl protein of SEQ ID No. 11 or its orthologue in another plant species. As explained herein, said nucleic acid molecule (s) control (s) the initiation of cell differentiation in apical, root and floral meristems of the plant. Preferably, the nucleic acid molecule (s) is/are homologous to the corresponding nucleic acid molecules which code for the AtMINIYO proteins of SEQ ID No . 5 or its orthologue in another plant species, and/or the AtRTRl protein of SEQ ID No. 11 or its orthologue in another plant species. In a preferred embodiment of the invention, the nucleic acid molecule is characterised by interacting and/or modifying the RNA polymerase II (Pol II) involved in the activation of transcriptional elongation and the expression of developmental programmes which direct the initiation of cell differentiation in seeds and in all the apical, root and floral and other meristems of the plant. In a preferred embodiment, the protein AtMINIYO or its orthologue in other plant species, and the protein AtRTRl or its orthologue in other plant species, interact and/or modify the RNA polymerase II (Pol II), and are jointly involved in the activation of transcriptional elongation and the expression of developmental programmes which direct the initiation of cell differentiation in seeds and in all the apical, root and floral and other meristems of the plant.

This invention also protects an isolated nucleic acid comprising a nucleotide sequence coding for an amino acid sequence of the protein IYO and/or the protein AtRTRl, or their orthologues in another plant species, which are at least 30% identical to the sequences coded by SEQ ID NO: 1 and/or SEQ ID NO: 8 to control the initiation of cell differentiation in seeds and in apical, root and floral and other meristems of a plant, and their uses, preferably their use to control the initiation of cell differentiation in seeds and in apical, root and floral meristems of a plant.

Accordingly, the invention relates to an isolated nucleic acid sequence comprising or consisting of SEQ No. 1 or 8 or a homologue, orthologue or functional variant thereof. In one embodiment, the isolated nucleic acid sequence comprises or consists of SEQ No. 1 or 8. In another embodiment, the isolated nucleic acid sequence comprises or consists of a nucleic acid sequence that encodes for an orthologue of the protein identified in SEQ No. 5 or 11.

As used herein, the words "nucleic acid", "nucleic acid sequence", "nucleic acid molecule", "nucleotide", or "polynucleotide" are intended to include DNA molecules (e.g., cDNA- as is the case for SEQ ID NO: 1 and SEQ ID NO: 8- or genomic DNA), RNA molecules (e.g., mRNA) , natural occurring, mutated, synthetic DNA or RNA molecules, and analogs of the DNA or RNA generated using nucleotide analogs. The skilled person will understand that where the nucleic acid according to the invention includes RNA, reference to the sequence shown should be construed as reference to the RNA equivalent, with U substituted for T. It can be single-stranded or double- stranded. Such nucleic acids or polynucleotides include, but are not limited to, coding sequences of structural genes, anti-sense sequences, and non-coding regulatory sequences that do not encode mRNAs or protein products. These terms also encompass a gene. The term "gene" or "gene sequence" is used broadly to refer to a DNA nucleic acid associated with a biological function. Thus, genes may include introns and exons as in the genomic sequence, or may comprise only a coding sequence as in cDNAs, and/or may include cDNAs in combination with regulatory sequences. The sequences may also be synthetically made sequences. The nucleic acid may be wholly or partially synthetic, depending on design.

The term "functional part or functional variant" as used herein refers to a variant gene or polypeptide sequence or part of the gene or polypeptide sequence which retains the biological function of the full non-variant sequence, i.e. acts as a molecular switch to initiate cell differentiation. Variant degenerate sequences of the nucleotide sequences according to the invention whose product is a protein having the same function as the protein coded by each of the sequences SEQ ID NO: 5 and SEQ ID NO: 11 are thus included within the scope of the invention. The amino acid sequence may be coded by any nucleotide sequence which gives rise to any of the amino acid sequences according to the invention. Due to the fact that the genetic code is degenerate, the same amino acid may be coded for by different codons (triplets), and thus the same amino acid sequence may be coded for by different nucleotide sequences. The homologue, orthologue or functional variant of SEQ ID No.

1 or 8 encodes a polypeptide that is 30%-99% identical to a sequence encoded by SEQ No . 1 or 8 For example, the polypeptide of the invention has , in increasing order of preference , at least 30%, 31%, 32 "o , 33 "o , 34%, 35"o , 36%, 37%,

38%, 39%, 40%, 41%, 42%, 43%, 44%, 45%, 46%, 47%, 48%, 49%,

50%, 51%, 52 'o _f 53 'o _f 54%, 55'o ψ 56%, 57%, 58%, 59%, 60%, 61%,

62%, 63%, 64%, 65%, 66%, 67%, 68%, 69%, 70%, 71%, 72%, 73%,

74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%,

86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%,

98%, or 99% overall sequence identity to the amino acid represented by SEQ ID NO: 5 or 11, respectively, and/or represented by the AtMINIYO or AtRTRl orthologues and paralogues shown herein.

In one embodiment, the isolated nucleic acid of the invention encodes a polypeptide that is at least 30% identical to a sequence encoded by SEQ No. 5 or 11. In another embodiment, the degree of identity between the amino acid sequences encoded by SEQ ID NO: 1 or SEQ ID NO: 8 originating from Arabidopsis thaliana and an amino acid sequences from another plant, preferably a plant belonging to the superfamily Viridiplantae, is around 90% or 95%. Furthermore, all sequences whose transcription product is substantially identical to the amino acid sequences SEQ ID NO: 5 and SEQ ID NO: 11 according to this invention are included.

The amino acid sequences which are at least 30% identical to those coded by SEQ ID NO: 1 and SEQ ID NO: 8 are homologous sequences from A. thaliana or other organisms in which the protein for which they code has an equivalent function to the protein coded by the said MINIYO and RTR1 genes of plant origin, for example from Arabidopsis. The homologous sequences in general relate to sequences from different species originating from a common ancestral sequence. Two types of homology are generally distinguished in sequence homology: orthology and paralogy. Orthologous sequences belong to species which have a common past. Paralogous sequences are those which are found in the same organism and originate from duplication of a given gene. In one embodiment, the invention relates to any homologous sequences, including both orthologous and paralogous, which are at least 30% identical to the amino acid sequences encoded by SEQ ID NO: 1 or SEQ ID NO: 8, without prejudice to whether other sequences with lower degrees of identity with MINIYO and RTR1 are also regarded as being an object of the invention. The overall sequence identity is determined using a global alignment algorithm, for example the Needleman Wunsch algorithm in the program GAP (GCG Wisconsin Package, Accelrys), preferably with default parameters and preferably with sequences of mature proteins (i.e. without taking into account secretion signals or transit peptides) .

The orthologue may be selected from a MINIYO or RTR1 gene in any other plant, preferably a plant of superfamily Viridiplantae, in particular monocotyledonous and dicotyledonous plants, including forage plants and vegetables for livestock, ornamental plants, crop plants for use in human or animal nutrition and plants for use as bioenergy. Specific plants from which the ortholgue may be derived are listed elsewhere in this application as non-limiting examples of transgenic plants. In one embodiment of the various aspects of the invention, the MINIYO gene is selected from one of the following plants:

Oryza sativa (SEQ ID No. 12 peptide sequence, SEQ ID No. 18 nucleic acid sequence), Zea mays (SEQ ID No. 13 peptide sequence, SEQ ID No. 19 nucleic acid sequence), Glycine max (SEQ ID No. 14 and 15 peptide sequences, SEQ ID No. 20, 21 nucleic acid sequences), Brachypodium distachyon (SEQ ID No. 16 peptide sequence), Sorghum bicolor (SEQ ID No. 17 peptide sequence) .

In one embodiment of the various aspects of the invention, the RTR1 gene is selected from one of the following plants: Oryza sativa (SEQ ID No. 22 peptide sequence, SEQ ID No. 28 nucleic acid sequence), Zea mays (SEQ ID No. 23 peptide sequence, SEQ ID No. 29 nucleic acid sequence), Glycine max (SEQ ID No. 24, 25 peptide sequences, SEQ ID No. 30, 31 nucleic acid sequences), Brachypodium distachyon (SEQ ID No. 27 peptide sequence), Sorghum bicolor (SEQ ID No. 26 peptide sequence) .

As shown in figures 16 to 21, genes encoding for MINIYO and RTR1 in plants and their resulting proteins are conserved and show a number of conserved domains .

For the MINIYO protein, one of these domains is a glycine rich domain comprising an RGG element. This domain is located at position 960-980 in Arabidopsis AtMINIYO. Mutating G962E results in a partial loss of function mutant. Therefore, orthologues of AtMINIYO are characterised by the presence of a conserved glycine rich domain as shown in Figure 3b for MINIYO proteins from different species. Thus, orthologues proteins comprise a sequence which has at least 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% identity with the domain in Arabidopsis SEQ ID No. 32: RGGLAPGVGLGWGASGGGFWS . FIG. 18 (a). In addition, as shown in figure 18, orthologues are characterised by the presence of one or more further conserved domains which show a high degree of sequence identity, preferably at least 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% to the following domains in Arabidopsis:

amino acids 209-255 SEQ ID No. 33

SDIDVENHAKLQTMSPDEIAEAQAELLDKMDPALLS ILKKRGEAKLK . FIG 18 (b) ; amino acids 317-396 SEQ ID No. 34

RDLRFSFDGNVVEEDVVSPAETGGKWSGVESAAERDFLRTEGDPGAAGYTIKEAIAL ARSVI PGQRCLALHLLASVLDKA. FIG 18 (c) ;

amino acids 350-389 SEQ ID No. 35

ERDFLRTEGDPGAAGYTIKEAIALARSVIPGQRCLALHLL . FIG 18 (d) ; - amino acids 417-437 SEQ ID No. 36 DWEAIWAYALGPEPELVLALR . FIG 18 (e) . ;

amino acids 529-559 SEQ ID No. 37

TIQKDVFVAGQDVAAGLVRMDILPRIYHLLEE . FIG 18 ( f ) ;

- amino acids 529-597 SEQ ID No. 38

TIQKDVFVAGQDVAAGLVRMDILPRIYHLLEEPTAALEDS I I SVTIAIARHSPKCTTAILKY PKFVQT . FIG 18 (g) ;

- amino acids 1136-1145 SEQ ID No. 39 EWAHQRMPLP . FIG 18 (h) ; and/or

- amino acids SEQ ID No. 40 1144-1416

LPPHWFLSAI SAVHSGKTSTGPPESTELLEVAKAGVFFLAGLESSSGFGSLPSPVVSVPLVW KFHALSTVLLVGMDI IEDKNTRNLYNYLQELYGQFLDEARLNHRDTELLRFKSDIHENYSTF LEMVVEQYAAVSYGDVVYGRQVSVYLHQCVEHSVRLSAWTVLSNARVLELLPSLDKCLGE AD GYLEPVEENEAVLEAYLKSWTCGALDRAATRGSVAYTLVVHHFSSLVFCNQAKDKVSLRN KI VKTLVRDLSRKRHREGMMLDLLRYK. FIG 18 (i)

For the RTR1 protein, there is a conserved domain (DUF408) with a zinc-finger like motif located at the N-terminus of the protein that is found in all the orthologues from plants, animals and fungi. This domain is located at position 45-98 in Arabidopsis AtRTRl . The zinc-finger-like-motif has been implicated in interaction with the RNA Polymerase II C- terminal domain (CTD) and the Integrator complex in humans and is required for CTD-phosphatase activity in yeast and humans (Mosley et al . , 2009; Egloff et al . , 2011). Interestingly, this motif is also required for interaction of RTR1 with IYO. Substituting the putative zinc coordinating cysteine residues (C56A/C61A or C94A/C98A) in the full-length AtRTRl protein for alanine abrogates interaction with IYO. Intriguingly, however, both the truncated N-terminal and the C-terminal halves of RTR1 can interact with IYO, suggesting that although RTR1 binds at both ends of the protein to IYO, it requires an intact zinc-finger-like motif in the context of the full length protein for binding.

A consensus sequence for the zinc-finger like motif derived from sequences from multicellular eukaryotes is (the putative Zinc-coordinating cysteines are highlghted in bold) : D [IV] V [TDEV] ER [ASTF] I [AVIS] [KND] [LAV] CGY [TP] [ LRA] CXXXLX ₇ _

is [YF] [RK]IS[LT] [KSR] [TAED] [HKN] [KR] VYD [ IL ] [ THEQ ] EXXX [FY] CXXXC A blast search against the non-redundant protein sequence database at NCBI with the corresponding sequence from Arabidopsis

DVVTERAIAKLCGYTLCQRFLPSDVSRRGKYRI SLKDHKVYDLQETSKFCSAGC SEQ ID

No. 41 retrieved the RTR1 orthologues from plants, animals and fungi with a low E-value (< 1CT ⁶ ) .

Therefore, orthologues of AtRTRl from plants animals and fungi are characterised by the presence of a conserved zinc-finger like motif as shown in Figure 21. Thus, orthologues proteins comprise a sequence which has at least 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% identity with the domain in Arabidopsis SEQ ID No. 42:

DVVTERAIAKLCGYTLCQRFLPSDVSRRGKYRI SLKDHKVYDLQETSKFCSAGC . FIG. 21 (a) .

In addition, orthologues to the AtRTRl Arabidopsis protein are characterised by the presence of one or more further conserved domains as shown in figure 21, which show a high degree of sequence identity, preferably at least 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% to the following domains in Arabidopsis:

- amino acids 39-61 SEQ ID No. 43 SRSDYEDVVTERAIAKLCGYTLC . This domain includes catalytic cysteine C56 which is strictly conserved in all the orthologues. FIG. 21 (b) .

- amino acids. 77-89 SEQ ID No. 44 ISLKDHKVYDLQE . FIG. 21 (c);

- amino acids. 429-435 SEQ ID No. 45 SVTWADQ . FIG. 21 (d) ; ;

amino acids 473-507 SEQ ID No. 46 AEALATALSQAAEAVSSGNSDASDATAKAGI ILLP . FIG. 21 (e);

and/or

amino acids 552-589 SEQ ID No. 47.

SWFDGPPEGFNLTLSNFAVMWDSLFGWVSSSSLAYIYG. FIG. 21 (f) Thus, a skilled person would understand that MINIYO and RTR1 are highly conserved in plants and characterised by the presence of the conserved domains above. Accordingly, the MINIYO and RTRl proteins according to the invention can be defined and identified through the presence of these domains set out herein, in particular with reference to figures 18 and 21. A skilled person would therefore be able to identify orthologues to AtMINIYO and ATRTR1 by reference to these domains through routine methods.

Another aspect of the invention relates to an expression vector which comprises one or more isolated nucleic acid molecule (s) of the invention. The invention also relates to the use of an expression vector as described herein to control the initiation of cell differentiation in the apical, root floral and/or other meristems of a plant. The term "vector" refers to a fragment of DNA which has the ability to replicate in a given host and, as the term indicates, it can act as a vehicle to multiply another DNA fragment which has been fused to it ("insert") . "Insert" refers to a fragment of DNA fused to the vector; in the case of this invention the vector may comprise any of the sequences described in accordance with the aspects of the invention which, when fused to the same, can replicate in a suitable host. The vectors may be plasmids, cosmids, bacteriophages or lentiviral vectors suitable for transforming or transfecting fungal or animal cells, without excluding other kinds of vectors which correspond to the definition of vector provided.

Expression of the said nucleic acid molecules may be under the control of a promoter sequence. The promoter used in the gene constructs of the vectors described above to express MINIYO or RTRl may be an endogenous MINIYO or RTRl promoter, for example the AtMINIYO or AtRTRl promoter (SEQ Id No 48 and 49) or a MINIYO or RTRl promoter from a AtMINIYO or AtRTRl orthologue. Alternatively, the promoter may regulate overexpression of the gene. Overexpression according to the invention means that the transgene is expressed at a level that is higher than expression of endogenous counterparts (MINIYO or RTRl) driven by their endogenous promoters. For example, overexpression may be carried out using a strong promoter, such as the cauliflower mosaic virus promoter (CaMV35S), the rice actin promoter or the maize ubiquitin promoter or any promoter that gives enhanced expression.

Alternatively, an inducible expression system may be used, where expression is driven by a promoter induced by environmental stress conditions (for example the pepper pathogen-induced membrane protein gene CaPIMPI or promoters that comprise the dehydration-responsive element (DRE) , the promoter of the sunflower HD-Zip protein gene Hahb4 or Hahbl, which is inducible by water stress, high salt concentrations and ABA, or a chemically inducible promoter (such as steroid- or ethanol-inducible promoter system) . Such promoters are described in the art. Other suitable promoters and inducible systems are also known to the skilled person.

As a skilled person will know, the expression vector may also comprise a selectable marker which facilitates the selection of transformants , such as a marker that confers resistance to antibiotics, such as kanamycin.

In any of the expression vectors described herein, wild type sequences that encode MINIYO or RTR1 polypeptides can be included, but in one embodiment, variant sequence or fragments may also be used, provided such sequences encode a polypeptide that has the same biological activity as the wild type sequence. Sequence variations in the wild type sequence include silent base changes that do not lead to a change in the encoded amino acid sequence and/or base changes that affect the amino acid sequence, but do not affect the biological activity of the polypeptide. Changes may be conservative amino acid substitutions, i.e. a substitution of one amino acid residue where the two residues are similar in properties. Thus, variant/mutant polypeptides encoded by such sequences retain the biological activity of the wild type polypeptide and act on cell differentiation. In another embodiment, mutant sequence or fragments may also be used, which encode a polypeptide that has a different biological activity as the wild type sequence. These modifications are described below.

A sequence or vector described herein encoding for the MINIYO or RTR1 protein is introduced as a transgene into the plant. This can be carried out by various methods as known in the field of plant genetic engineering, for example using transformation with Agrobacterium or particle bombardment.

Another embodiment of the invention relates to a host cell which comprises the expression vector of the invention.

The term "cell" as understood in this invention relates to a prokaryotic or eukaryotic cell. The cell may be a bacterium capable of replicating a transformed foreign DNA such as for example any of the strains of the species Escherichia coli. Preferably cell refers to a eukaryotic fungal, plant or animal cell. Thus, in the case where the cell is a fungus, the term cell comprises at least an individual cell of a yeast, a mycelium of a filamentous fungus, or other fungal cell of any type, whether germinal (spore) or vegetative, differentiated or undifferentiated. In the case of an animal cell it may be any normal or tumour cell line, from any tissue or organ, adult or embryonal, multipotent (undifferentiated) or differentiated. Likewise a protoplast (a fungal cell without a cell wall) is also included in this definition.

The invention also includes a method for generating of transgenic plants which constitutively or conditionally express or over-express a nucleic acid of the invention, that is a nucleic acid that encodes for a plant MINIYO and/or RTR1 protein, throughout the plant or in specific meristems, to advance the onset of differentiation, reducing the size of the meristems or eliminating them, depending upon the level of over-expression obtained. It also includes the over-expression of mutated versions of MINIYO and/or RTR1 which are not excluded from the nucleus in undifferentiated cells. In one aspect of the invention, mutated constructs of MINIYO and/or RTRl that are retained in the cytosol or in the nucleus are expressed under constitutive, inducible, tissue-specific or developmental-stage-specific promoters, to modify specifically cell proliferation or cell differentiation rates in different meristems and during embryogenesis . These constructs are described below.

The invention also includes a method for generating transgenic plants in which a nucleic acid of the invention that encodes for a plant MINIYO and/or RTRl protein is expressed throughout the plant or in specific meristems, to delay the onset of differentiation. Such nucleic acids include mutated constructs of MINIYO and/or RTRl as described herein. These methods include introducing an nucleic acid of the invention into said plant by means of recombinant DNA technology and expressing said transgene in the plant.

In another aspect, the invention relates to a transgenic plant wherein the activity of a MINIYO polypeptide as described herein is inactivated, repressed or down-regulated. As described above, said MINIYO protein is at least 30% identical to the sequences coded by SEQ ID NO : 1. In one embodiment, the MINIYO protein comprises or consists of SEQ ID No. 5. Thus, in another aspect, the invention relates to a transgenic plant wherein the activity of a RTRl polypeptide as described herein is inactivated, repressed or down-regulated. As described above, said RTRl protein is at least 30% identical to the sequences coded by SEQ ID NO : 8. In one embodiment, the RTRl protein comprises or consists of SEQ ID No. 11.

In one embodiment, the transgenic plant may be characterised in that activity of both a MINIYO and RTRl polypeptide as described herein is inactivated, repressed or down-regulated.

In another embodiment, RNA-mediated gene suppression or RNA silencing may be used to achieve silencing of the MINIYO or RTR1 gene. "Gene silencing" is a term generally used to refer to suppression of expression of a gene via sequence-specific interactions that are mediated by RNA molecules. The degree of reduction may be so as to totally abolish production of the encoded gene product, but more usually the abolition of expression is partial, with some degree of expression remaining. The term should not therefore be taken to require complete "silencing" of expression. Transgenes may be used to suppress endogenous plant genes. This was discovered originally when chalcone synthase transgenes in petunia caused suppression of the endogenous chalcone synthase genes and indicated by easily visible pigmentation changes. Subsequently it has been described how many, if not all plant genes can be "silenced" by transgenes. Gene silencing requires sequence similarity between the transgene and the gene that becomes silenced. This sequence homology may involve promoter regions or coding regions of the silenced target gene. When coding regions are involved, the transgene able to cause gene silencing may have been constructed with a promoter that would transcribe either the sense or the antisense orientation of the coding sequence RNA. It is likely that the various examples of gene silencing involve different mechanisms that are not well understood. In different examples there may be transcriptional or post transcriptional gene silencing and both may be used according to the methods of the invention.

RNA-mediated gene suppression or RNA silencing according to the methods of the invention includes co-suppression wherein over-expression of the MINIYO or RTR1 gene sense RNA or mRNA leads to a reduction in the level of expression of the genes concerned. RNAs of the transgene and homologous endogenous gene are co-ordinately suppressed.

Other techniques used in the methods of the invention include antisense RNA to reduce transcript levels of the endogenous MINIYO and/or RTR1 gene in a plant. In this method, RNA silencing does not affect the transcription of a gene locus, but only causes sequence-specific degradation of target mRNAs . An "antisense" nucleic acid sequence comprises a nucleotide sequence that is complementary to a "sense" nucleic acid sequence encoding a MINIYO and/or RTR1 protein, or a part of a MINIYO and/or RTR1 protein, i.e. complementary to the coding strand of a double-stranded cDNA molecule or complementary to an mRNA transcript sequence. The antisense nucleic acid sequence is preferably complementary to the endogenous MINIYO and/or RTR1 gene to be silenced. The complementarity may be located in the "coding region" and/or in the "non-coding region" of a gene. The term "coding region" refers to a region of the nucleotide sequence comprising codons that are translated into amino acid residues. The term "non-coding region" refers to 5' and 3' sequences that flank the coding region that are transcribed but not translated into amino acids (also referred to as 5' and 3' untranslated regions) .

The length of a suitable antisense oligonucleotide sequence is known in the art and may start from about 50, 45, 40, 35, 30, 25, 20, 15 or 10 nucleotides in length or less. An antisense nucleic acid sequence according to the invention may be constructed using chemical synthesis and enzymatic ligation reactions using methods known in the art.

Antisense nucleic acid sequences may be introduced into a plant by transformation or direct injection at a specific tissue site. Alternatively, antisense nucleic acid sequences can be modified to target selected cells and then administered systemically . For example, for systemic administration, antisense nucleic acid sequences can be modified such that they specifically bind to receptors or antigens expressed on a selected cell surface, e.g., by linking the antisense nucleic acid sequence to peptides or antibodies which bind to cell surface receptors or antigens. The antisense nucleic acid sequences can also be delivered to cells using vectors. RNA interference (RNAi) is another post-transcriptional gene- silencing phenomenon which may be used according to the methods of the invention. This is induced by double-stranded RNA in which mRNA that is homologous to the dsRNA is specifically degraded.

Thus, a plant may be transformed to introduce a RNAi, snRNA, dsRNA, siRNA, miRNA, ta-siRNA or cosuppression molecule that has been designed to target the expression of the MINIYO and/or RTR1 gene and selectively decreases or inhibits the expression of the gene or stability of its transcript. Preferably, the RNAi, snRNA, dsRNA, siRNA, miRNA, ta-siRNA or cosuppression molecule used in the methods of the invention comprises a fragment of at least 17 nt, preferably 22 to 26 nt and can be designed on the basis of the information shown in SEQ ID No. 1 and/or 8. Guidelines for designing effective siRNAs are known to the skilled person. siNA molecules may be double stranded. In one embodiment, double stranded siNA molecules comprise blunt ends. In another embodiment, double stranded siNA molecules comprise overhanging nucleotides (e.g., 1-5 nucleotide overhangs, preferably 2 nucleotide overhangs) . In some embodiments, the siRNA is a short hairpin RNA (shRNA); and the two strands of the siRNA molecule may be connected by a linker region (e.g., a nucleotide linker or a non-nucleotide linker) . The siNAs of the invention may contain one or more modified nucleotides and/or non-phosphodiester linkages. Chemical modifications well known in the art are capable of increasing stability, availability, and/or cell uptake of the siNA. The skilled person will be aware of other types of chemical modification which may be incorporated into RNA molecules. In one embodiment, recombinant DNA constructs as described in US 6635805, incorporated herein by reference, may be used.

Silencing of the MINIYO and/or RTR1 gene may also be achieved using virus-induced gene silencing. For example, the transgenic plant having reduced activity of the MINIYO and/or RTRl polypeptides may be characterised in that in comparison with the wild phenotype plant said plant has a reduction of between 50% and 100% in the expression of a gene encoding for an amino acid sequence of the MINIYO and/or RTRl protein as described herein.

In one embodiment, the endogenous MINIYO or RTRl gene carries a functional mutation.

In another embodiment, the transgenic plant expresses a transgene said transgene comprising a modified MINIYO or RTRl nucleic acid sequence when compared to a wild type sequence. For example, said modification/functional mutation of the MINIYO nucleic acid sequence results in a polypeptide comprising a substitution of the second conserved G in the RGG motif (SEQ ID No. 32) . With reference to the Arabidopsis sequence, this is G962E. The numbering of the amino acid residues as used in this disclosure is based on the numbering of the Arabidopsis AtMINIYO . Because the MINIYO or RTRl amino acid sequence in other species may comprise fewer or more amino acids, the position of the second conserved G in the RGG motif residue may not be 962, but may between position 947 to 1067 (Fig. 16) . The positions of the targeted residues according to the invention in some exemplified plant species are shown in figure 3B.

In another embodiment, the modification is a substitution or deletion of one or more residues within the nuclear localisation signals present in the MINIYO and/or RTRl protein. In another embodiment, it is an insertion.

MINIYO and RTRl are required for cell proliferation in meristematic cells, where they accumulate primarily in the cytosol, albeit shuttling through the nucleus, as evidenced by the fast nuclear accumulation when export is blocked with leptomycin B. Moreover, in the meristem periphery, MINIYO accumulates in the nucleus and together with RTR1 switches on cell differentiation. The shuttling between the cytosol and the nucleus implies that MINIYO and RTR1 have domains responsible for nuclear import and for nuclear export. Those signals can be identified through a blind genetic search, testing the localization of mutant versions of the proteins (i.e: a deletion series), or by a directed bioinformatic search for nuclear localization signals (NLS) and nuclear export signals (NES) in the protein sequences. Those skilled in the art will be aware that by mutating the domains required for nuclear import or nuclear export, it is possible to generate MINIYO and RTR1 constructs such that the encoded proteins are retained in the cytosol or in the nucleus, respectively. In this way, the two activities of MINIYO and RTR1 (promoting cell proliferation and promoting cell differentiation) may be uncoupled. Constructs that cause retention of MINIYO and RTR1 in the cytosol may specifically promote proliferation without affecting the timing of differentiation, whereas the constructs that cause MINIYO and RTR1 to be retained in the nucleus will specifically promote cell differentiation. The predicted NLS in AtMINIYO are located at aa. 250-262 (GEAKLKKRKHSVQ, SEQ ID No. 50) and at aa . 1397-1420 (RDLSRKRHREGMMLDLLRYKKGSA, SEQ ID No. 51) .

Thus, the invention relates to a nucleic acid construct comprising a MINIYO nucleic acid sequence which encodes for a polypeptide that has a mutation in one of both of the NLS of the resulting MINIYO polypeptide. The mutation may be a substitution or deletion of one or more residues in the NLS, preferably all residues. In one embodiment, residues aa. 250- 262 and/or aa. 1397-1420 in AtMINIYO or corresponding residues in orthologues are deleted. Said construct may be introduced and expressed in a transgenic plant according to the methods of the invention to exclude the MINIYO polypeptide from the cell nucleus and thus block cell differentiation and stimulate cell proliferation. Using inducible promoters, the nucleic acid may be included in an expression vector as described herein so that the timing of the expression can be specifically determined.

In one embodiment of the invention, an MINIYO protein impaired in nuclear import is expressed under the control of an embryo specific promoter (such as the Arabidopsis cruciferin promoter, the Brassica napus Napin A promoter, the rice glutelin promoter, the maize 19 Kda zein promoter, the wheat SPA promoter or the pea legumin promoter) or an endosperm- specific promoter (such as the wheat gliadin promoter, the rice prolamin promoter, or the maize END promoter) to increase cell proliferation, seed size and yield in a seed crop.

In another embodiment of the invention, an MINIYO protein impaired in nuclear import is expressed under the control of a shoot meristem promoter (such as KNOX gene promoters from Brassica, rice or maize) to increase cell proliferation, meristem size, meristem number, production of aerial organs and crop yield (leaves, flowers) .

In one embodiment of the invention, an MINIYO protein impaired in nuclear import is expressed under the control of axillary bud specific promoter (BRC1 promoter from Arabidopsis, TBI promoter from maize, OSTB1 promoter from rice, ATC085 promoter from tobacco, SlBRCla and SIBRClb promoters from tomato) to increase branching and yield.

In one embodiment of the invention, an MINIYO protein impaired in nuclear import is expressed under the control of a root meristem specific promoter (RCH1 promoter, the brassica Gl-3b promoter) to increase cell proliferation, root growth, nutrient uptake and plant yield.

In one embodiment of the invention, an MINIYO protein impaired in nuclear import is expressed under the control of the IYO promoter that is active in embryos and in plant meristems, to increase seed size, meristem size, plant growth and improve yields in target crops.

The predicted NLS in AtRTRl is located at aa. 340-368. LKGDLQTLDGKNTLSGSSSGSNTKGSKTK, SEQ ID No.52.

Thus, the invention relates to a nucleic acid construct comprising a RTR1 nucleic acid sequence which encodes for a polypeptide that has a mutation in the NLS of the resulting RTR1 polypeptide. The mutation may be a substitution or deletion of one or more residues in the NLS, preferably all residues. Said construct may be introduced and expressed in a transgenic plant according to the methods of the invention to exclude the RTR1 polypeptide from the cell nucleus and thus block cell differentiation and stimulate cell proliferation. Using inducible promoters, the nucleic acid may be included in a an expression vector as described herein so that the timing of the expression can be specifically determined. In one embodiment of the invention, an RTR1 protein impaired in nuclear import is expressed under the control of an embryo specific promoter (such as the Arabidopsis cruciferin promoter, the Brassica napus Napin A promoter, the rice glutelin promoter, the maize 19 Kda zein promoter, the wheat SPA promoter or the pea legumin promoter) or an endosperm- specific promoter (such as the wheat gliadin promoter, the rice prolamin promoter, or the maize END promoter) to increase cell proliferation, seed size and yield in a seed crop.

In another embodiment of the invention, an RTR1 protein impaired in nuclear import is expressed under the control of a shoot meristem promoter (such as KNOX gene promoters from Brassica, rice or maize) to increase cell proliferation, meristem size, meristem number, production of aerial organs and crop yield (leaves, flowers) . In one embodiment of the invention, an RTR1 protein impaired in nuclear import is expressed under the control of a root meristem specific promoter (RCH1 promoter, the brassica Gl-3b promoter) to increase cell proliferation, root growth, nutrient uptake and plant yield.

In one embodiment of the invention, an RTR1 protein impaired in nuclear import is expressed under the control of the MINIYO promoter, active in embryos and in plant meristems, to increase seed size, meristem size, plant growth and improve yields in target crops.

Also within the scope of the invention are transgenic plants wherein both the MINIYO protein and the RTR1 are impaired in nuclear import. Combinations of the manipulations of the NLS in MINIYO protein and the RTR1 as set out above can be used to achieve this.

The activity of RTR1 may also be decreased by manipulating the interaction between MINIYO and RTR1 proteins. This can achieved by manipulating certain residues in the MINIYO and/or RTR1 polypeptide sequences. For example, substituting the putative zinc coordinating cysteine residues for alanines (C56A/C61A or C94A/C98A in the Arabidopsis sequence) in the full-length AtRTRl protein abrogates the interaction with MINIYO.

Another aspect of the invention refers to a transgenic plant wherein the activity of a MINIYO polypeptide is increased or up-regulated. Another aspect of the invention refers to a transgenic plant wherein the activity of a RTR1 polypeptide is increased or up-regulated.

In one embodiment, the transgenic plant is characterised in that the activity of both a MINIYO and a RTR1 polypeptides is increased or up-regulated in the same plant.

For example, said plant overexpresses a nucleic acid encoding for a MINIYO protein that is at least 30% identical to the sequences coded by SEQ ID NO : 1. In another embodiment, said plant overexpresses a nucleic acid encoding for a RTR1 protein that is at least 30% identical to the sequences coded by SEQ ID NO: 8.

In another embodiment, said plant expresses a transgene said transgene comprising a modified MINIYO and a RTRl nucleic acid sequence when compared to a wild type sequence.

For example, said modification is a substitution or deletion of one or more residues within the nuclear export signal present in the MINIYO or RTRl protein.

Preferably, over-expression will be between 2 and 100 times the expression of the endogenous mRNA. One way of increasing the activity of MINIYO or RTRl is to retain the protein in the nucleus.

The predicted NES in AtMINIYO is located at 432-440. LVLALRMAL SEQ ID No. 53.

Thus, the invention relates to a nucleic acid construct comprising a MINIYO nucleic acid sequence which encodes for a polypeptide that has a mutation in the NES of the resulting MINIYO polypeptide. The mutation may be a substitution or deletion of one or more, preferably all residues of the NES. In one embodiment, residues 432-440 in AtMINIYO or corresponding residues in orthologues are deleted. Said construct may be introduced and expressed in a transgenic plant according to the methods of the invention to retain the MINIYO polypeptide in the cell nucleus and stimulate cell differentiation. Using inducible promoters, the nucleic acid may be included in a an expression vector as described herein so that the timing of the expression of the mutated nucleic acid can be specifically determined.

In one embodiment of the invention, a MINIYO protein impaired in nuclear export is expressed under the control of axillary bud specific promoter (BRC1 promoter from Arabidopsis, TBI promoter from maize, 0STB1 promoter from rice, ATC085 promoter from tobacco, SlBRCla and SIBRClb promoters in tomato) to reduce branching and increase yield. This is particularly important for forestry applications, for instance for growing closely packed trees used for pulp production in the paper or biofuel industry.

In one embodiment of the invention, a MINIYO protein impaired in nuclear export is expressed under the control of an inflorescence meristem specific promoter (such as the LFY promoter) to terminate the inflorescence meristem in crops that are cultivated for their vegetative organs and in which flowering reduces the harvest (lettuce, spinach, sugar beet, potato, and others) .

The predicted NES in RTR1 is located at 340-349 (LKGDLQTLDG, SEQ ID No .54) .

Thus, the invention relates to a nucleic acid construct comprising a RTR1 nucleic acid sequence which encodes for a polypeptide that has a mutation in the NES of the resulting RTR1 polypeptide. The mutation may be a substitution or deletion of one or more, preferably all residues of the NES. In one embodiment, residues 432-440 are deleted. Said construct may be introduced and expressed in a transgenic plant according to the methods of the invention to retain the RTR1 polypeptide in the cell nucleus and stimulate cell differentiation. Using inducible promoters, the nucleic acid may be included in an expression vector as described herein so that the timing of the expression of the mutated nucleic acid can be specifically determined.

Also within the scope of the invention are transgenic plants wherein both the MINIYO protein and the RTR1 are impaired in nuclear import. Combinations of the manipulations of the NLS in MINIYO protein and the RTR1 as set out above can be used to achieve this. In one aspect, the invention relates to transgenic plants wherein both, MINIYO and RTR1 have been manipulated. As shown in the examples, MINIYO and RTR1 are jointly responsible for the control of cell differentiation, supporting a close functional interaction. Differentiation in the iyo-latrtrl-2 double mutants was almost completely blocked and the plants eventually developed as a friable callus of undifferentiated cells. This phenotype is much stronger than the sum of the phenotypes of the single mutants. Thus, transgenic plants according to the invention may have reduced or increased activity for both, MINIYO and RTR1 by manipulating activity of MINIYO and RTR1 as explained herein.

For the purposes of the invention, "transgenic", "transgene" or "recombinant" means with regard to, for example, a nucleic acid sequence, an expression cassette, gene construct or a vector comprising the nucleic acid sequence or an organism transformed with the nucleic acid sequences, expression cassettes or vectors according to the invention, all those constructions brought about by recombinant methods in which either

(a) the nucleic acid sequences encoding proteins useful in the methods of the invention, or

(b) genetic control sequence (s) which is operably linked with the nucleic acid sequence according to the invention, for example a promoter, or

(c) a) and b)

are not located in their natural genetic environment or have been modified by recombinant methods, it being possible for the modification to take the form of, for example, a substitution, addition, deletion, inversion or insertion of one or more nucleotide residues. The natural genetic environment is understood as meaning the natural genomic or chromosomal locus in the original plant or the presence in a genomic library. In the case of a genomic library, the natural genetic environment of the nucleic acid sequence is preferably retained, at least in part. The environment flanks the nucleic acid sequence at least on one side and has a sequence length of at least 50 bp, preferably at least 500 bp, especially preferably at least 1000 bp, most preferably at least 5000 bp. A naturally occurring expression cassette - for example the naturally occurring combination of the natural promoter of the nucleic acid sequences with the corresponding nucleic acid sequence encoding a polypeptide useful in the methods of the present invention, as defined above - becomes a transgenic expression cassette when this expression cassette is modified by non-natural, synthetic ("artificial") methods such as, for example, mutagenic treatment. Suitable methods are described, for example, in US 5,565,350 or WO 00/15815 incorporated by reference .

A transgenic plant for the purposes of the invention is thus understood as meaning, as above, that the nucleic acids used in the method of the invention are not at their natural locus in the genome of said plant, it being possible for the nucleic acids to be expressed homologously or heterologously . However, as mentioned, transgenic also means that, while the nucleic acids according to the different embodiments of the invention are at their natural position in the genome of a plant, the sequence has been modified with regard to the natural sequence, and/or that the regulatory sequences of the natural sequences have been modified. Transgenic is preferably understood as meaning the expression of the nucleic acids according to the invention at an unnatural locus in the genome, i.e. homologous or, preferably, heterologous expression of the nucleic acids takes place. Preferred transgenic plants are mentioned herein.

Transgenic plants according to the invention display altered cell differentiation and proliferation compared to a control plant. A control plant according to the invention is a plant that is not modified in the same way as the transgenic plant of the invention with respect to MINIYO and/or RTR1 expression or polypeptide activity. In one embodiment, this plant is a wild type plant. In another embodiment, this plant is a parent plant that may comprise additional modifications through expression of other transgene of interest that modify desired pathways, for example stress resistance.

The MINIYO or RTR1 genes according to the different aspects of the invention may be an exogenous gene, such as Arabidopsis AtMINIYO or AtRTRl , overexpressed in a different plant species. Alternatively, the MINIYO or RTR1 may be an endogenous plant gene, i.e. a gene that is endogenous to the plant in which it is introduced via recombinant methods and (over) -expressed.

In a preferred embodiment of the invention, the transgenic plant is characterised in that it is selected from the group comprising: plants for particular use in the methods according to the invention include all the plants belonging to the superfamily Viridiplantae, in particular monocotyledonous and dicotyledonous plants including forage plants and vegetables for livestock, ornamental plants, crop plants for use in human or animal nutrition, plants for use as bioenergy, trees, and bushes selected from the list comprising: Acer spp . , Actinidia spp., Abelmoschus spp., Agropyron spp., Allium spp., Amaranthus spp., Ananas comosus, Annona spp., Apium graveolens, Arabidopsis thaliana, Arachis spp, Artocarpus spp., Asparagus officinalis, Avena sativa, Averrhoa carambola, Benincasa hispida, Bertholletia excelsea, Beta vulgaris, Brachypodium spp., Brassica spp., Cadaba farinosa, Camellia sinensis, Camelina spp., Canna indica, Capsicum spp., Carex elata, Carica papaya, Carissa macrocarpa, Carya spp., Carthamus tinctorius, Castanea spp., Cichorium endivia, Cinnamomum spp., Citrullus lanatus, Citrus spp., Cocos spp., Coffea spp., Colocasia esculenta, Cola spp., Coriandrum sativum, Corylus spp., Crataegusspp . , Crocus sativus, Cucurbita spp., Cucumis spp., Cynara spp., Daucus carota, Desmodium spp., Dimocarpus longan, Dioscorea spp., Diospyros spp., Echinochloa spp., Eleusine coracana, Eriobotrya japonica, Eucalyptus spp., Eugenia uniflora, Fagopyrum spp., Fagus spp., Ficus carica, Fortunella spp., Fragaria spp., Ginkgo biloba, Glycine spp., Gossypium hirsutum, Helianthus spp . , Hemerocallis fulva, Hibiscus spp . , Hordeum spp., Ipomoea batatas, Juglans spp., Jatropha spp., Lactuca sativa, Lathyrus spp., Lens culinaris, Linum usitatissimum, Litchi chinensis, Lotus spp., Luffa acutangula, Lupinus spp., Luzula sylvatica, Macrotyloma spp., Malus spp., Malpighia emarginata, Mammea americana, Mangifera ino!ica, Manihot spp., Manilkara zapota, Meo!icago sativa, Melilotus spp., Mentha spp., Momoro!ica spp., Morus nigra, Musa spp., Nicotiana spp., Olea spp., Opuntia spp., Ornithopus spp., Oryza spp., Panicum miliaceum, Passiflora edulis, Pastinaca sativa, Persea spp., Petroselinum crispum, Phaseolus spp., Phoenix spp., Physalis spp., Pistacia vera, Pisum spp., Poa spp., Populus spp., Prosopis spp., Prunus spp., Psidium spp., Punica granatum, Pyrus communis, Quercus spp., Raphanus sativus, Rheum rhabarbarum, Ribes spp., Ricinus communis, Saccharum spp., Sambucus spp., Secale cereale, Sesamum spp., Sinapis sp . , Solanum spp., Sorghum bicolor, Spinacia spp., Syzygium spp., Tamarindus indica, Theobroma cacao, Trifolium spp., Triticosecale rimpaui, Triticum spp., Tropaeolum minus, Tropaeolum majus, Vaccinium spp., Vicia spp., Vigna spp., Viola odorata, Vitis spp., Zea mays, Zizania palustris, Ziziphus spp., among others.

According to a preferred embodiment of the invention, the crop plant is a plant such as tomato, potato, pepper, fruiting plants of the prunus and citrus genuses, Jatropha curcas, soya, sunflower, rape, alfalfa, canola, cotton, brassica genuses or tobacco. Even more preferably, the plant is a monocotyledonous one such as sugar cane, and even more preferably a cereal such as rice, maize, wheat, rye, barley, millet, sorghum or oats. Most preferred plants are maize, rice, wheat, sorghum, canola and cotton.

Another preferred embodiment of the invention relates to a product obtained from the transgenic plant as described above, the said product being selected from seeds, stones, leaves, flowers, roots, flour and fruit. In a more preferred embodiment the said product is a transgenic seed. In one embodiment the products produced by said methods of the invention are plant products such as, but not limited to, a foodstuff, feedstuff, a food supplement, feed supplement, fiber, cosmetic or pharmaceutical. Foodstuffs are regarded as compositions used for nutrition or for supplementing nutrition. Animal feedstuffs and animal feed supplements, in particular, are regarded as foodstuffs. In another embodiment the inventive methods for the production are used to make agricultural products such as, but not limited to, plant extracts, proteins, amino acids, carbohydrates, fats, oils, polymers, vitamins, and the like. It is possible that a plant product consists of one ore more agricultural products to a large extent . The invention also relates to a method for generating a transgenic plant with altered cell differentiation and cell proliferation comprising altering the activity of a gene encoding a MINIYO polypeptide. This may be achieved by expressing a MINIYO transgene in a plant so that activity is altered. In another aspect, the invention relates to a method for generating a transgenic plant with altered cell differentiation and cell proliferation comprising altering the activity of a gene encoding a RTR1 polypeptide as defined herein. In another aspect, plants are generated where the activity of both, MINIYO and RTR1, is manipulated. As explained elsewhere, alteration of the activity of MINIYO and/or RTR1 means that the activity may be increased or decreased. This may be achieved by manipulating the NLS/NES sequences and introducing constructs that express MINIYO and/or RTR1 proteins modified in this way as explained herein. Other ways of manipulating the activity of MINIYO and RTR1, such as gene silencing or the generation of partial loss of function mutants, are also set out herein. In another aspect, the invention relates to a plant obtained/obtainable by said methods. In another aspect, the invention relates to a method for altering localisation of MINIYO and/or RTRl in a plant by manipulating the NLS/NES sequences of MINIYO and/or RTRl as described herein. In this way, MINIYO and/or RTRl may be retained or excluded from the nucleus in one or more meristems. The NLS/NES sequences can be manipulated to achieve this as set out herein and transgenes carrying such manipulations can be introduced and expressed in a plant. In another aspect, the invention also relates to a method for improving the architecture and yield of plants through genetic changes to the MINIYO (SEQ ID No 1), AtRTRl (SEQ ID No 8) genes or their orthologues in other plants. The expression of improving architecture refers to the non-exclusive list of altering the size/number of one or more meristems, altering the number of side branches, altering inflorescence, altering thickness of the stems, modify thickness of the stems and increasing plant yield. In a preferred embodiment of the method for improving the architecture and yield of plants, the method is used to alter the size of one or more meristems, including increasing or decreasing the activity of the MINIYO and RTRl genes. In a preferred embodiment of the method, it is used to increase the size of the meristems by delaying the onset of differentiation and consequently increasing the number of undifferentiated cells brought about through the loss of function of MINIYO and/or RTRl. Preferably, to obtain ectopic shoot apical meristems through delaying the onset of differentiation and the consequent increase in the number of undifferentiated cells caused by the loss of function of MINIYO and/or RTRl. In another preferred embodiment of the improving the architecture and yield of plants, the method is to obtain ectopic floral meristems through delaying the onset of differentiation and the consequent increase in the number of undifferentiated cells caused by the loss of function of MINIYO and/or RTR1.

In another preferred embodiment of the method, it is used to obtain ectopic root meristems through delaying the onset of differentiation and the consequent increase in the number of undifferentiated cells caused by the loss of function of MINIYO and/or RTR1. In another preferred embodiment, the method is to obtain ectopic embryos through delaying the onset of differentiation in the suspensor cells caused through the loss of function of MINIYO and/or RTR1. In a preferred embodiment, the method is used to reduce or eliminate meristems through delaying the onset of differentiation caused by the increased activity of MINIYO and/or RTR1. Preferably, to reduce the number of side branches in crops through increasing the activity of MINIYO and/or RTR1, specifically in axillary buds.

In another preferred embodiment, the method is used to compact inflorescence through increasing the activity of MINIYO and/or RTR1 in reproductive meristems.

In another preferred embodiment, the thickness of the stems of herbaceous plants is increased.

In another preferred embodiment, secondary growth in shrubs is modified.

In another more aspect, the invention includes a method to increase plant yield by decreasing or downregulating the activity of MINIYO and/or RTR1 in a transgenic plant. This may be achieved as described elsewhere, including through manipulating of the NLS sequences, creating mutant proteins that lead to partial loss of function or gene silencing. Another preferred embodiment of the invention relates to the development of transgenic plants for use in obtaining biofuels, such as in the production of bioethanol. The invention also relates to the use of a polypeptide having at least 30% sequence identity to a polypeptide encoded by SEQ ID NO. 1 or 8 in altering cell differentiation, cell proliferation, meristem formation/growth and/or increasing crop yield.

In another aspect, the invention relates to manipulating the interaction between MINIYO and RTR1 proteins, . This can achieved by manipulating certain residues in the MINIYO and/or RTR1 polypeptide sequences. For example, substituting the putative zinc coordinating cysteine residues for alanines (C56A/C61A or C94A/C98A in the Arabidopsis sequence) in the full-length AtRTRl protein abrogates the interaction with MINIYO.

In another embodiment, the invention relates to an isolated nucleic acid sequence comprising or consisting of SEQ ID No. 48 (AtMINIYO promoter) . In another embodiment, the invention relates to an isolated nucleic acid sequence comprising or consisting of SEQ ID No. 49 (RTR1 promoter). Such promoter sequences may be fused to any gene of interest to direct spatial and temporal expression of the target gene. The invention also relates to the use of these promoter sequence in directing expression at sites of active cell proliferation and differentiation (for example shoot apical meristem (SAM), in leaf and flower primordia, in unfertilized ovules and in developing embryos, but not in mature organs) .

The invention also relates to methods for screening for loss of function mutants of MINIYO and/or RTRl in plants. These methods comprise generating a mutant population by using mutagens known in the art. Specifically included are modifications of the endogenous locus by mutagenesis, including chemical mutagenesis, leading to a deletion, insertion or substitution in the endogenous locus. The mutagen may be fast neutron irradiation or a chemical mutagen, for example selected from the following non-limiting list: ethyl methanesulfonate (EMS), methylmethane sulfonate (MMS) , N- ethyl-N-nitrosurea (ENU) , triethylmelamine (l'EM), N-methyl-N- nitrosourea (MNU) , procarbazine, chlorambucil, cyclophosphamide, diethyl sulfate, acrylamide monomer, melphalan, nitrogen mustard, vincristine, dimethylnitosamine, N-methyl- ' -nitro-Nitrosoguanidine (MNNG) , nitrosoguanidine, 2-aminopurine, 7,12 dimethyl-benz (a) anthracene (DMBA) , ethylene oxide, hexamethylphosphoramide, bisulfan, diepoxyalkanes (diepoxyoctane (DEO) , diepoxybutane (BEB) , and the like), 2-methoxy-6-chloro-9 [3-(ethyl-2- chloroethyl ) aminopropylamino ] acridine dihydrochloride (ICR- 170) or formaldehyde.

In one embodiment, the method used to create and analyse mutations is targeting induced local lesions in genomes (TLLING) .

A skilled person will know that different approaches can be used to generate such mutants. In one embodiment, insertional mutagenesis is used. In this embodiment, as discussed in the examples, T-DNA may used as an insertional mutagen which disrupts MINIYO or RTR1 gene expression. These plants thus do not carry a transgene to alter expression of the endogenous locus, but the endogenous locus is modified by mutagenesis. The methods also involve analyzing cell proliferation/differentiation compared to control wild type plants. If cell proliferation/differentiation is delayed, then this may be due to a mutation in MINIYO and/or RTRl .

In one embodiment, methods that solely rely on essentially biologically processes are specifically disclaimed.

Through the description and the claims the word "comprises" and its variants is not intended to exclude other technical features, additives, components or steps. To those skilled in the art other objects, advantages and characteristics of the invention will be apparent partly from the description and partly from the practice of the invention. The following figures and examples are provided by way of illustration, and are not intended to restrict the invention.

The disclosure of all references cited is incorporated. DESCRIPTION OF THE FIGURES

Figure 1. The mutant iyo-1 has delayed differentiation in the shoot (A) and root (B) apical meristems, in the procambium (C) and in the protoderm (D) . (E) The expression of stem cell markers in iyo-1 plants extends beyond its normal meristematic niche. The boxes show the pattern of expression of the markers in wild plants (Wt) . iyo-1 plants develop ectopic shoot apical meristems (F) , multiple flowers from a single bud (G) , ectopic root apical meristems (H) and additional stomas (I) . (J) iyo- l/iyo-2 plants develop twin (double) embryos. (K) The double embryos are viable and germinate, developing into plants with a very low degree of differentiation. (L) iyo-1 plants also occasionally develop double embryos which develop normally. Figure 2. The iyo-1 mutant has a larger number of lateral roots, which develop ectopically in positions in which they do not appear in wild type plants (Wt) : two lateral roots developing opposite one another or even emerging from the same point .

Figure 3. (A) Diagram of the positional map of the mutant iyo- 1. The number of recombinant chromosomes in a total of 1500 genotyped mutant plants is indicated. (B) Alignment of the MINIYO sequence and its orthologues in plants. At: Arabidopsis thaliana; Mt : Meo!icago truncatula; Vv: Vitis vinifera; Os : Oryza sativa; Pp : Physcomitrella patens. The G/E mutation of the iyo-1 allele in the motif united to RNA RGG and conserved glycines is indicated. (C) The hypomorphic allele iyo-1 does not affect accumulation of the IYO transcript. (D) Phenotype of the null allele iyo-2. (E) Phenotype of iyo-l/iyo-2 and iyo- l/iyo-3 embryos. (F) Phenotype of iyo-l/iyo-2 plants. Figure 4. Expression of the β-glucuronidase (GUS) gene (A) and an IYO-GFP fusion (B) under the control of the IYO promoter in roots. (C) Detail of a root epidermis showing nuclear accumulation of IYO-GFP in cells about to begin differentiation. (D-F) Expression in shoot and root apices of IYO-GFP and RPB10-GFP (RPB-GFP) fusions under the control of the 35S promoter. Arrowheads mark nuclear accumulation of IYO-GFP in cells about to begin differentiation at the transition zone of the root. Figure 5. (A) Northern-blot with a specific IYO probe hybridised against samples of total RNA from different tissues and organs. Hypoc+SAM: Hypocotyl and shoot apical meristem of 7-day plants. Cotyledons: cotyledons of 7-day plants. Rosette leaves, cauline leaves, stems, inflorescence apices and flowers were from 30-day plants. (B) In situ hybridisation of inflorescence apices of 22-day plants with an antisense IYO probe. The box shows hybridisation with an IYO sense probe. (C-E) Pattern of expression of the β-glucuronidase (GUS) gene under the control of the IYO promoter. (F) Complementation of the iyo-1 mutant phenotypes with the 35S:: IYO-GFP construct. (G-H) Pattern of expression and subcellular accumulation of IYO-GFP under the control of the 35S promoter. (I) Pattern of expression and subcellular accumulation of GFP-IYO under the control of the 35S promoter. (J) Pattern of subcellular accumulation of GFP-IYO under the control of the IYO promoter in root apices of plants treated with 0.9 μΜ leptomycin B (+LMB) or with an equivalent quantity of the solvent used (- LMB) for 1 or 24 hours. Figure 6. (A) The majority of the 380 genes most significantly induced (p<0.00015957) in the inflorescence apices of wild type plants relative to those of iyo-1 plants (Wt/iyo-1) are over- expressed in inflorescence apices of 35S:: IYO-GFP plants relative to those of wild-type plants ( IYO-GFPoe/Wt ) . (B) Histological sections of the apices of wild-type (Wt) and IYO- GFP over-expressing plants (IYO-GFPoe) 14 and 21 days after sowing. The arrowheads indicate prematurely differentiated cells. (C) Compaction of inflorescence in plants which over- express IYO-GFP (IYO-GFPoe) .

Figure 7. (A) Termination of the primary shoot apical meristem in plants which over-express IYO-HA under the 35S promoter ( IYO-HAoe) . (B) Termination of the primary root apical meristem in plants over-expressing IYO-HA under the 35S promoter (IYO-HAoe) . The boxes show the meristem of wild type plants (Wt) at equivalent stages. (C) Premature differentiation of xylem vessels in lateral root primordia (arrows) and root hairs in epidermal cells prior to their elongation (asterisks).

Figure 8. (A) IYO interacts in vitro with the Rpb3 sub-unit from RNA Polymerase II as shown by the specific pull-down of Rpb3 together with IYO- (B) IYO interacts in vivo with the Rpb3 and RpblO sub-units from RNA Polymerase II as shown by bimolecular reconstitution of YFP in the nucleus. (C) IYO is necessary for the activity of RNA Polymerase II in differentiating organs. Left-hand panel: Levels of the Rpbl sub-unit phosphorylated in Serine 2 of the CTD (Ser2P) in leaf primordia (LP) and in mature leaves (ML) from wild-type (Wt) and iyo-1 mutant plants (iyo) . Right-hand panel: Levels of the mRNA of RPBl in leaf primordia (LP) or mature leaves (ML) from wild-type (Wt) and iyo-1 mutant plants (iyo) (D) Analysis of the relative expression in flowers versus undifferentiated tissues (calluses or cell cultures) of the 380 genes most significantly induced (p<0.00015957) and the 380 most significantly repressed (p<0.00066388 ) in floral meristems (and associated floral primordia) from wild-type plants relative to those from iyo-1 plants (Wt/iyo). (E) Constitutive ubiquitination of Rpbl in iyo-1 plants. Extracts (Inputs) from wild (W) or iyo-1 (i) plants treated ( + ) or not (-) with MG132 were immunoprecipitated (IP) with antibodies against Rpbl and analysed by Western blot with antibodies against Rpbl or against ubiquitin (Ubq) . (F) The over-expression of IYO increases resistance to the transcriptional elongation inhibitor 6-azauracil. Plants grown for 11 days in the presence of increasing concentrations of 6-azauracil (in μΜ) are shown. (G) IYO interacts in vitro with the histone acetyl transferase EL03. (H) IYO interacts genetically with components of the Elongator complex to activate cell differentiation.

Figure 9. Development of atrtrl-1 (rtrl-1) embryos compared to wild type embryos (Wt) at the corresponding stage in the panels above. Figure 10. (A) Formation of ectopic shoot apical meristems in atrtrl-2 plants causes fasciation and thickening of the stem. (B) Ectopic floral meristems give rise to duplicated flowers (and fruits) in atrtrl-2 plants. (C) Duplicated root apical meristems in atrtrl-2 plants. (D) Genetic interaction between AtRTRl and IYO. The double iyo-latrtrl-2 mutants grow as an undifferentiated callus. (E) Expression of the UidA (GUS) gene under the control of the AtRTRl promoter in apical root meristems, lateral root primordia (arrow) and pericycle. (F) The fusion protein AtRTRl-GFP is excluded from the nuclei in undifferentiated cells of the meristem (arrows) .

Figure 11. (A) atrtl-2 plants (rtrl-2) develop ectopic meristemoids which give rise to clusters of stomas (arrowheads) . (B) Cotyledons from iyo-1 and atrtrl-2 plants maintain cells which express the stem cell marker pTMM::TMM- GFP (arrowheads) at later stages than cotyledons from wild type plants (Wt).

Figure 12. (A) The AtRTRl-GFP protein is excluded from the nucleus in untreated plants (arrowheads) . (B) Treatments with leptomycin B, an inhibitor of Exportinl, causes nuclear accumulation of AtRTRl-GFP (arrows). Figure 13. IYO interacts in vivo with the AtRTRl as shown by bimolecular reconstitution of YFP in the nucleus in two different combinations of fusions of AtRTRl and IYO with nYFP and cYFP.

Figure 14. AtRTRl-YFP accumulates in the nucleus when co- expressed with IYO-HA (AtRTRl-YFP+1YO-HA) but not when expressed on its own (AtRTRl-YFP) . Figure 15. The atrtrl-2 and iyo-1 mutants have almost identical changes in the transcriptome relative to wild type plants. The majority of the 380 genes most significantly induced (p<0.00015957) or repressed genes (p<0.00066388 ) in the inflorescence apices of wild-type plants relative to those of iyo-1 plants (Wt /iyo-1) are similarly affected (induced or repressed respectively) in inflorescence apices of wild type plants relative to those of atrtrl-2 plants (Wt/art-2) .

Figure 16. Alignment of protein sequences coded by orthologous genes of MINIYO in a representative set of plants using the Clustal W program. The ordered sequences, from top to bottom, are those of: Arabidopsis thaliana, Arabidopsis lyrata, Brachypodium distachyon, Citrus Clementina, Citrus sinensis, Manihot sculenta, Oryza sativa, Populus trichocarpa, Prunus persica, Ricinus communis, Setaria italica, Sorghum bicolor, Vitis vinifera, Zea mays, Physcomitrella patens, Carica papaya, Glycine max, Medicago truncatula and Eucalyptus grandis . Figure 17. Phylogenetic tree constructed from the alignment of the polypeptide sequence of the orthologues of MINIYO using the Clustal W programme.

Figure 18. Examples of highly-conserved domains in the MINIYO proteins of plants. The sequences, in order from top to bottom, are those of: Arabidopsis thaliana, Arabidopsis lyrata, Brachypodium distachyon, Citrus Clementina, Citrus sinensis, Manihot sculenta, Oryza sativa, Populus trichocarpa, Prunus persica, Ricinus communis, Setaria italica, Sorghum bicolor, Vitis vinifera, Zea mays, Carica papaya, Glycine max, Meo!icago truncatula, Eucalyptus grano!is and Physcomitrella patens. The amino acids of the MINIYO protein of Arabio!opsis thaliana corresponding to the domains shown are: (a) aa. 960- 980. This domain contains the RGG motif mutated into the hypomorphic iyo-1 allele of Arabidopsis which is conserved in all the plant orthologues ; (b) aa. 209-255; (c) aa. 317-396;

(d) aa. 350-389.; (e) aa. 417-437; (f) aa. 529-559; (g) aa. 529-597; (h) aa. 1136-1145; (i) aa. 1144-1416.

Figure 19. Alignment of protein sequences coded by orthologous genes of AtRTRl in a representative set of plants using the Clustal W programme. The sequences in order from top to bottom are those of: Arabidopsis thaliana, Carica papaya, Cucumis sativa, Eucalyptus grandis, Glycine max, Mimulus guttatus, Manihot esculenta, Populus trichocarpa, Prunus persica, Ricinus communis, Vitis vinifera, Zea mays, Sorghum bicolor, Setaria italica, Oryza sativa, Brachypodium distachyon and Picea glauca.

Figure 20. Phylogenetic tree constructed from the alignment of the polypeptide sequences of the orthologues of AtRTRl using the Clustal W programme.

Figure 21. Examples of highly-conserved domains in the RTR1 proteins of plants. The sequences, in order from top to bottom, are those of: Arabidopsis thaliana, Carica papaya, Cucumis sativa, Eucalyptus grandis, Glycine max, Mimulus guttatus, Manihot esculenta, Populus trichocarpa, Prunus persica, Ricinus communis, Vitis vinifera, Zea mays, Sorghum bicolor, Setaria italica, Oryza sativa, Brachypodium distachyon and Picea glauca. The amino acids of the AtRTRl protein of Arabidopsis thaliana corresponding to the domains shown are: (a) aa. 39-61. This domain includes catalytic cysteine C56 which is strictly conserved in all the orthologues; (b) aa. 39-61; (be) aa. 77-89; (d) aa. 429-435;

(e) aa. 473-507; (f) 552-589. Figure 22. Seed yield test of a line co-suppressed in AtRTRl . Seed yield was measured in wild type Arabidopsis plants (Col-0 plants) and in plants from a 35S : :AtRTRl-GFP line displaying co-supression of the AtRTRl-GFP transgene and of the endogenous AtRTRl gene (si-art plants) . Six independent experiments were carried out. The plants were germinated in sterile MS media supplemented with 1% sucrose and transplanted to soil in individual pots after 1 week (10-16 plants per genotype in each experiment) . Seeds were collected from individual plants after they were fully dried and the total seed weight measured. For comparing the results of the different experiments, we calculated the relative yield of each plant as the ratio of the yield of that plant relative to the average yield of control plants (Col-0) in that particular experiment. (A) Average relative seed yield of Col-0 and si- art plants in all six experiments combined. A 12% increase in the average seed yield of si-art plants is observed, with a p- value of 0,006 in an unpaired two tailed t-test. (B) Average relative seed yield of Col-0 and si-art plants in each of the six independent experiments. In experiments 3 and 6 the yield of si-art plants is increased 32% and 27% over that of the control plants (p-value=0 , 006 ) . The error bars represent standard deviation. Figure 23. Phenotype of 35S::IYO-GFP tomato plants. Shown are untransformed tomato plants of the variety Moneymaker (TMM) and three independent transgenic plants of the same variety expressing a 35S: : IYO-GFP construct (Lines 1-3) . Line 1 displays determinate growth of the primary shoot. The arrow marks the terminated primary shoot. Lines 2 and 3 display reduced apical dominance resulting in a shorter stature and increased branching. Arrowheads mark premature outgrowth of lateral buds. REFERENCES

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EXAMPLES

The following specific examples provided in this patent document serve to illustrate the nature of this invention.

These examples are included purely for illustrative purposes and should not be interpreted as limiting the invention claimed here. Therefore the examples described below illustrate the invention without limiting the scope of its application . EXAMPLE 1

1. Identification of the miniyo-1 (iyo-1) mutant. The iyo-1 mutant is identified in a population mutagenised by ethylmethane sulphonate in the Landsberg erecta ecotype which brought about a change of amino acid (G962E) in the coded protein .

2. Positional map of the iyo-1 mutant to provide evidence of point mutations in the IYO gene. The mutant was crossed with accession Col-0 and it was proved that the iyo-1 phenotype is inherited in a recessive way. F2 plants with a mutant phenotype were used to clone the mutation through positional mapping. The analysis of more than 1500 mutant plants made it possible to establish the position of the mutation to 6 genes in chromosome 4. Sequencing of the 6 genes showed that there was a single mutation in the At4g38440 gene in iyo-1 mutants. This was a point mutation (G to A) .

3. Generation of ectopic stem cells in an iyo-1 mutant. It was proved by microscope studies and by analysing the expression of markers that one of the phenotypes of the iyo-1 mutant was the formation of ectopic stem cells in all meristems of the plant .

4. Total blocking of IYO activity in iyo-2 and iyo-3 mutants. Mutants were obtained that had a T-DNA insertion in the At4g38440 gene and it was proved that they cause blocking of endosperm development and early arrest of embryogenesis . iyo-2 has T-DNA insertion at nucleic acid position 234 (Salk 099873) . iyo-2 has T-DNA insertion at nucleic acid position 1357 (Salk 0692_gl2) .

5. Combination of the hypomorphic allele iyo-1 with the null alleles {iyo-2 or iyo-3) . The allele combination iyo-1 / iyo-2 or iyo-1/ iyo-3 caused almost total blocking of differentiation of the embryo and the formation of ectopic embryos from the suspensor. The embryos were viable and after germination the plants grew as a callus-like structure with multiple meristematic poles and producing only rudimentary leaves.

6. Double embryos in an iyo-1 mutant. Although with low penetrance, we observed that the iyo-1 mutant can also form double embryos from the suspensor, which apparently developed normally .

7. Transcriptional and post-transcriptional regulation of the expression of IYO .

7.1. Monitoring of activity of the IYO promoter.

Through a Northern type analysis, in situ hybridisation and studies of the promoter we have demonstrated that the IYO gene is expressed specifically during embryogenesis in meristem cells and in cells adjacent to the meristem which are initiating differentiation.

7.2. Nuclear accumulation of IYO protein

Confocal microscopic studies of functional fusions of IYO protein with GFP which complement the iyo-1 and iyo-2 mutants have shown that IYO is excluded from the nucleus in undifferentiated cells in a manner which is dependent on Exportinl, while it accumulates in the nucleus in cells which are initiating differentiation.

8. Over-expression of IYO or its fusions with proteins or peptides such as GFP, HA, FLAG under the control of the 35S promoter .

Col-0 Arabidopsis plants were transformed with constructs which expressed fusions of the epitopes GFP, 3XHA or FLAG at the C-terminal of IYO under the control of the 35S promoter. The lines which accumulated larger quantities of the transgene transcript and the transgenic protein had gain of function phenotypes, from premature differentiation in the shoot apical meristem and compaction of inflorescence but no apparent effect on the root meristem to termination of the shoot and root apical meristems in lines with the maximum levels of accumulation .

9. Physical interactions between IYO protein and RNA Polymerase II (Pol II) and with elongation complexes. Through pull-down studies with proteins synthesised in bacteria and in vitro, studies of bimolecular complementation of YFP, measurements of accumulation of different phosphorylated and ubiquitinised forms of the RPB1 sub-unit and analysis of genetic interactions we have proved that IYO interacts with Pol II and with the elongator complex and is required for maintaining the global levels of elongating Pol II in differentiating tissues. EXAMPLE 2

1. Identification of the gene At5g26760 (atrtrl) . Through the analysis of co-expression we discovered the At5g26760 gene which is highly co-expressed with IYO and codes for a protein homologous to RTR1, a yeast protein which functions as a transition phosphatase that dephosphorylates Ser5 in the CTD from the RPB1 sub-unit of Pol II to promote the shift from initiation to productive elongation.

2. Analysis of AtRTRl function in the mutant alleles atrtrl-1 (SALK_012339, T-DNA insertion at nucleic between nucleic acid

414 and 415) and atrtrl-2 (SALK_115762, T-DNA insertion at nucleic between nucleic acid 864 and 865) . We obtained homozygous mutants of atrtrl-1 , showing by Nomarski microscopy that it caused blocking of differentiation in the embryos, the formation of ectopic embryos from the suspensor and early embryo arrest. The homozygous mutant atrtrl-2 has phenotypes very similar to the iyo-1 mutant: enlarged shoot apical meristems, thicker stems, formation of ectopic shoot, floral and root meristems, delayed differentiation of the protodermis and the formation of clusters of stomas.

3. Generation of ectopic stem cells in atrtrl-2 mutants. Microscopic studies and analysis of marker expression reveal that ectopic stem cells form in all meristems in the atrtrl-2 mutants .

4. Investigation of gene interaction between IYO and AtRTRl . The double mutant iyo-latrtrl-2 was obtained and it was shown that cell differentiation was completely blocked, the plants growing as calluses of undifferentiated cells, demonstrating clear gene interaction.

5. Investigation into the over-expression of IYO in an atrtrl- 2 mutant context. Heterozygous plants from IYO-3XHA over- expressing lines displaying termination of shoot and root meristems were crossed with homozygous atrtrl-2 plants. In the F2, homozygous plants for the IYO-3XHA construct were recovered that were homozygous for atrtrl-2 or were wild type for the AtRTRl locus. It was proved that while IYO-3XHA over- expression in wild type plants produced shoot and root meristem termination, in the atrtrl-2 background it did not cause any phenotype, demonstrating that AtRTRl activity is required for IYO function.

6. Investigation into the expression of AtRTRl in transgenic plants which express an AtRTRl promoter construct and the first three exons and introns of AtRTRl translat ionally fused to the UidA (GUS) gene. Histological studies of GUS activity in transgenic plants expressing the UidA gene under the control of the AtRTRl promoter show that this is specifically located in embryos, meristem cells and cells adjacent to the meristem which are beginning to differentiate.

7. Investigation into the accumulation of RTR1 fused to GFP under the control of the constitutive 35S promoter and the AtRTRl promoter. Confocal microscopy studies of plants expressing stable functional fusions of AtRTRl protein to GFP which complement atrtrl-1 mutants have demonstrated that AtRTRl is excluded from the nucleus in undifferentiated cells in a form dependent on Exportinl. Example 3 Bioinformatics analysis

To search for candidate nuclear localization signals (NLS), the Arabidopsis IYO and AtRTRl protein sequences were submitted to the cNLS mapper server (http://n_.s- mapper.iab.keio.ac.jp). This tool searches for classical NLS (cNLS) recognized by the nuclear receptor importin a . cNLSs detected with this tool have been validated in a number of yeast proteins (Kosugi et al . , PNAS 2009) . The server predicted in IYO a monopartite NLS (aa. 250-262) and a bipartite NLS (aa. 1397-1420), both with a score of 10, the maximum possible. When a GUS-GFP reporter protein was fused with NLSs having a score between 8-10 they accumulated in the nucleus (Kosugi et al . , PNAS 2009, JBC 2009). In the case of AtRTRl, the server predicted a bipartite NLS with a long linker and a score of 5.2 in the middle of the protein (aa. 340-368) . GUS-GFP proteins fused with NLSs with a score 3-7 were localized in the cytosol and the nucleus (Kosugi et al . , PNAS 2009, JBC 2009) . Moreover, when bi-partite NLSs have long linkers they are functional normally in unstructured regions, which frequently coincide with the N- and C-terminal ends of the proteins. Thus, for IYO, two high confidence cNLSs were predicted, while for AtRTRl, no clear cNLSs were detected. It is possible that AtRTRl is imported through an importin - independent pathway, as is the case for the majority of nuclear proteins. In this regard, we have shown that nuclear IYO leads to AtRTRl accumulation in the nucleus, which could be by mediating its import. To search for candidate nuclear export signals (NES), the Arabidopsis IYO and AtRTRl protein sequences were submitted to the NetNES server (http://www.cbs.dtu.dk/services/NetNES). This tool searches for leucine-rich NES, and predictions have been validated (for example for BRCA1, Thompson et al . , JBC 2005) . The server predicted a NES in IYO (aa. 432-440) and in AtRTRl (aa 340-349). Consistent with these predictions, inhibition of the NES receptor CRM1 with leptomycin B, leads to nuclear accumulation of IYO and AtRTRl in Arabidopsis and Nicotiana cells, suggesting that their nuclear export is NES- dependent. Moreover the truncated C-terminal half of AtRTRl (aa 305-735) that contains the predicted NES is exported from the nucleus . To test for altered localization, mutated versions of the proteins are fused to GFP and their subcellular distribution by transient expression in Nicotiana benthamiana leaves is analysed (where wild type IYO accumulates primarily in the nucleus and AtRTRl in the cytosol) . Analysis is also carried out in in Arabidopsis cell cultures untreated (where both proteins are localized in the cytosol) or treated with leptomycin B (where both proteins are localized in the nucleus) . In the case of IYO constructs are designed lacking each predicted NLSs and one combining mutations in both NLSs, as it has been shown in other proteins with multiple NLSs that only after mutating all of them is their nuclear import blocked (i.e. Zhang et al . , PNAS 2000; Yeung et al . , J. Cell Biochem. 2008) . Homology Analysis

Alignment by clustalW of the whole polypeptide sequence shows that the % identity between IYO orthologues from embryophytes (A thaliana, A lyrata, Brachypodium, Carica , citrus, Eucalyptus, Manihot, Medicago, Oryza, Physcomitrella, Populus, Prunus, Ricinus, Selaginella, Sorghum, Vitis, Zea) is higher than 30%. If only angiosperm sequences are aligned the overall identity is higher than 39%.

Alignment by clustalW of the whole polypeptide sequence shows that the % identity between IYO orthologues from embryophytes (A thaliana, A lyrata, Brachypodium, Carica, citrus, Eucalyptus, Manihot, Medicago, Oryza, Physcomitrella, Populus, Prunus, Ricinus, Picea, Sorghum, Vitis, Zea) is higher than 25%. If only spermatophyte sequences are aligned the overall identity is higher than 32%.

An Interpro scan of the polypeptide sequence of IYO reveals two conserved domains IPR013929 (PF08620) and IPR013930 (PF08621) in the N-terminus of the protein (aa 209-255 and 317-396, respectively), which are found in orthologues from plants, animals and fungi. Moreover, blast searches reveal two other domains highly conserved in IYO orthologues from multicellular eukaryotes (aa 529-597 and 1144-1416) . In addition, IYO has a glycine rich domain with an RGG motif (aa 960-980) that is strictly conserved in orthologues from plants. Glycine rich domains and RGG boxes have been linked to nucleic acid binding (Gendra et al . , Plant Journal 2004) . Moreover, the iyo-1 allele is a missense mutation that changes the motif from RGG to RGE and reduces the transcriptional activity of the protein. This indicates that this domain contacts the DNA or the nascent transcript to facilitate transcription. This domain is not clearly identifiable in the animal orthologues of IYO, but alignment of their sequences reveals a high number of conserved glycines in this region.

AtRTRl contains a conserved domain (DUF408) with a zinc-finger like motif located at the N-terminus of the protein that is found in all the orthologues from plants, animals and fungi. A consensus sequence for that motif derived from sequences from multicellular eukaryotes is (in bold the putative Zinc- coordinating cysteines) : D [ IV] V [ TDEV] ER [ASTF ] I [AVI S ] [KND] [LAV]CGY[TP] [ LRA] CXXXLX ₇ _

is [YF] [RK]IS[LT] [KSR] [TAED] [HKN] [KR] VYD [ IL ] [ THEQ ] EXXX [FY] CXXXC

A blast search against the non-redundant protein sequence database at NCBI with the corresponding sequence from Arabidopsis

DVVTERAIAKLCGYTLCQRFLPSDVSRRGKYRI SLKDHKVYDLQETSKFCSAGC

retrieved the AtRTRl orthologues from plants and animals and fungi with a low E-value (< 10 ^~6 ) .

The zinc-finger-like-motif has been implicated in interaction with the RNA Polymerase II C-terminal domain (CTD) and the Integrator complex in humans and is required for CTD- phosphatase activity in yeast and humans (Mosley et al . , 2009; Egloff et al . , 2011) . Interestingly, this motif is also required for interaction of AtRTRl with IYO. Substituting for alanine the putative zinc coordinating cysteine residues (C56A/C61A or C94A/C98A) in the full-length AtRTRl protein abrogates interaction with IYO. Intriguingly, however, both the truncated N-terminal and the C-terminal halves of AtRTRl can interact with IYO, suggesting that although AtRTRl binds at both ends of the protein to IYO, it requires an intact zinc-finger-like motif in the context of the full length protein. EXAMPLE 4

We analyzed the expression pattern of an AtRTRl promoter construct driving the GUS reporter gene (pART: : GUS) . This same promoter driving an AtRTRl cDNA fully complements atrtrl mutant phenotypes, indicating that it reproduces the activity of the endogenous gene. In roots, pART: : GUS was strongly expressed in root apical meristem (RAM) and in transition cells, in the pericycle layer and in lateral root primordia. In the aerial part of the plant, pAtRTRl : : GUS was expressed in the shoot apical meristem (SAM), in leaf and flower primordia, in unfertilized ovules and in developing embryos, but not in mature organs. These results suggest that AtRTRl is exclusively expressed at sites of active cell proliferation and differentiation, in a pattern highly similar to that of IYO.

To determine the subcellular distribution of AtRTRl we analyzed a translational fusion to GFP . Under the control of the constitutive 35S promoter ( 35S : :AtRTRl-GFP) we only obtained transgenic lines expressing low levels of the tagged protein that complemented partially the atrtrl-1 null mutation (i.e: atrtrl-1 plants transgenic for this construct were viable but resembled the hypomorphic atrtrl-2 plants) . These results suggest that expressing high levels of AtRTRl protein in a constitutive manner may be deleterious for plant development. We then transformed plants with AtRTRl-GFP driven by its own promoter (pAtRTRl ::AtRTRl-GFP) . The resulting lines had higher levels of expression and complemented fully the atrtrl-1 null mutation. This indicates that pAtRTRl ::AtRTRl- GFP reproduces the activity of the endogenous gene and can be used as a proxy for localization of ART. pAtRTRl ::AtRTRl-GFP fluorescence in the root was restricted to the tip, consistent with the pattern of expression found in pAtRTRl-GUS lines. Importantly, the fluorescence was found in the cytosol and strongly excluded from the nucleus (Figure 6A-B) . Similarly, in Nicotiana benthamiana leaf cells transiently expressing a 35S: :ATRTRl-GFP construct, fluorescence was confined to the cytosol. In yeast and mammalian cells, the orthologues of ATRTR1, RTR1 and RPAP2, are also localized primarily in the cytosol, but they redistribute partially to the nucleus upon inhibition of the XP01 nuclear export receptor with leptomycin B (LMB) , which also inhibits the Arabidopsis receptor (Kudo et al . , 1999, Haasen et al . , 1999). After treating Arabidopsis with LMB, nuclear accumulation of ATRTRl-GFP was observed in cells of the root transition zone and in Nicotiana benthamiana leaf epidermal cells. These results suggest that, at least in differentiating and mature cells, AtRTRl is imported into the nucleus, although the higher rate of nuclear export leads to its steady state accumulation in the cytosol. The remarkable conservation in nuclear-cytoplasmic shuttling of RTR1 homologues in all eukaryotic lineages indicates that it constitutes an important regulatory mechanism for this family of phosphatases.

We tested for the in vivo interaction between IYO and AtRTRl through a bimolecular fluorescence complementation assay in epidermal cells from Nicotiana benthamiana leaves. YFP complementation was observed with different combinations of split YFP fused at the N- or C-terminus of the respective proteins and not in any of the multiple negative controls tested. Interestingly, the reconstituted fluorescence was localized in the nucleus, suggesting that these proteins interact specifically in this compartment, possibly to regulate transcription. Moreover, we found that both the DUF408-containing N-terminal half and the C-terminal half of AtRTRl interact with IYO, suggesting that the two proteins bind through at least two sites. Unexpectedly, substituting the putative zinc coordinating cysteine residues for alanines (C56A/C61A or C94A/C98A) in the full-length AtRTRl protein abrogates the interaction with IYO, suggesting that although AtRTRl binds at both ends of the protein to IYO, it requires an intact zinc-finger-like motif for binding in the context of the full length protein.

Considering that AtRTRl-GFP expressed in Nicotiana benthamiana cells is found exclusively in the cytosol, it was surprising to find AtRTRl strongly interacting with IYO in the nucleus. We reasoned that when bound to IYO, AtRTRl is retained in the nucleus. To test this we expressed AtRTRl-GFP together with IYO-HA or an empty vector. Importantly, co-expression with IYO-HA led to nuclear AtRTRl-GFP accumulation in Nicotiana cells, confirming that IYO retains AtRTRl in the nucleus. The levels of nuclear fluorescence were much lower than in the split YFP assays, where the IYO-AtRTRl complex is stabilized through the irreversible reconstitution of YFP. This suggest that the IYO-AtRTRl association is very transient, explaining why nuclear AtRTRl accumulation cannot detected in transition cells of the meristem, even though IYO is present in the nucleus of those cells. To test for genetic interaction between IYO and ATRTRl , we combined the atrtrl-2 with the iyo-1 hypomorphic mutations. Differentiation in the iyo-latrtl-2 double mutants was almost completely blocked and the plants eventually developed as a friable callus of undifferentiated cells. This phenotype is much stronger than the sum of the phenotypes of the single mutants, and indicates a strong genetic interaction of IYO and AtRTRl in the control of cell differentiation, supporting a close functional interaction. Transcriptome analysis of iyo-1 mutants supports that IYO functions as a global transcriptional regulator of developmental programs. In inflorescence meristems, IYO was required for proper expression of flower development programs, including activating the expression of the homeotic flower organ identity genes, which are the master regulators of organogenesis in those meristems. We performed a similar analysis in the atrtrl-2 mutant and we found a very high overlap (>80%) in the up-regulated and down-regulated genes in iyo-1 and atrtrl-2 inflorescences meristems relative to wild type. These results indicate that IYO and AtRTRl regulate as a complex transcription of developmental programs. Consistent with their functioning together, we found that a functional AtRTRl gene is required for IYO activity in cell differentiation. Over expression of IYO-HA provokes premature differentiation and termination of the root and shoot apical meristems. Importantly, in an atrtrl-2 background or in AtRTRl co-suppressed line, these effects of IYO-HA over expression are eliminated, demonstrating that IYO requires AtRTRl for its activity .

EXAMPLE 5 YIELD ANALYSIS IN ARABIDOPSIS We have measured seed yield in a line co-suppressed in AtRTRl, which was chosen because it had a weak loss of function phenotype. This line was characterized by a few extra shoot meristems, but otherwise normal development. Seed yield test

During the generation of lines transgenic for a 35S: :AtRTRl - GFP construct, we isolated a line (si-art line) showing co- suppression of the transgene and of the endogenous AtRTRl gene. The phenotype of si-art plants is weaker than that of the hypomorphic atrtrl-2 allele, forming some ectopic shoot apical meristems (SAMs) that give rise to split primary shoots but otherwise developing very similarly to wild type plants. To test if the formation of ectopic SAMs affects yield, we measured seed production in si-art plants and in the corresponding wild type background (Col-0) . We carried out six independent experiments (experiments 1-3 in the greenhouse, 4- 6 in a growth chamber) and harvested seeds after the plants were fully dried. In each experiment, we measured the seed yield (in weight) of individual plants, and then calculated their yield relative to the average yield of control plants (Col-0) in that particular experiment. Combining in this way the data from all six experiments, we found a 12% increase in the average seed yield of si-art plants, with a p-value of 0, 006 in an unpaired two tailed t-test. The results are shown in Figure 22. If the individual experiments are analyzed separately, we find significant differences (p-value<0 , 05 ) between the average yields in experiments 3 and 6, in which the yield of si-art plants is increased 32% and 27%, respectively over that of the control plants (p-value=0 , 006 ) .

EXAMPLE 6 EXPERIMENTS IN TOMATO

Tomato plants of the cultivar Moneymaker were transformed by co-cultivation with Agrobacterium tumefaciens with a sequence coding for the Arabidopsis IYO protein fused to GFP under the control of the 35S promoter. This construct fully complements the phenotypes of weak (iyo-1) and null (iyo-2) alleles in Arabidopsis. Plants were regenerated from independent transformed calli and transplanted to soil. We analyzed roots from those lines in the confocal microscope and observed accumulation of GFP fluorescence in nuclei of differentiated cells, demonstrating that they are transgenic for the construct and that subcellular localization of the IYO protein in tomato is the same as in Arabidopsis. The development of the transgenic lines reveals that the Arabidopsis protein is functional in tomato and that its overexpression provokes premature onset of cell differentiation as it does in Arabidopsis. Some of the transgenic lines (e.g. Line 1, Fig 23) show a determinate growth pattern, in contrast to untransformed Moneymaker plants that are indeterminate (Figure 23) . In other lines (e.g. Lines 2 and 3, Fig 23) the branching pattern is altered (Figure 23) . The transgenic lines are fertile and produces fruits with viable seeds.

Sequence listing

SEQ ID NO:l MINIYO cDNA Arabidopsis thaliana

ATGGAGCAAAGTAGCGGGAGAGTCAATCCGGAACAGCCGAACAACGTCTTGGCGAGC CTTGTCGGGAGCATCGTGGA

GAAAGGAATATCGGAGAATAAGCCTCCAAGCAAGCCGCTTCCCCCAAGGCCCTCCCT TCTTTCCTTCCCCGTCGCTCGT

CATCGTTCTCACGGACCCCATTTGGCTCCTGTGGGAAGCAGCATAGCACAACCTAAG GATTACAATGACGATCAGGAAG AAGAAGAAGCAGAAGAACGTTTCATGAATGCAGACTCCATTGCTGCTTTTGCTAAACCGC TTCAAAGAAAAGAGAAGAAA GACATGGACCTCGGGAGGTGGAAAGATATGGTCTCTGGGGATGATCCTGCATCCACACAT GTCCCTCAGCAATCAAGG AAACTTAAGATCATTGAAACGAGACCGCCCTATGTTGCTTCAGCCGATGCGGCCACTACA TCCAGCAACACTTTACTGG CTGCCAGGGCATCAGACCAGAGAGAGTTTGTTTCTGATAAAGCACCGTTTATTAAAAATT TGGGAACCAAGGAAAGGGTT CCTTTAAACGCTTCTCCTCCCCTAGCTGTTTCGAATGGACTTGGGACTCGACACGCGTCT TCGTCTCTTGAAAGTGATAT TGATGTTGAGAACCATGCAAAGTTGCAGACAATGTCACCCGACGAGATTGCTGAGGCTCA GGCTGAGTTATTGGACAAG ATGGATCCTGCACTACTCTCCATTTTGAAGAAACGAGGTGAGGCAAAATTGAAGAAGCGA AAGCATTCTGTGCAGGGGG TTTCCATCACCGATGAAACAGCAAAGAATTCAAGAACTGAGGGTCATTTTGTCACTCCTA AAGTGATGGCAATACCGAAA GAAAAAAGTGTGGTGCAAAAGCCAGGGATAGCCCAAGGATTCGTGTGGGATGCATGGACT GAGAGGGTTGAGGCAGCC AGAGACTTGAGATTTTCTTTTGACGGGAATGTTGTTGAGGAAGATGTTGTCTCGCCAGCT GAAACTGGTGGAAAGTGGT CTGGTGTTGAATCTGCTGCCGAACGTGATTTCTTGAGAACCGAGGGGGATCCTGGGGCCG CAGGTTACACTATCAAAG AAGCTATTGCTCTTGCACGAAGTGTGATTCCCGGGCAGAGATGTCTTGCTTTGCATCTGC TTGCATCTGTACTCGACAAA GCTTTGAACAAACTTTGTCAAAGCAGAATAGGCTACGCAAGGGAAGAAAAAGATAAATCC ACTGACTGGGAAGCCATCT GGGCTTATGCCCTTGGACCGGAACCTGAGCTTGTCTTAGCATTGAGGATGGCTCTTGATG ACAACCATGCCTCTGTTGT TATAGCATGTGTAAAAGTGATTCAGTGTCTACTGAGCTGTTCTCTTAACGAGAATTTCTT TAATATTCTGGAGAACATGGG ACCACACGGGAAAGATATCTTCACGGCCTCGGTGTTCAGGAGTAAGCCGGAAATTGATCT TGGCTTCCTCCGTGGTTGC TACTGGAAGTACAGCGCTAAACCCTCCAATATTGTTGCGTTCCGTGAAGAAATCTTGGAT GACGGGACAGAAGATACGG ATACTATTCAGAAAGATGTTTTTGTAGCCGGACAAGATGTTGCTGCTGGTCTCGTCAGAA TGGATATCCTTCCAAGAATTT ATCACCTTCTGGAGACAGAACCAACAGCAGCGCTTGAGGACAGCATAATCTCTGTTACTA TTGCGATAGCAAGGCATTCT CCAAAATGCACAACTGCAATCTTGAAGTATCCCAAATTTGTGCAAACAATTGTGAAAAGA TTCCAATTGAACAAAAGAATG GACGTTCTTTCTTCTCAGATCAACTCTGTCCGCCTCTTAAAGGTGTTGGCCCGGTATGAT CAAAGTACTTGCATGGAATT TGTGAAGAATGGGACTTTCAATGCGGTCACATGGCATTTGTTTCAGTTCACCTCATCTCT TGACTCATGGGTGAAGCTAG GGAAGCAGAACTGCAAGCTTTCATCTACCTTGATGGTTGAACAGCTCCGGTTTTGGAAGG TCTGTATCCATAGTGGCTG TTGCGTATCTCGCTTCCCAGAGCTATTCCCAGCTCTGTGTCTGTGGTTGAGTTGTCCATC ATTCGAAAAGCTCAGGGAGA AAAATCTCATCAGCGAGTTTACTTCTGTGTCAAACGAGGCCTACCTGGTCCTTGAGGCTT TTGCCGAGACACTTCCTAAT

ATGTACTCACAAAACATTCCACGGAATGAATCTGGGACATGGGACTGGAGCTATGTT AGCCCTATGATTGATTCAGCACT GAGTTGGATAACATTGGCCCCGCAATTACTCAAGTGGGAGAAAGGAATCGAAAGTGTCTC TGTATCAACTACTACTCTGT TGTGGTTGTATTCAGGTGTCATGCGTACAATTTCCAAAGTCCTTGAGAAAATCTCTGCGG AGGGAGAGGAAGAACCTCT ACCATGGCTACCGGAGTTTGTTCCAAAGATTGGCCTTGCCATTATCAAGCACAAGCTTCT TAGTTTTTCTGTTGCAGACG TAAGTAGGTTTGGAAAAGACTCTTCCAGGTGTTCCTCTTTTATGGAGTATTTGTGTTTTC TAAGAGAACGATCTCAAGATG

ACGAACTAGCATTAGCTTCTGTGAATTGTCTTCATGGGTTAACACGGACTATCGTGT CCATCCAAAATCTGATAGAATCT GCTAGATCCAAGATGAAAGCTCCGCATCAGGTAAGTATTTCCACTGGAGATGAATCTGTG CTTGCAAATGGGATACTGG CAGAGTCTCTGGCTGAGCTAACATCTGTGTCGTGCTCTTTTAGAGATTCTGTTTCATCAG AATGGCCCATCGTGCAATCA ATTGAGCTACATAAACGAGGCGGATTGGCCCCCGGCGTTGGACTTGGTTGGGGAGCTAGC GGTGGTGGGTTTTGGTCA ACCAGAGTTCTGTTGGCACAGGCTGGTGCCGGTCTTCTGAGTCTCTTTCTTAACATCTCT CTGAGCGACTCGCAGAATG

ATCAGGGATCTGTTGGCTTTATGGATAAAGTAAACTCCGCTTTAGCTATGTGTTTGA TTGCAGGTCCAAGGGATTATTTAC TCGTGGAAAGAGCCTTTGAATATGTCCTTAGACCGCATGCTTTAGAACACCTGGCCTGCT GTATCAAGTCAAACAAAAAA AACATATCGTTTGAATGGGAATGCAGCGAAGGGGACTATCATCGTATGAGCAGTATGCTT GCTTCTCACTTCAGACATAG ATGGTTACAGCAAAAGGGAAGATCGATAGCCGAGGAAGGGGTCAGTGGGGTAAGGAAGGG CACAGTTGGTCTGGAGA CTATTCATGAGGACGGTGAAATGTCAAATAGTTCAACTCAGGATAAAAAATCAGACTCCT CGACCATAGAGTGGGCTCAC

CAGAGAATGCCCCTACCTCCACACTGGTTTCTCAGCGCCATCTCAGCAGTCCACAGT GGTAAAACCTCAACAGGGCCAC CAGAATCCACAGAGTTGCTTGAAGTTGCAAAAGCTGGAGTTTTCTTTCTTGCAGGACTTG AGTCATCGTCTGGTTTTGGA TCGCTTCCCTCTCCTGTTGTGAGTGTACCGTTGGTTTGGAAGTTTCACGCTTTGTCTACC GTATTGCTTGTTGGAATGGA CATCATCGAAGACAAGAACACTAGGAACTTGTACAATTATCTGCAGGAGCTTTATGGGCA GTTTCTTGATGAAGCGAGAC TAAATCACCGTGACACTGAGCTTCTGAGGTTCAAGTCAGACATTCATGAGAACTACTCTA CTTTTCTGGAGATGGTGGTG GAGCAGTATGCTGCGGTGTCATATGGTGATGTAGTGTATGGCCGGCAGGTCTCGGTTTAC CTGCATCAATGCGTGGAAC ACTCTGTTCGGCTTTCGGCATGGACAGTGCTCTCCAATGCCCGTGTTCTCGAGCTTCTGC CGAGTCTAGACAAGTGCTT GGGAGAAGCGGATGGTTACCTCGAACCTGTTGAGGAAAATGAGGCCGTCCTTGAGGCCTA CCTGAAGTCATGGACTTG TGGGGCATTGGACAGAGCTGCGACGCGTGGATCAGTAGCCTATACGCTGGTTGTGCATCA CTTTTCATCTTTAGTCTTTT GCAACCAAGCCAAGGATAAAGTATCCCTGCGGAATAAGATTGTCAAGACTCTTGTCAGGG ATTTATCAAGAAAGCGGCA

TCGTGAGGGGATGATGTTAGATCTCCTGCGGTATAAGAAAGGGTCTGCGAACGCCAT GGAAGAAGAAGTGATAGCAGC GGAGACAGAGAAAAGAATGGAGGTGTTGAAAGAGGGTTGCGAAGGGAACTCCACCCTCCT CTTGGAACTGGAGAAGCT GAAATCAGCCGCTCTCTGTGGAAGAAGGTGA

SEQ ID NO: 2 nucleic acid sequence mutant iyo-1 Arabidop thaliana ATGGAGCAAAGTAGCGGGAGAGTCAATCCGGAACAGCCGAACAACGTCTTGGCGAGCCTT GTCGGGAG CATCGTGGAGAAAGGAATATCGGAGAATAAGCCTCCAAGCAAGCCGCTTCCCCCAAGGCC CTCCCTTC TTTCCTTCCCCGTCGCTCGTCATCGTTCTCACGGACCCCATTTGGCTCCTGTGGGAAGCA GCATAGCA CAACCTAAGGATTACAATGACGATCAGGAAGAAGAAGAAGCAGAAGAACGTTTCATGAAT GCAGACTC CATTGCTGCTTTTGCTAAACCGCTTCAAAGAAAAGAGAAGAAAGACATGGACCTCGGGAG GTGGAAAG ATATGGTCTCTGGGGATGATCCTGCATCCACACATGTCCCTCAGCAATCAAGGAAACTTA AGATCATT GAAACGAGACCGCCCTATGTTGCTTCAGCCGATGCGGCCACTACATCCAGCAACACTTTA CTGGCTGC CAGGGCATCAGACCAGAGAGAGTTTGTTTCTGATAAAGCACCGTTTATTAAAAATTTGGG AACCAAGG AAAGGGTTCCTTTAAACGCTTCTCCTCCCCTAGCTGTTTCGAATGGACTTGGGACTCGAC ACGCGTCT TCGTCTCTTGAAAGTGATATTGATGTTGAGAACCATGCAAAGTTGCAGACAATGTCACCC GACGAGAT TGCTGAGGCTCAGGCTGAGTTATTGGACAAGATGGATCCTGCACTACTCTCCATTTTGAA GAAACGAG GTGAGGCAAAATTGAAGAAGCGAAAGCATTCTGTGCAGGGGGTTTCCATCACCGATGAAA CAGCAAAG AATTCAAGAACTGAGGGTCATTTTGTCACTCCTAAAGTGATGGCAATACCGAAAGAAAAA AGTGTGGT GCAAAAGCCAGGGATAGCCCAAGGATTCGTGTGGGATGCATGGACTGAGAGGGTTGAGGC AGCCAGAG ACTTGAGATTTTCTTTTGACGGGAATGTTGTTGAGGAAGATGTTGTCTCGCCAGCTGAAA CTGGTGGA AAGTGGTCTGGTGTTGAATCTGCTGCCGAACGTGATTTCTTGAGAACCGAGGGGGATCCT GGGGCCGC AGGTTACACTATCAAAGAAGCTATTGCTCTTGCACGAAGTGTGATTCCCGGGCAGAGATG TCTTGCTT TGCATCTGCTTGCATCTGTACTCGACAAAGCTTTGAACAAACTTTGTCAAAGCAGAATAG GCTACGCA AGGGAAGAAAAAGATAAATCCACTGACTGGGAAGCCATCTGGGCTTATGCCCTTGGACCG GAACCTGA GCTTGTCTTAGCATTGAGGATGGCTCTTGATGACAACCATGCCTCTGTTGTTATAGCATG TGTAAAAG TGATTCAGTGTCTACTGAGCTGTTCTCTTAACGAGAATTTCTTTAATATTCTGGAGAACA TGGGACCA CACGGGAAAGATATCTTCACGGCCTCGGTGTTCAGGAGTAAGCCGGAAATTGATCTTGGC TTCCTCCG TGGTTGCTACTGGAAGTACAGCGCTAAACCCTCCAATATTGTTGCGTTCCGTGAAGAAAT CTTGGATG ACGGGACAGAAGATACGGATACTATTCAGAAAGATGTTTTTGTAGCCGGACAAGATGTTG CTGCTGGT CTCGTCAGAATGGATATCCTTCCAAGAATTTATCACCTTCTGGAGACAGAACCAACAGCA GCGCTTGA

GGACAGCATAATCTCTGTTACTATTGCGATAGCAAGGCATTCTCCAAAATGCACAAC TGCAATCTTGA AGTATCCCAAATTTGTGCAAACAATTGTGAAAAGATTCCAATTGAACAAAAGAATGGACG TTCTTTCT TCTCAGATCAACTCTGTCCGCCTCTTAAAGGTGTTGGCCCGGTATGATCAAAGTACTTGC ATGGAATT TGTGAAGAATGGGACTTTCAATGCGGTCACATGGCATTTGTTTCAGTTCACCTCATCTCT TGACTCAT GGGTGAAGCTAGGGAAGCAGAACTGCAAGCTTTCATCTACCTTGATGGTTGAACAGCTCC GGTTTTGG

AAGGTCTGTATCCATAGTGGCTGTTGCGTATCTCGCTTCCCAGAGCTATTCCCAGCT CTGTGTCTGTG GTTGAGTTGTCCATCATTCGAAAAGCTCAGGGAGAAAAATCTCATCAGCGAGTTTACTTC TGTGTCAA ACGAGGCCTACCTGGTCCTTGAGGCTTTTGCCGAGACACTTCCTAATATGTACTCACAAA ACATTCCA CGGAATGAATCTGGGACATGGGACTGGAGCTATGTTAGCCCTATGATTGATTCAGCACTG AGTTGGAT AACATTGGCCCCGCAATTACTCAAGTGGGAGAAAGGAATCGAAAGTGTCTCTGTATCAAC TACTACTC

TGTTGTGGTTGTATTCAGGTGTCATGCGTACAATTTCCAAAGTCCTTGAGAAAATCT CTGCGGAGGGA GAGGAAGAACCTCTACCATGGCTACCGGAGTTTGTTCCAAAGATTGGCCTTGCCATTATC AAGCACAA GCTTCTTAGTTTTTCTGTTGCAGACGTAAGTAGGTTTGGAAAAGACTCTTCCAGGTGTTC CTCTTTTA TGGAGTATTTGTGTTTTCTAAGAGAACGATCTCAAGATGACGAACTAGCATTAGCTTCTG TGAATTGT CTTCATGGGTTAACACGGACTATCGTGTCCATCCAAAATCTGATAGAATCTGCTAGATCC AAGATGAA

AGCTCCGCATCAGGTAAGTATTTCCACTGGAGATGAATCTGTGCTTGCAAATGGGAT ACTGGCAGAGT CTCTGGCTGAGCTAACATCTGTGTCGTGCTCTTTTAGAGATTCTGTTTCATCAGAATGGC CCATCGTG CAATCAATTGAGCTACATAAACGAGGCGAATTGGCCCCCGGCGTTGGACTTGGTTGGGGA GCTAGCGG TGGTGGGTTTTGGTCAACCAGAGTTCTGTTGGCACAGGCTGGTGCCGGTCTTCTGAGTCT CTTTCTTA ACATCTCTCTGAGCGACTCGCAGAATGATCAGGGATCTGTTGGCTTTATGGATAAAGTAA ACTCCGCT TTAGCTATGTGTTTGATTGCAGGTCCAAGGGATTATTTACTCGTGGAAAGAGCCTTTGAA TATGTCCT TAGACCGCATGCTTTAGAACACCTGGCCTGCTGTATCAAGTCAAACAAAAAAAACATATC GTTTGAAT GGGAATGCAGCGAAGGGGACTATCATCGTATGAGCAGTATGCTTGCTTCTCACTTCAGAC ATAGATGG TTACAGCAAAAGGGAAGATCGATAGCCGAGGAAGGGGTCAGTGGGGTAAGGAAGGGCACA GTTGGTCT GGAGACTATTCATGAGGACGGTGAAATGTCAAATAGTTCAACTCAGGATAAAAAATCAGA CTCCTCGA

CCATAGAGTGGGCTCACCAGAGAATGCCCCTACCTCCACACTGGTTTCTCAGCGCCA TCTCAGCAGTC CACAGTGGTAAAACCTCAACAGGGCCACCAGAATCCACAGAGTTGCTTGAAGTTGCAAAA GCTGGAGT TTTCTTTCTTGCAGGACTTGAGTCATCGTCTGGTTTTGGATCGCTTCCCTCTCCTGTTGT GAGTGTAC CGTTGGTTTGGAAGTTTCACGCTTTGTCTACCGTATTGCTTGTTGGAATGGACATCATCG AAGACAAG AACACTAGGAACTTGTACAATTATCTGCAGGAGCTTTATGGGCAGTTTCTTGATGAAGCG AGACTAAA TCACCGTGACACTGAGCTTCTGAGGTTCAAGTCAGACATTCATGAGAACTACTCTACTTT TCTGGAGA TGGTGGTGGAGCAGTATGCTGCGGTGTCATATGGTGATGTAGTGTATGGCCGGCAGGTCT CGGTTTAC CTGCATCAATGCGTGGAACACTCTGTTCGGCTTTCGGCATGGACAGTGCTCTCCAATGCC CGTGTTCT CGAGCTTCTGCCGAGTCTAGACAAGTGCTTGGGAGAAGCGGATGGTTACCTCGAACCTGT TGAGGAAA ATGAGGCCGTCCTTGAGGCCTACCTGAAGTCATGGACTTGTGGGGCATTGGACAGAGCTG CGACGCGT GGATCAGTAGCCTATACGCTGGTTGTGCATCACTTTTCATCTTTAGTCTTTTGCAACCAA GCCAAGGA TAAAGTATCCCTGCGGAATAAGATTGTCAAGACTCTTGTCAGGGATTTATCAAGAAAGCG GCATCGTG AGGGGATGATGTTAGATCTCCTGCGGTATAAGAAAGGGTCTGCGAACGCCATGGAAGAAG AAGTGATA GCAGCGGAGACAGAGAAAAGAATGGAGGTGTTGAAAGAGGGTTGCGAAGGGAACTCCACC CTCCTCTT GGAACTGGAGAAGCTGAAATCAGCCGCTCTCTGTGGAAGAAGGTGA

SEQ ID NO: 3 Arabidopsis thaliana nucleic acid sequence mutant iyo-2 ATGGAGCAAAGTAGCGGGAGAGTCAATCCGGAACAGCCGAACAACGTCTTGGCGAGCCTT GTCGGGAG CATCGTGGAGAAAGGAATATCGGAGAATAAGCCTCCAAGCAAGCCGCTTCCCCCAAGGCC CTCCCTTC TTTCCTTCCCCGTCGCTCGTCATCGTTCTCACGGACCCCATTTGGCTCCTGTGGGAAGCA GCATAGCA CAACCTAAGGATTACAATGACGATCAGGAAGAAGAAGAAGCAGAAGAACGTTTCATGAAT GCAGACTC

C [T-DNA, Salk 099873- ] TTGCTGCTTTTGCTAAACCGCTTCAAAGAAAAGAGAAGAAAGACATGGACCTCGGGAGGT GGAAAGA TATGGTCTCTGGGGATGATCCTGCATCCACACATGTCCCTCAGCAATCAAGGAAACTTAA GATCATTG AAACGAGACCGCCCTATGTTGCTTCAGCCGATGCGGCCACTACATCCAGCAACACTTTAC TGGCTGCC AGGGCATCAGACCAGAGAGAGTTTGTTTCTGATAAAGCACCGTTTATTAAAAATTTGGGA ACCAAGGA AAGGGTTCCTTTAAACGCTTCTCCTCCCCTAGCTGTTTCGAATGGACTTGGGACTCGACA CGCGTCTT CGTCTCTTGAAAGTGATATTGATGTTGAGAACCATGCAAAGTTGCAGACAATGTCACCCG ACGAGATT

GCTGAGGCTCAGGCTGAGTTATTGGACAAGATGGATCCTGCACTACTCTCCATTTTG AAGAAACGAGG TGAGGCAAAATTGAAGAAGCGAAAGCATTCTGTGCAGGGGGTTTCCATCACCGATGAAAC AGCAAAGA ATTCAAGAACTGAGGGTCATTTTGTCACTCCTAAAGTGATGGCAATACCGAAAGAAAAAA GTGTGGTG CAAAAGCCAGGGATAGCCCAAGGATTCGTGTGGGATGCATGGACTGAGAGGGTTGAGGCA GCCAGAGA CTTGAGATTTTCTTTTGACGGGAATGTTGTTGAGGAAGATGTTGTCTCGCCAGCTGAAAC TGGTGGAA

AGTGGTCTGGTGTTGAATCTGCTGCCGAACGTGATTTCTTGAGAACCGAGGGGGATC CTGGGGCCGCA GGTTACACTATCAAAGAAGCTATTGCTCTTGCACGAAGTGTGATTCCCGGGCAGAGATGT CTTGCTTT GCATCTGCTTGCATCTGTACTCGACAAAGCTTTGAACAAACTTTGTCAAAGCAGAATAGG CTACGCAA GGGAAGAAAAAGATAAATCCACTGACTGGGAAGCCATCTGGGCTTATGCCCTTGGACCGG AACCTGAG CTTGTCTTAGCATTGAGGATGGCTCTTGATGACAACCATGCCTCTGTTGTTATAGCATGT GTAAAAGT

GATTCAGTGTCTACTGAGCTGTTCTCTTAACGAGAATTTCTTTAATATTCTGGAGAA CATGGGACCAC ACGGGAAAGATATCTTCACGGCCTCGGTGTTCAGGAGTAAGCCGGAAATTGATCTTGGCT TCCTCCGT GGTTGCTACTGGAAGTACAGCGCTAAACCCTCCAATATTGTTGCGTTCCGTGAAGAAATC TTGGATGA CGGGACAGAAGATACGGATACTATTCAGAAAGATGTTTTTGTAGCCGGACAAGATGTTGC TGCTGGTC TCGTCAGAATGGATATCCTTCCAAGAATTTATCACCTTCTGGAGACAGAACCAACAGCAG CGCTTGAG

GACAGCATAATCTCTGTTACTATTGCGATAGCAAGGCATTCTCCAAAATGCACAACT GCAATCTTGAA GTATCCCAAATTTGTGCAAACAATTGTGAAAAGATTCCAATTGAACAAAAGAATGGACGT TCTTTCTT CTCAGATCAACTCTGTCCGCCTCTTAAAGGTGTTGGCCCGGTATGATCAAAGTACTTGCA TGGAATTT GTGAAGAATGGGACTTTCAATGCGGTCACATGGCATTTGTTTCAGTTCACCTCATCTCTT GACTCATG GGTGAAGCTAGGGAAGCAGAACTGCAAGCTTTCATCTACCTTGATGGTTGAACAGCTCCG GTTTTGGA AGGTCTGTATCCATAGTGGCTGTTGCGTATCTCGCTTCCCAGAGCTATTCCCAGCTCTGT GTCTGTGG TTGAGTTGTCCATCATTCGAAAAGCTCAGGGAGAAAAATCTCATCAGCGAGTTTACTTCT GTGTCAAA CGAGGCCTACCTGGTCCTTGAGGCTTTTGCCGAGACACTTCCTAATATGTACTCACAAAA CATTCCAC GGAATGAATCTGGGACATGGGACTGGAGCTATGTTAGCCCTATGATTGATTCAGCACTGA GTTGGATA ACATTGGCCCCGCAATTACTCAAGTGGGAGAAAGGAATCGAAAGTGTCTCTGTATCAACT ACTACTCT

GTTGTGGTTGTATTCAGGTGTCATGCGTACAATTTCCAAAGTCCTTGAGAAAATCTC TGCGGAGGGAG AGGAAGAACCTCTACCATGGCTACCGGAGTTTGTTCCAAAGATTGGCCTTGCCATTATCA AGCACAAG CTTCTTAGTTTTTCTGTTGCAGACGTAAGTAGGTTTGGAAAAGACTCTTCCAGGTGTTCC TCTTTTAT GGAGTATTTGTGTTTTCTAAGAGAACGATCTCAAGATGACGAACTAGCATTAGCTTCTGT GAATTGTC TTCATGGGTTAACACGGACTATCGTGTCCATCCAAAATCTGATAGAATCTGCTAGATCCA AGATGAAA GCTCCGCATCAGGTAAGTATTTCCACTGGAGATGAATCTGTGCTTGCAAATGGGATACTG GCAGAGTC TCTGGCTGAGCTAACATCTGTGTCGTGCTCTTTTAGAGATTCTGTTTCATCAGAATGGCC CATCGTGC AATCAATTGAGCTACATAAACGAGGCGGATTGGCCCCCGGCGTTGGACTTGGTTGGGGAG CTAGCGGT GGTGGGTTTTGGTCAACCAGAGTTCTGTTGGCACAGGCTGGTGCCGGTCTTCTGAGTCTC TTTCTTAA CATCTCTCTGAGCGACTCGCAGAATGATCAGGGATCTGTTGGCTTTATGGATAAAGTAAA CTCCGCTT TAGCTATGTGTTTGATTGCAGGTCCAAGGGATTATTTACTCGTGGAAAGAGCCTTTGAAT ATGTCCTT AGACCGCATGCTTTAGAACACCTGGCCTGCTGTATCAAGTCAAACAAAAAAAACATATCG TTTGAATG GGAATGCAGCGAAGGGGACTATCATCGTATGAGCAGTATGCTTGCTTCTCACTTCAGACA TAGATGGT TACAGCAAAAGGGAAGATCGATAGCCGAGGAAGGGGTCAGTGGGGTAAGGAAGGGCACAG TTGGTCTG GAGACTATTCATGAGGACGGTGAAATGTCAAATAGTTCAACTCAGGATAAAAAATCAGAC TCCTCGAC CATAGAGTGGGCTCACCAGAGAATGCCCCTACCTCCACACTGGTTTCTCAGCGCCATCTC AGCAGTCC ACAGTGGTAAAACCTCAACAGGGCCACCAGAATCCACAGAGTTGCTTGAAGTTGCAAAAG CTGGAGTT TTCTTTCTTGCAGGACTTGAGTCATCGTCTGGTTTTGGATCGCTTCCCTCTCCTGTTGTG AGTGTACC GTTGGTTTGGAAGTTTCACGCTTTGTCTACCGTATTGCTTGTTGGAATGGACATCATCGA AGACAAGA ACACTAGGAACTTGTACAATTATCTGCAGGAGCTTTATGGGCAGTTTCTTGATGAAGCGA GACTAAAT CACCGTGACACTGAGCTTCTGAGGTTCAAGTCAGACATTCATGAGAACTACTCTACTTTT CTGGAGAT GGTGGTGGAGCAGTATGCTGCGGTGTCATATGGTGATGTAGTGTATGGCCGGCAGGTCTC GGTTTACC TGCATCAATGCGTGGAACACTCTGTTCGGCTTTCGGCATGGACAGTGCTCTCCAATGCCC GTGTTCTC GAGCTTCTGCCGAGTCTAGACAAGTGCTTGGGAGAAGCGGATGGTTACCTCGAACCTGTT GAGGAAAA TGAGGCCGTCCTTGAGGCCTACCTGAAGTCATGGACTTGTGGGGCATTGGACAGAGCTGC GACGCGTG GATCAGTAGCCTATACGCTGGTTGTGCATCACTTTTCATCTTTAGTCTTTTGCAACCAAG CCAAGGAT AAAGTATCCCTGCGGAATAAGATTGTCAAGACTCTTGTCAGGGATTTATCAAGAAAGCGG CATCGTGA GGGGATGATGTTAGATCTCCTGCGGTATAAGAAAGGGTCTGCGAACGCCATGGAAGAAGA AGTGATAG

CAGCGGAGACAGAGAAAAGAATGGAGGTGTTGAAAGAGGGTTGCGAAGGGAACTCCA CCCTCCTCTTG GAACTGGAGAAGCTGAAATCAGCCGCTCTCTGTGGAAGAAGGTGA

SEQ ID NO: 4 Arabidopsis thaliana nucleic acid sequence mutant iyo-3

ATGGAGCAAAGTAGCGGGAGAGTCAATCCGGAACAGCCGAACAACGTCTTGGCGAGC CTTGTCGGGAG CATCGTGGAGAAAGGAATATCGGAGAATAAGCCTCCAAGCAAGCCGCTTCCCCCAAGGCC CTCCCTTC TTTCCTTCCCCGTCGCTCGTCATCGTTCTCACGGACCCCATTTGGCTCCTGTGGGAAGCA GCATAGCA CAACCTAAGGATTACAATGACGATCAGGAAGAAGAAGAAGCAGAAGAACGTTTCATGAAT GCAGACTC

CATTGCTGCTTTTGCTAAACCGCTTCAAAGAAAAGAGAAGAAAGACATGGACCTCGG GAGGTGGAAAG ATATGGTCTCTGGGGATGATCCTGCATCCACACATGTCCCTCAGCAATCAAGGAAACTTA AGATCATT GAAACGAGACCGCCCTATGTTGCTTCAGCCGATGCGGCCACTACATCCAGCAACACTTTA CTGGCTGC CAGGGCATCAGACCAGAGAGAGTTTGTTTCTGATAAAGCACCGTTTATTAAAAATTTGGG AACCAAGG AAAGGGTTCCTTTAAACGCTTCTCCTCCCCTAGCTGTTTCGAATGGACTTGGGACTCGAC ACGCGTCT

TCGTCTCTTGAAAGTGATATTGATGTTGAGAACCATGCAAAGTTGCAGACAATGTCA CCCGACGAGAT TGCTGAGGCTCAGGCTGAGTTATTGGACAAGATGGATCCTGCACTACTCTCCATTTTGAA GAAACGAG GTGAGGCAAAATTGAAGAAGCGAAAGCATTCTGTGCAGGGGGTTTCCATCACCGATGAAA CAGCAAAG AATTCAAGAACTGAGGGTCATTTTGTCACTCCTAAAGTGATGGCAATACCGAAAGAAAAA AGTGTGGT GCAAAAGCCAGGGATAGCCCAAGGATTCGTGTGGGATGCATGGACTGAGAGGGTTGAGGC AGCCAGAG ACTTGAGATTTTCTTTTGACGGGAATGTTGTTGAGGAAGATGTTGTCTCGCCAGCTGAAA CTGGTGGA AAGTGGTCTGGTGTTGAATCTGCTGCCGAACGTGATTTCTTGAGAACCGAGGGGGATCCT GGGGCCGC AGGTTACACTATCAAAGAAGCTATTGCTCTTGCACGAAGTGTGATTCCCGGGCAGAGATG TCTTGCTT TGCATCTGCTTGCATCTGTACTCGACAAAGCTTTGAACAAACTTTGTCAAAGCAGAATAG GCTACGCA AGGGAAGAAAAAGATAAATCCACTGACTGGGAAGCCATCTGGGCTTATGCCCTTGGACCG GAACCTGA

GCTTGTCTTAGCATTGAGGATGGCTCTTGATGACAACCATGCCTCTGTTGTTATAGC ATGTGTA [ T- DNA

salk692_gl2] AAAGTGATTCAGTGTCTACTGAGCTGTTCTCTTAACGAGAATTTCTTTAATATTCT GGAGAACATGGGACCACACGGGAAAGATATCTTCACGGCCTCGGTGTTCAGGAGTAAGCC GGAAATTG ATCTTGGCTTCCTCCGTGGTTGCTACTGGAAGTACAGCGCTAAACCCTCCAATATTGTTG CGTTCCGT GAAGAAATCTTGGATGACGGGACAGAAGATACGGATACTATTCAGAAAGATGTTTTTGTA GCCGGACA AGATGTTGCTGCTGGTCTCGTCAGAATGGATATCCTTCCAAGAATTTATCACCTTCTGGA GACAGAAC CAACAGCAGCGCTTGAGGACAGCATAATCTCTGTTACTATTGCGATAGCAAGGCATTCTC CAAAATGC ACAACTGCAATCTTGAAGTATCCCAAATTTGTGCAAACAATTGTGAAAAGATTCCAATTG AACAAAAG AATGGACGTTCTTTCTTCTCAGATCAACTCTGTCCGCCTCTTAAAGGTGTTGGCCCGGTA TGATCAAA GTACTTGCATGGAATTTGTGAAGAATGGGACTTTCAATGCGGTCACATGGCATTTGTTTC AGTTCACC TCATCTCTTGACTCATGGGTGAAGCTAGGGAAGCAGAACTGCAAGCTTTCATCTACCTTG ATGGTTGA ACAGCTCCGGTTTTGGAAGGTCTGTATCCATAGTGGCTGTTGCGTATCTCGCTTCCCAGA GCTATTCC CAGCTCTGTGTCTGTGGTTGAGTTGTCCATCATTCGAAAAGCTCAGGGAGAAAAATCTCA TCAGCGAG TTTACTTCTGTGTCAAACGAGGCCTACCTGGTCCTTGAGGCTTTTGCCGAGACACTTCCT AATATGTA CTCACAAAACATTCCACGGAATGAATCTGGGACATGGGACTGGAGCTATGTTAGCCCTAT GATTGATT CAGCACTGAGTTGGATAACATTGGCCCCGCAATTACTCAAGTGGGAGAAAGGAATCGAAA GTGTCTCT GTATCAACTACTACTCTGTTGTGGTTGTATTCAGGTGTCATGCGTACAATTTCCAAAGTC CTTGAGAA AATCTCTGCGGAGGGAGAGGAAGAACCTCTACCATGGCTACCGGAGTTTGTTCCAAAGAT TGGCCTTG CCATTATCAAGCACAAGCTTCTTAGTTTTTCTGTTGCAGACGTAAGTAGGTTTGGAAAAG ACTCTTCC AGGTGTTCCTCTTTTATGGAGTATTTGTGTTTTCTAAGAGAACGATCTCAAGATGACGAA CTAGCATT AGCTTCTGTGAATTGTCTTCATGGGTTAACACGGACTATCGTGTCCATCCAAAATCTGAT AGAATCTG CTAGATCCAAGATGAAAGCTCCGCATCAGGTAAGTATTTCCACTGGAGATGAATCTGTGC TTGCAAAT GGGATACTGGCAGAGTCTCTGGCTGAGCTAACATCTGTGTCGTGCTCTTTTAGAGATTCT GTTTCATC AGAATGGCCCATCGTGCAATCAATTGAGCTACATAAACGAGGCGGATTGGCCCCCGGCGT TGGACTTG GTTGGGGAGCTAGCGGTGGTGGGTTTTGGTCAACCAGAGTTCTGTTGGCACAGGCTGGTG CCGGTCTT CTGAGTCTCTTTCTTAACATCTCTCTGAGCGACTCGCAGAATGATCAGGGATCTGTTGGC TTTATGGA TAAAGTAAACTCCGCTTTAGCTATGTGTTTGATTGCAGGTCCAAGGGATTATTTACTCGT GGAAAGAG

CCTTTGAATATGTCCTTAGACCGCATGCTTTAGAACACCTGGCCTGCTGTATCAAGT CAAACAAAAAA AACATATCGTTTGAATGGGAATGCAGCGAAGGGGACTATCATCGTATGAGCAGTATGCTT GCTTCTCA CTTCAGACATAGATGGTTACAGCAAAAGGGAAGATCGATAGCCGAGGAAGGGGTCAGTGG GGTAAGGA AGGGCACAGTTGGTCTGGAGACTATTCATGAGGACGGTGAAATGTCAAATAGTTCAACTC AGGATAAA AAATCAGACTCCTCGACCATAGAGTGGGCTCACCAGAGAATGCCCCTACCTCCACACTGG TTTCTCAG

CGCCATCTCAGCAGTCCACAGTGGTAAAACCTCAACAGGGCCACCAGAATCCACAGA GTTGCTTGAAG TTGCAAAAGCTGGAGTTTTCTTTCTTGCAGGACTTGAGTCATCGTCTGGTTTTGGATCGC TTCCCTCT CCTGTTGTGAGTGTACCGTTGGTTTGGAAGTTTCACGCTTTGTCTACCGTATTGCTTGTT GGAATGGA CATCATCGAAGACAAGAACACTAGGAACTTGTACAATTATCTGCAGGAGCTTTATGGGCA GTTTCTTG ATGAAGCGAGACTAAATCACCGTGACACTGAGCTTCTGAGGTTCAAGTCAGACATTCATG AGAACTAC

TCTACTTTTCTGGAGATGGTGGTGGAGCAGTATGCTGCGGTGTCATATGGTGATGTA GTGTATGGCCG GCAGGTCTCGGTTTACCTGCATCAATGCGTGGAACACTCTGTTCGGCTTTCGGCATGGAC AGTGCTCT CCAATGCCCGTGTTCTCGAGCTTCTGCCGAGTCTAGACAAGTGCTTGGGAGAAGCGGATG GTTACCTC GAACCTGTTGAGGAAAATGAGGCCGTCCTTGAGGCCTACCTGAAGTCATGGACTTGTGGG GCATTGGA CAGAGCTGCGACGCGTGGATCAGTAGCCTATACGCTGGTTGTGCATCACTTTTCATCTTT AGTCTTTT

GCAACCAAGCCAAGGATAAAGTATCCCTGCGGAATAAGATTGTCAAGACTCTTGTCA GGGATTTATCA AGAAAGCGGCATCGTGAGGGGATGATGTTAGATCTCCTGCGGTATAAGAAAGGGTCTGCG AACGCCAT GGAAGAAGAAGTGATAGCAGCGGAGACAGAGAAAAGAATGGAGGTGTTGAAAGAGGGTTG CGAAGGGA ACTCCACCCTCCTCTTGGAACTGGAGAAGCTGAAATCAGCCGCTCTCTGTGGAAGAAGGT GA

SEQ ID NO: 5 Arabidopsis thaliana Protein MINIYO

MEQSSGRVNPEQPNNVLASLVGS IVEKGI SENKPPSKPLPPRPSLLSFPVARHRSHGPHLAPVGSSIA QPKDYNDDQEEEEAEERFMNADS IAAFAKPLQRKEKKDMDLGRWKDMVSGDDPASTHVPQQSRKLKI I ETRPPYVASADAATTSSNTLLAARASDQREFVSDKAPFIKNLGTKERVPLNASPPLAVSN GLGTRHAS

SSLESDIDVENHAKLQTMSPDEIAEAQAELLDKMDPALLSILKKRGEAKLKKRKHSV QGVS ITDETAK NSRTEGHFVTPKVMAIPKEKSVVQKPGIAQGFVWDAWTERVEAARDLRFSFDGNVVEEDV VSPAETGG KWSGVESAAERDFLRTEGDPGAAGYTIKEAIALARSVIPGQRCLALHLLASVLDKALNKL CQSRIGYA REEKDKSTDWEAIWAYALGPEPELVLALRMALDDNHASVVIACVKVIQCLLSCSLNENFF NILENMGP HGKDIFTASVFRSKPEIDLGFLRGCYWKYSAKPSNIVAFREEILDDGTEDTDTIQKDVFV AGQDVAAG LVRMDILPRIYHLLETEPTAALEDS I I SVTIAIARHSPKCTTAILKYPKFVQTIVKRFQLNKRMDVLS SQINSVRLLKVLARYDQSTCMEFVKNGTFNAVTWHLFQFTSSLDSWVKLGKQNCKLSSTL MVEQLRFW KVCIHSGCCVSRFPELFPALCLWLSCPSFEKLREKNLISEFTSVSNEAYLVLEAFAETLP NMYSQNIP RNESGTWDWSYVSPMIDSALSWITLAPQLLKWEKGIESVSVSTTTLLWLYSGVMRTI SKVLEKISAEG EEEPLPWLPEFVPKIGLAI IKHKLLSFSVADVSRFGKDSSRCSSFMEYLCFLRERSQDDELALASVNC LHGLTRTIVSIQNLIESARSKMKAPHQVS ISTGDESVLANGILAESLAELTSVSCSFRDSVSSEWPIV QSIELHKRGGLAPGVGLGWGASGGGFWSTRVLLAQAGAGLLSLFLNISLSDSQNDQGSVG FMDKVNSA LAMCLIAGPRDYLLVERAFEYVLRPHALEHLACCIKSNKKNISFEWECSEGDYHRMSSML ASHFRHRW LQQKGRS IAEEGVSGVRKGTVGLETIHEDGEMSNSSTQDKKSDSSTIEWAHQRMPLPPHWFLSAI SAV HSGKTSTGPPESTELLEVAKAGVFFLAGLESSSGFGSLPSPVVSVPLVWKFHALSTVLLV GMDI IEDK NTRNLYNYLQELYGQFLDEARLNHRDTELLRFKSDIHENYSTFLEMVVEQYAAVSYGDVV YGRQVSVY LHQCVEHSVRLSAWTVLSNARVLELLPSLDKCLGEADGYLEPVEENEAVLEAYLKSWTCG ALDRAATR GSVAYTLVVHHFSSLVFCNQAKDKVSLRNKIVKTLVRDLSRKRHREGMMLDLLRYKKGSA AMEEEVI AAETEKRMEVLKEGCEGNSTLLLELEKLKSAALCGRR

SEQ ID NO: 6 Arabidopsis thaliana, protein allele iyo-1

MEQSSGRVNPEQPNNVLASLVGS IVEKGI SENKPPSKPLPPRPSLLSFPVARHRSHGPHLAPVGSSIA QPKDYNDDQEEEEAEERFMNADS IAAFAKPLQRKEKKDMDLGRWKDMVSGDDPASTHVPQQSRKLKI I ETRPPYVASADAATTSSNTLLAARASDQREFVSDKAPFIKNLGTKERVPLNASPPLAVSN GLGTRHAS SSLESDIDVENHAKLQTMSPDEIAEAQAELLDKMDPALLSILKKRGEAKLKKRKHSVQGV S ITDETAK NSRTEGHFVTPKVMAIPKEKSVVQKPGIAQGFVWDAWTERVEAARDLRFSFDGNVVEEDV VSPAETGG

KWSGVESAAERDFLRTEGDPGAAGYTIKEAIALARSVIPGQRCLALHLLASVLDKAL NKLCQSRIGYA REEKDKSTDWEAIWAYALGPEPELVLALRMALDDNHASVVIACVKVIQCLLSCSLNENFF NILENMGP HGKDIFTASVFRSKPEIDLGFLRGCYWKYSAKPSNIVAFREEILDDGTEDTDTIQKDVFV AGQDVAAG LVRMDILPRIYHLLETEPTAALEDS I I SVTIAIARHSPKCTTAILKYPKFVQTIVKRFQLNKRMDVLS SQINSVRLLKVLARYDQSTCMEFVKNGTFNAVTWHLFQFTSSLDSWVKLGKQNCKLSSTL MVEQLRFW

KVCIHSGCCVSRFPELFPALCLWLSCPSFEKLREKNLISEFTSVSNEAYLVLEAFAE TLPNMYSQNIP RNESGTWDWSYVSPMIDSALSWITLAPQLLKWEKGIESVSVSTTTLLWLYSGVMRTI SKVLEKISAEG EEEPLPWLPEFVPKIGLAI IKHKLLSFSVADVSRFGKDSSRCSSFMEYLCFLRERSQDDELALASVNC LHGLTRTIVSIQNLIESARSKMKAPHQVS ISTGDESVLANGILAESLAELTSVSCSFRDSVSSEWPIV QSIELHKRGELAPGVGLGWGASGGGFWSTRVLLAQAGAGLLSLFLNI SLSDSQNDQGSVGFMDKVNSA

LAMCLIAGPRDYLLVERAFEYVLRPHALEHLACCIKSNKKNISFEWECSEGDYHRMS SMLASHFRHRW LQQKGRS IAEEGVSGVRKGTVGLETIHEDGEMSNSSTQDKKSDSSTIEWAHQRMPLPPHWFLSAI SAV HSGKTSTGPPESTELLEVAKAGVFFLAGLESSSGFGSLPSPVVSVPLVWKFHALSTVLLV GMDI IEDK NTRNLYNYLQELYGQFLDEARLNHRDTELLRFKSDIHENYSTFLEMVVEQYAAVSYGDVV YGRQVSVY LHQCVEHSVRLSAWTVLSNARVLELLPSLDKCLGEADGYLEPVEENEAVLEAYLKSWTCG ALDRAATR

GSVAYTLVVHHFSSLVFCNQAKDKVSLRNKIVKTLVRDLSRKRHREGMMLDLLRYKK GSANAMEEEVI AAETEKRMEVLKEGCEGNSTLLLELEKLKSAALCGRR

SEQ ID No. 7 MINIYO nucleic acid sequence Arabidopsis thaliana

AAAGAGTTTTCCGTTTTGCTGAGCGGAGGCGAGAGAGGGTTTAGAGTGATGGAGCAA AGTAGCGGGAG AGTCAATCCGGAACAGCCGAACAACGTCTTGGCGAGCCTTGTCGGGAGCATCGTGGAGAA AGGAATAT CGGAGAATAAGCCTCCAAGCAAGCCGCTTCCCCCAAGGCCCTCCCTTCTTTCCTTCCCCG TCGCTCGT CATCGTTCTCACGGACCCGTAAGCCAATCCAATCCTCTAGTGCGTGCTTTTTAGGTTTCC ATCTTCCT TTTGTTGCCTTCTTCTAGATTTTAAGCACCTTCTACTGTTGTTTAGTACTTGGGACTCCA CAATTTTT CACCGTGCCTGACCTTGTAATTCAGCTTTCTGAGACATCTAATTTTTGTTTCTCATGTTT GATTTTGT AGCATTTGGCTCCTGTGGGAAGCAGCATAGCACAACCTAAGGATTACAATGACGATCAGG AAGAAGAA GAAGCAGAAGAACGTTTCATGAATGCAGACTCCATTGCTGCTTTTGCTAAACCGCTTCAA AGAAAAGA GAAGAAAGACATGGACCTCGGGAGGTGGAAAGATATGGTCTCTGGGGATGATCCTGCATC CACACATG TCCCTCAGCAATCAAGGAAACTTAAGATCATTGAAACGAGACCGCCCTATGTTGCTTCAG CCGATGCG GCCACTACATCCAGCAACACTTTACTGGCTGCCAGGGCATCAGACCAGAGAGAGTTTGTT TCTGATAA AGCACCGTTTATTAAAAATTTGGGAACCAAGGAAAGGGTTCCTTTAAACGCTTCTCCTCC CCTAGCTG TTTCGAATGGACTTGGGACTCGACACGCGTCTTCGTCTCTTGAAAGTGATATTGATGTTG AGAACCAT GCAAAGTTGCAGACAATGTCACCCGACGAGATTGCTGAGGCTCAGGCTGAGTTATTGGAC AAGATGGA TCCTGCACTACTCTCCATTTTGAAGAAACGAGGTGAGGCAAAATTGAAGAAGCGAAAGCA TTCTGTGC AGGGGGTTTCCATCACCGATGAAACAGCAAAGAATTCAAGAACTGAGGGTCATTTTGTCA CTCCTAAA GTGATGGCAATACCGAAAGAAAAAAGTGTGGTGCAAAAGCCAGGGATAGCCCAAGGATTC GTGTGGGA TGCATGGACTGAGAGGGTTGAGGCAGCCAGAGACTTGAGATTTTCTTTTGACGGGAATGT TGTTGAGG AAGATGTTGTCTCGCCAGCTGAAACTGGTGAGTAGAACAATACAACTGAAACACATGACA ATCTTAGG TTGCTTACACTTTGACTGTACAGGTGGAAAGTGGTCTGGTGTTGAATCTGCTGCCGAACG TGATTTCT TGAGAACCGAGGGGGATCCTGGGGCCGCAGGTTACACTATCAAAGAAGCTATTGCTCTTG CACGAAGT GTGGTATGTATGATTGCCACATATTTTAATTTTGATGCTAATTAATGGTTAAATTCTTTT TTCCCTCC ATTTTGGCTTTAGCTGAACAAAACCTGTAGGCTGAGACTGCGTTTTTTTCGTTATCACTG CTCATTGA TTTGTATGTATTATTGATATATATATCAGATTCCCGGGCAGAGATGTCTTGCTTTGCATC TGCTTGCA TCTGTACTCGACAAAGCTTTGAACAAACTTTGTCAAAGCAGAATAGGCTACGCAAGGGAA GAAAAAGA TAAATCCACTGACTGGGAAGCCATCTGGGCTTATGCCCTTGGACCGGAACCTGAGCTTGT CTTAGCAT TGAGGTAATTTCCTGATGGGTGTAATTTTGAGACTTATTTGTGAAGTTGTCACTCATAAA TCATAAAT TGTTTGTTCTTATCAATATAAGTTTCTTTTCTTCTTTAGGATGGCTCTTGATGACAACCA TGCCTCTG TTGTTATAGCATGTGTAAAAGTGATTCAGTGTCTACTGAGCTGTTCTCTTAACGAGAATT TCTTTAAT ATTCTGGAGGTATAGTTGATTTTTCTCACTCCTAAGAAGTTATAGTCCTCATAGAACGTG ATTATACA TGTTCAAACTGATAAAACCCATTTCTATTTCCAGAACATGGGACCACACGGGAAAGATAT CTTCACGG CCTCGGTGTTCAGGAGTAAGCCGGAAATTGATCTTGGCTTCCTCCGTGGTTGCTACTGGA AGTACAGC

GCTAAACCCTCCAATATTGTTGCGTTCCGTGAAGAAATCTTGGATGACGGGACAGAA GATACGGATAC TATTCAGAAAGATGTTTTTGTAGCCGGACAAGATGTTGCTGCTGGTCTCGTCAGAATGGA TATCCTTC CAAGAATTTATCACCTTCTGGAGGTGAGATCACTATCTATGTGTAACTCAGCAAGTAAAA TCATTCTT TTTGTGTCGTTGCTTAGTTTTCTGGTTTTTTTTTAATGTTCATGATTTCAGACAGAACCA ACAGCAGC GCTTGAGGACAGCATAATCTCTGTTACTATTGCGATAGCAAGGCATTCTCCAAAATGCAC AACTGCAA

TCTTGAAGTATCCCAAATTTGTGCAAACAATTGTGAAAAGATTCCAATTGAACAAAA GAATGGACGTT CTTTCTTCTCAGATCAACTCTGTCCGCCTCTTAAAGGTAATACTGGTCCGCTCATACAAA ATTATCTT GGGGTCGTTATATTCATTCGTCTTTGATGTTTTTTTTACAGAACCTGATGATTCGAGTTT GTTAAGCT ATCAATTCTCAGAGCTATTGTAACCTTCGTTCTTCTTTCTCTCTTTTTAATTTCACTAAG GTGTTGGC CCGGTATGATCAAAGTACTTGCATGGAATTTGTGAAGAATGGGACTTTCAATGCGGTCAC ATGGCATT

TGTTTCAGTTCACCTCATCTCTTGACTCATGGGTGAAGCTAGGGAAGCAGAACTGCA AGCTTTCATCT ACCTTGATGGTTGAACAGCTCCGGTTTTGGAAGGTCTGTATCCATAGTGGCTGTTGCGTA TCTCGCTT CCCAGAGCTATTCCCAGCTCTGTGTCTGTGGTTGAGTTGTCCATCATTCGAAAAGCTCAG GGAGAAAA ATCTCATCAGCGAGTTTACTTCTGTGTCAAACGAGGCCTACCTGGTCCTTGAGGCTTTTG CCGAGACA CTTCCTAATATGTACTCACAAAACATTCCACGGAATGAATCTGGGACATGGGACTGGAGC TATGTTAG

CCCTATGATTGATTCAGCACTGAGTTGGATAACATTGGCCCCGCAATTACTCAAGTG GGAGAAAGGAA TCGAAAGTGTCTCTGTATCAACTACTACTCTGTTGTGGTTGTATTCAGGTGTCATGCGTA CAATTTCC AAAGTCCTTGAGAAAATCTCTGCGGAGGGAGAGGAAGAACCTCTACCATGGCTACCGGAG TTTGTTCC AAAGATTGGCCTTGCCATTATCAAGCACAAGCTTCTTAGTTTTTCTGTTGCAGACGTAAG TAGGTTTG GAAAAGACTCTTCCAGGTGTTCCTCTTTTATGGAGTATTTGTGTTTTCTAAGAGAACGAT CTCAAGAT GACGAACTAGCATTAGCTTCTGTGAATTGTCTTCATGGGTTAACACGGACTATCGTGTCC ATCCAAAA TCTGATAGAATCTGCTAGATCCAAGATGAAAGCTCCGCATCAGGTAAGTATTTCCACTGG AGATGAAT CTGTGCTTGCAAATGGGATACTGGCAGAGTCTCTGGCTGAGCTAACATCTGTGTCGTGCT CTTTTAGA GATTCTGTTTCATCAGAATGGCCCATCGTGCAATCAATTGAGCTACATAAACGAGGCGGA TTGGCCCC CGGCGTTGGACTTGGTTGGGGAGCTAGCGGTGGTGGGTTTTGGTCAACCAGAGTTCTGTT GGCACAGG

CTGGTGCCGGTCTTCTGAGTCTCTTTCTTAACATCTCTCTGAGCGACTCGCAGAATG ATCAGGGATCT GTTGGCTTTATGGATAAAGTAAACTCCGCTTTAGCTATGTGTTTGATTGCAGGTCCAAGG GATTATTT ACTCGTGGAAAGAGCCTTTGAATATGTCCTTAGACCGCATGCTTTAGAACACCTGGCCTG CTGTATCA AGTCAAACAAAAAAAACATATCGTTTGAATGGGAATGCAGCGAAGGGGACTATCATCGTA TGAGCAGT ATGCTTGCTTCTCACTTCAGACATAGATGGTTACAGCAAAAGGGAAGATCGATAGCCGAG GAAGGGGT CAGTGGGGTAAGGAAGGGCACAGTTGGTCTGGAGACTATTCATGAGGACGGTGAAATGTC AAATAGTT CAACTCAGGATAAAAAATCAGACTCCTCGACCATAGAGTGGGCTCACCAGAGAATGCCCC TACCTCCA CACTGGTTTCTCAGCGCCATCTCAGCAGTCCACAGTGGTAAAACCTCAACAGGGCCACCA GAATCCAC AGAGTTGCTTGAAGTTGCAAAAGCTGGAGTTTTCTTTCTTGCAGGACTTGAGTCATCGTC TGGTTTTG GATCGCTTCCCTCTCCTGTTGTGAGTGTACCGTTGGTTTGGAAGTTTCACGCTTTGTCTA CCGTATTG CTTGTTGGAATGGACATCATCGAAGACAAGAACACTAGGAACTTGTACAATTATCTGCAG GAGCTTTA TGGGCAGTTTCTTGATGAAGCGAGACTAAATCACCGTGACACTGAGCTTCTGAGGTTCAA GTCAGACA TTCATGAGAACTACTCTACTTTTCTGGAGATGGTGGTGGAGCAGTATGCTGCGGTGTCAT ATGGTGAT GTAGTGTATGGCCGGCAGGTCTCGGTTTACCTGCATCAATGCGTGGAACACTCTGTTCGG CTTTCGGC ATGGACAGTGCTCTCCAATGCCCGTGTTCTCGAGCTTCTGCCGAGTCTAGACAAGTGCTT GGGAGAAG CGGATGGTTACCTCGAACCTGTTGAGGTAATTTACAAAAATAATAAAATGTTGATAGTGG TGAATAAT GGCATCTTGAGCATCCAACTAAGATAAAATGGTGAATTGATATTGCAGGAAAATGAGGCC GTCCTTGA GGCCTACCTGAAGTCATGGACTTGTGGGGCATTGGACAGAGCTGCGACGCGTGGATCAGT AGCCTATA CGCTGGTTGTGCATCACTTTTCATCTTTAGTCTTTTGCAACCAAGCCAAGGATAAAGTAT CCCTGCGG AATAAGATTGTCAAGACTCTTGTCAGGGATTTATCAAGAAAGCGGCATCGTGAGGTAACT TGAAATCC CTCATCTCTTGTTCAATGTCATTCTGGGGACTGAGGATGATAATGAAACGTGGAAATAAT GTTTCAGG GGATGATGTTAGATCTCCTGCGGTATAAGAAAGGGTCTGCGAACGCCATGGAAGAAGAAG TGATAGCA GCGGAGACAGAGAAAAGAATGGAGGTGTTGAAAGAGGGTTGCGAAGGGAACTCCACCCTC CTCTTGGA ACTGGAGAAGCTGAAATCAGCCGCTCTCTGTGGAAGAAGGTGAACGAGAGAATGAGAGGA AAGAAAGT CTGTGTGTTTCTTTCTCTGTTTTGAGGTTCTCTTACAGATGAAAAGCTGTGTAATTAAAA ATCGATGT

TCTTCTTCTGTTCTTGTAAGATTTTGGATTTTTCCAATTTCTGACAAAGTTCAATTA AAAAACTTGAC TGACATTTTGAAA

SEQ ID NO: 8 Arabidopsis thaliana, nucleic acid sequence AtRTRl .

ATGGCAAAGGATAATGAAGCAATCGCCATTAACGATGCGGTTCACAAGCTTCAGCTC TATATGCTCGA AAATACCACTGATCAGAACCAGCTCTTCGCGGCGAGGAAGTTAATGTCTCGATCAGATTA CGAAGATG TCGTCACTGAACGAGCAATCGCTAAGCTCTGTGGTTATACTCTTTGCCAGAGATTTCTCC CTTCCGAT GTTTCTAGAAGAGGGAAGTATCGGATTTCGTTGAAGGACCATAAGGTTTACGATTTACAG GAGACGAG

CAAGTTTTGCTCCGCTGGTTGTTTAATTGATAGCAAAACGTTTTCGGGGAGTTTGCA AGAGGCTCGTA CATTGGAGTTTGATTCGGTGAAGTTGAATGAGATTTTGGATTTGTTTGGTGATTCTTTGG AAGTGAAA GGTTCTTTGGATGTGAATAAGGATTTGGATTTGTCTAAGCTTATGATTAAGGAGAATTTT GGAGTTAG AGGTGAAGAATTGTCTTTAGAGAAGTGGATGGGTCCTTCTAATGCTGTTGAAGGTTATGT TCCTTTTG ATCGAAGCAAATCAAGTAATGATTCCAAGGCTACTACTCAAAGTAATCAAGAGAAGCATG AGATGGAT

TTCACTAGCACAGTAATTATGCCTGATGTTAATAGTGTTTCAAAGCTTCCACCGCAA ACCAAGCAAGC TTCTACTGTTGTGGAATCTGTTGATGGCAAAGGGAAAACAGTTCTGAAAGAGCAAACTGT AGTTCCTC CCACCAAAAAAGTTTCGAGATTTCGTCGTGAGAAAGAAAAGGAGAAGAAGACTTTCGGGG TTGATGGG ATGGGTTGTGCCCAGGAAAAAACTACAGTTCTCCCCAGAAAAATATTGAGTTTTTGTAAT GAAATAGA GAAGGATTTTAAGAATTTTGGGTTTGATGAGATGGGTCTTGCGAGTTCTGCTATGATGAG TGATGGAT

ACGGCGTAGAATATAGTGTGTCTAAGCAGCCACAATGTTCGATGGAAGATTCTCTTA GTTGCAAGCTA AAAGGAGATCTTCAGACTTTGGACGGGAAAAATACCCTATCAGGATCCTCTTCTGGTTCT AATACGAA GGGCTCGAAGACAAAACCAGAGAAATCAAGAAAGAAAATTATTTCTGTTGAATACCATGC TAATTCTT ATGAAGATGGTGAAGAAATCCTTGCAGCTGAATCGTATGAAAGACATAAAGCTCAGGATG TGTGTTCA TCAAGTGAAATCGTCACTAAATCATGCCTTAAAATTTCTGGCTCGAAGAAGCTTAGTCGT TCAGTTAC TTGGGCCGATCAGAATGATGGCCGTGGTGATCTTTGTGAGGTTAGAAACAATGATAACGC AGCAGGTC CTAGCCTGTCTTCTAATGATATAGAGGATGTCAATAGTTTATCACGCCTTGCATTAGCAG AAGCCCTT GCTACGGCATTGAGCCAGGCTGCCGAAGCTGTTTCTTCGGGAAATTCAGATGCAAGTGAT GCCACTGC AAAAGCTGGAATCATTTTGTTGCCCAGCACACATCAACTTGACGAAGAGGTTACTGAGGA ACATAGTG AGGAGGAAATGACTGAAGAGGAACCAACTCTTCTCAAGTGGCCAAATAAGCCCGGGATTC CAGATTCT

GATTTGTTTGACCGTGATCAATCGTGGTTTGATGGACCTCCAGAGGGCTTCAATCTC ACATTATCAAA TTTCGCTGTGATGTGGGATTCACTGTTTGGCTGGGTATCATCGTCCTCTCTGGCATACAT ATATGGGA AGGAAGAATCTGCTCATGAGGAGTTCTTATTGGTTAACGGGAAGGAGTACCCCCGGAGGA TTATCATG GTAGATGGGCTTTCCTCAGAGATCAAGCAGACAATTGCTGGGTGCCTTGCCAGAGCTTTA CCGAGAGT CGTCACTCATCTCAGGCTGCCAATAGCGATATCCGAGTTAGAAAAGGGACTGGGAAGCTT GTTGGAGA CAATGTCGTTGACAGGAGCAGTTCCATCATTTAGGGTAAAAGAATGGCTAGTGATTGTTC TTCTTTTC TTGGATGCGTTGTCTGTATCACGTATCCCTCGGATTGCACCTTATATATCCAACAGAGAC AAGATTTT GGAAGGAAGTGGAATTGGAAATGAAGAGTATGAGACAATGAAGGATATCCTGTTACCACT TGGCCGTG TTCCTCAGTTTGCTACCCGAAGCGGGGCGTAG

SEQ ID NO: 9 Arabidopsis thaliana, Nucleic acid sequence mutant atrtrl-1

ATGGCAAAGGATAATGAAGCAATCGCCATTAACGATGCGGTTCACAAGCTTCAGCTC TATATGCTCGA AAATACCACTGATCAGAACCAGCTCTTCGCGGCGAGGAAGTTAATGTCTCGATCAGATTA CGAAGATG TCGTCACTGAACGAGCAATCGCTAAGCTCTGTGGTTATACTCTTTGCCAGAGATTTCTCC CTTCCGAT GTTTCTAGAAGAGGGAAGTATCGGATTTCGTTGAAGGACCATAAGGTTTACGATTTACAG GAGACGAG CAAGTTTTGCTCCGCTGGTTGTTTAATTGATAGCAAAACGTTTTCGGGGAGTTTGCAAGA GGCTCGTA CATTGGAGTTTGATTCGGTGAAGTTGAATGAGATTTTGGATTTGTTTGGTGATTCTTTGG AAGTGAAA GGTTCT [T-DNA Salk 012339] TTGGATGTGAATAAGGATTTGGATTTGTCTAAGCTTATGATTAAGGAGAATTTTGGAGTT A GAGGTGAAGAATTGTCTTTAGAGAAGTGGATGGGTCCTTCTAATGCTGTTGAAGGTTATG TTCCTTTT GATCGAAGCAAATCAAGTAATGATTCCAAGGCTACTACTCAAAGTAATCAAGAGAAGCAT GAGATGGA TTTCACTAGCACAGTAATTATGCCTGATGTTAATAGTGTTTCAAAGCTTCCACCGCAAAC CAAGCAAG CTTCTACTGTTGTGGAATCTGTTGATGGCAAAGGGAAAACAGTTCTGAAAGAGCAAACTG TAGTTCCT CCCACCAAAAAAGTTTCGAGATTTCGTCGTGAGAAAGAAAAGGAGAAGAAGACTTTCGGG GTTGATGG GATGGGTTGTGCCCAGGAAAAAACTACAGTTCTCCCCAGAAAAATATTGAGTTTTTGTAA TGAAATAG

AGAAGGATTTTAAGAATTTTGGGTTTGATGAGATGGGTCTTGCGAGTTCTGCTATGA TGAGTGATGGA TACGGCGTAGAATATAGTGTGTCTAAGCAGCCACAATGTTCGATGGAAGATTCTCTTAGT TGCAAGCT AAAAGGAGATCTTCAGACTTTGGACGGGAAAAATACCCTATCAGGATCCTCTTCTGGTTC TAATACGA AGGGCTCGAAGACAAAACCAGAGAAATCAAGAAAGAAAATTATTTCTGTTGAATACCATG CTAATTCT TATGAAGATGGTGAAGAAATCCTTGCAGCTGAATCGTATGAAAGACATAAAGCTCAGGAT GTGTGTTC

ATCAAGTGAAATCGTCACTAAATCATGCCTTAAAATTTCTGGCTCGAAGAAGCTTAG TCGTTCAGTTA CTTGGGCCGATCAGAATGATGGCCGTGGTGATCTTTGTGAGGTTAGAAACAATGATAACG CAGCAGGT CCTAGCCTGTCTTCTAATGATATAGAGGATGTCAATAGTTTATCACGCCTTGCATTAGCA GAAGCCCT TGCTACGGCATTGAGCCAGGCTGCCGAAGCTGTTTCTTCGGGAAATTCAGATGCAAGTGA TGCCACTG CAAAAGCTGGAATCATTTTGTTGCCCAGCACACATCAACTTGACGAAGAGGTTACTGAGG AACATAGT

GAGGAGGAAATGACTGAAGAGGAACCAACTCTTCTCAAGTGGCCAAATAAGCCCGGG ATTCCAGATTC TGATTTGTTTGACCGTGATCAATCGTGGTTTGATGGACCTCCAGAGGGCTTCAATCTCAC ATTATCAA ATTTCGCTGTGATGTGGGATTCACTGTTTGGCTGGGTATCATCGTCCTCTCTGGCATACA TATATGGG AAGGAAGAATCTGCTCATGAGGAGTTCTTATTGGTTAACGGGAAGGAGTACCCCCGGAGG ATTATCAT GGTAGATGGGCTTTCCTCAGAGATCAAGCAGACAATTGCTGGGTGCCTTGCCAGAGCTTT ACCGAGAG

TCGTCACTCATCTCAGGCTGCCAATAGCGATATCCGAGTTAGAAAAGGGACTGGGAA GCTTGTTGGAG ACAATGTCGTTGACAGGAGCAGTTCCATCATTTAGGGTAAAAGAATGGCTAGTGATTGTT CTTCTTTT CTTGGATGCGTTGTCTGTATCACGTATCCCTCGGATTGCACCTTATATATCCAACAGAGA CAAGATTT TGGAAGGAAGTGGAATTGGAAATGAAGAGTATGAGACAATGAAGGATATCCTGTTACCAC TTGGCCGT GTTCCTCAGTTTGCTACCCGAAGCGGGGCGTAG

SEQ ID NO: 10

Arabidopsis thaliana, nucleic acid sequence mutant atrtrl-2 ATGGCAAAGGATAATGAAGCAATCGCCATTAACGATGCGGTTCACAAGCTTCAGCTCTAT ATGCTCGA AAATACCACTGATCAGAACCAGCTCTTCGCGGCGAGGAAGTTAATGTCTCGATCAGATTA CGAAGATG TCGTCACTGAACGAGCAATCGCTAAGCTCTGTGGTTATACTCTTTGCCAGAGATTTCTCC CTTCCGAT GTTTCTAGAAGAGGGAAGTATCGGATTTCGTTGAAGGACCATAAGGTTTACGATTTACAG GAGACGAG CAAGTTTTGCTCCGCTGGTTGTTTAATTGATAGCAAAACGTTTTCGGGGAGTTTGCAAGA GGCTCGTA CATTGGAGTTTGATTCGGTGAAGTTGAATGAGATTTTGGATTTGTTTGGTGATTCTTTGG AAGTGAAA GGTTCTTTGGATGTGAATAAGGATTTGGATTTGTCTAAGCTTATGATTAAGGAGAATTTT GGAGTTAG AGGTGAAGAATTGTCTTTAGAGAAGTGGATGGGTCCTTCTAATGCTGTTGAAGGTTATGT TCCTTTTG ATCGAAGCAAATCAAGTAATGATTCCAAGGCTACTACTCAAAGTAATCAAGAGAAGCATG AGATGGAT TTCACTAGCACAGTAATTATGCCTGATGTTAATAGTGTTTCAAAGCTTCCACCGCAAACC AAGCAAGC TTCTACTGTTGTGGAATCTGTTGATGGCAAAGGGAAAACAGTTCTGAAAGAGCAAACTGT AGTTCCTC CCACCAAAAAAGTTTCGAGATTTCGTCGTGAGAAAGAAAAGGAGAAGAAGACTTTCGGGG TTGATGGG ATGGGTTGTGCCCAGGAAAAAACTACAGTTCTCCCCAGAAAAATATTGA [ T-

DNA, Salkll5762] GTTTTTGTAATGAAATAGAGAAGGATTTTAAGAATTTTGGGTTTGATGAGATG GGTCTTGCGAGTTCTGCTATGATGAGTGATGGATACGGCGTAGAATATAGTGTGTCTAAG CAGCCACA ATGTTCGATGGAAGATTCTCTTAGTTGCAAGCTAAAAGGAGATCTTCAGACTTTGGACGG GAAAAATA CCCTATCAGGATCCTCTTCTGGTTCTAATACGAAGGGCTCGAAGACAAAACCAGAGAAAT CAAGAAAG AAAATTATTTCTGTTGAATACCATGCTAATTCTTATGAAGATGGTGAAGAAATCCTTGCA GCTGAATC GTATGAAAGACATAAAGCTCAGGATGTGTGTTCATCAAGTGAAATCGTCACTAAATCATG CCTTAAAA TTTCTGGCTCGAAGAAGCTTAGTCGTTCAGTTACTTGGGCCGATCAGAATGATGGCCGTG GTGATCTT TGTGAGGTTAGAAACAATGATAACGCAGCAGGTCCTAGCCTGTCTTCTAATGATATAGAG GATGTCAA TAGTTTATCACGCCTTGCATTAGCAGAAGCCCTTGCTACGGCATTGAGCCAGGCTGCCGA AGCTGTTT CTTCGGGAAATTCAGATGCAAGTGATGCCACTGCAAAAGCTGGAATCATTTTGTTGCCCA GCACACAT CAACTTGACGAAGAGGTTACTGAGGAACATAGTGAGGAGGAAATGACTGAAGAGGAACCA ACTCTTCT CAAGTGGCCAAATAAGCCCGGGATTCCAGATTCTGATTTGTTTGACCGTGATCAATCGTG GTTTGATG

GACCTCCAGAGGGCTTCAATCTCACATTATCAAATTTCGCTGTGATGTGGGATTCAC TGTTTGGCTGG GTATCATCGTCCTCTCTGGCATACATATATGGGAAGGAAGAATCTGCTCATGAGGAGTTC TTATTGGT TAACGGGAAGGAGTACCCCCGGAGGATTATCATGGTAGATGGGCTTTCCTCAGAGATCAA GCAGACAA TTGCTGGGTGCCTTGCCAGAGCTTTACCGAGAGTCGTCACTCATCTCAGGCTGCCAATAG CGATATCC GAGTTAGAAAAGGGACTGGGAAGCTTGTTGGAGACAATGTCGTTGACAGGAGCAGTTCCA TCATTTAG

GGTAAAAGAATGGCTAGTGATTGTTCTTCTTTTCTTGGATGCGTTGTCTGTATCACG TATCCCTCGGA TTGCACCTTATATATCCAACAGAGACAAGATTTTGGAAGGAAGTGGAATTGGAAATGAAG AGTATGAG ACAATGAAGGATATCCTGTTACCACTTGGCCGTGTTCCTCAGTTTGCTACCCGAAGCGGG GCGTAG SEQ ID NO: 11 Arabidopsis thaliana, Protein sequence AtRTRl

MAKDNEAIAINDAVHKLQLYMLENTTDQNQLFAARKLMSRSDYEDVVTERAIAKLCG YTLCQRFLPSD VSRRGKYRI SLKDHKVYDLQETSKFCSAGCLIDSKTFSGSLQEARTLEFDSVKLNEILDLFGDSLEVK GSLDVNKDLDLSKLMIKENFGVRGEELSLEKWMGPSNAVEGYVPFDRSKSSNDSKATTQS NQEKHEMD FTSTVIMPDVNSVSKLPPQTKQASTVVESVDGKGKTVLKEQTVVPPTKKVSRFRREKEKE KKTFGVDG

MGCAQEKTTVLPRKILSFCNEIEKDFKNFGFDEMGLASSAMMSDGYGVEYSVSKQPQ CSMEDSLSCKL KGDLQTLDGKNTLSGSSSGSNTKGSKTKPEKSRKKI I SVEYHANSYEDGEEILAAESYERHKAQDVCS SSEIVTKSCLKISGSKKLSRSVTWADQNDGRGDLCEVRNNDNAAGPSLSSNDIEDVNSLS RLALAEAL ATALSQAAEAVSSGNSDASDATAKAGI ILLPSTHQLDEEVTEEHSEEEMTEEEPTLLKWPNKPGIPDS DLFDRDQSWFDGPPEGFNLTLSNFAVMWDSLFGWVSSSSLAYIYGKEESAHEEFLLVNGK EYPRRI IM VDGLSSEIKQTIAGCLARALPRVVTHLRLPIAI SELEKGLGSLLETMSLTGAVPSFRVKEWLVIVLLF LDALSVSRIPRIAPYISNRDKILEGSGIGNEEYETMKDILLPLGRVPQFATRSGA

SEQ ID No: 12 MINIYO Oryza sativa ssp. Japonica, Os06g37640.1

MDDAAERRRRQQQQQQPGAAHPARRKVVEEPFDPSPPPAAAVAPPSSRLVGAIVEKG FSSGAAAAAPS SAPSPTVLPFPVARHRSHGPHWKPAARDAAMAEGEGEEEEGMDVDETDYQPVAAAAGPVK RKEKKGMD FSRWREFVADDAPPKRRQAKPLQPKKQTAQKIDTGVVAATTGGTAQEKRSGGIGMQLEVG NGKEELGG AALMSDVAPRKPMKQVDARDDVRNVELRGEGMESDNGEPSLTAEI AENMARLAGMSAGEIAEAQAEI LNRMDPAFVEMLKRRGKEKSGSRKDGGKGKGGGISGPGKISKAMPGEWLSAGEHSGHTWK AWSERVER IRSCRFTLEGDILGFQSCQEQQHVFWYPLHVNLAFPLTGKKAHVETVGERDFLRTEGDPA AVGYTINE AVALSRSMVPGQRVLALQLLALILNRALQNLHKTDLIDNFKESNDDDKFNDWQAVWAYAI GPEPELVL SLRMSLDDNHDSVVLTCAKVINAMLSYEMNEMYFDVLEKVVDQGKDICTAPVFRSKPDQN GGFLEGGF WKYNTKPSNILPHYGENDEEEGDEKHTIQDDVVVSGQDVAAGLVRMGILPRICFLLEMDP HPILEDNL VSILLGLARHSPQSADAILNCPRLVQSVVKLLVKQGSMEIHSSQIKGVNLLKVLSKYNRQ TCFNFVNT GVFHQAMWHWYRKAYTLEDWIRSGKEHCKLTSALMVEQLRFWRTCISYGFCITHFTDFFP ILCLWLSP SMFQKLSESNVVAEFSS IATESYLVLGALAQRLPLLHSVEQLSKQDMGLSGIQVETWSWSHAVPMVDL ALSWLCLNDIPYVCLLI SGQSKNILEGSYFALVISSVLGMLDS ILERISPDSTHDGKSYCLPWIPDFV PKIGLGVITNGFFNFLDDNAVELEQHTSFHGSSLVQGLFHLRSQGNVDTSLCS ISCFQRLLQLSCSID RVIQNATTNCTEHLKESKTGIAGRILEQGICNFWRNNLLDMLTSLLPMI SSQWSILQNIEMFGRGGPA PGVGFGWGAYGGGFWSLNFLLAQLDSHFVLELMKILSTGPEGLVTVNKSVNPIVQEGNNV TDSVAITS ERISSVLSVSLMAGPGQISTLEKAFDILFHPSVLKFLKSSVLDSHMKLAKAFEWDITEDE YLHFSSVL NSHFRSRWLVIKKKHSDEFTRNNNGTNVPKIPETLETIQEETELAEAVNPPCSVLAVEWA HQRLPLPV HWILSAVCCIDDPKANLSTSYAVDVSKAGLFFLLGLEAI SAAPCLHAPLVWKMHALSAS IRSSMDLLL EDRSRDIFHALQELYGLHLDRLCQKYDSAHSVKKEGSASVDEEKVTRTEVLRFQEKIHAN YTTFVESL IEQFAAVSYGDALFGRQVAIYLHRSVEPTIRLAAWNALSNAYVLELLPPLDKCVGDVQGY LEPLEDDE GILESYAKSWTSGALDKAFQRDAMSFTVARHHLSGFVFQCSGSGKVRNKLVKSLIRCYGQ KRHHEDML KGFVLQGIAQDSQRNDEVSRRFEIMKDACEMNSSLLAEVRRLKTSIDR

SEQ ID No. 13 MINIYO Zea mays, GRMZM2G156818_T01 MDATTKRRHQPGGAQPTRRKVVEEPFHTAPPTPAAASPSRLVGAIVEKGYSAAAPSSAPR PSVLPFPV

ARHRSHGPHWVPLVKDAPKDETADNDDEMDMDETDYHPVAAAAAGPVRRKEKKGMDF SRWREFVGDAP PKRRQGKPVQAKKQSDQRIDAGAVASKVGGVAAEGRGLEGGAMRLDSGNASEGPGPVLLV SDVVSKKP MSQVESRDELVNTSEARNLASQAESMDLDGRESSMEAEI SAENMARLAGMSAGEIAEAQADIVNKLNP ALLEMLRRRGREKSGGTKDVGKDKGLKNSGLQKNKRATPGDWLTAGEHTGHSWKVWSERV ERIRSCRF TLDGDILGFQSSHEQQDGKKMPSESVAERDFLRTEGDPAAVGYTINEAVALTRSMVPGQR VLALQLLA

SILNRALQSLHKTDLMDNVKGMNSKDNIDDWQAVWSYALGPEPELVLSLRMALDDNH DSVVLSCTKVV NVMLSCEFNESYFEFSEKVGNGKDICTAPVFRSKPDLDGGFLEGGFWKYNTKPSNILPHC GDNDEDEA DEKHTIQDDVVVSGQDVAAGFVRMGILPRICFLLEMDPSPALEDYLVSVLVALARHSPQS ADAILNCP RLIQSVTKLLINQGSMEIRSSQIRGVTLLKVLSKYNRQTCLNFVNHGVFQQALWHWYRKA GTIEDWVR SGKEKCKLSSAMMVEQLRFWRTCISYGFCIAHFADFFPVLCLWLSRPDFKKLSEHNVLVE FSSVARES

YLVLAALAQRLPLLHSVEQLANQDLGVSASYIETCSWSHVVPMVDLALSWLHLNDIP YVCSLI SEQNR NTEHMLEMSYLILVI SSVLGMLNSILERI SPDVTPEDKSYSLPWIPDFVPKIGLGI I SNGFFSCSTTV AGRNAEHQPFCCASLVQGLCYMRCHGNVDVSLSSI SCLQRLVQLSWSVDRVIQGATKCCSECFNESGT GEAGKLLAEGI SSLWHNDLLHLLTSLLPMISSQWS ISQ IEMFGRGGPAPGVGFGWGTCGGGFWSLKC LLAQLDSQLVVELIKCFSSVQGSPI ILDEGVKLDNVTNTVVTASNWI SSTLGLSLIAGPGQIYMLEKV

FDMIFEPSILKYLKSSIHKFTSDMELLKPFEWDLNEDEYMLFSSVLKSHFRSRWLAI KKKHSDKYAGD NSSTKISKTPEILETIQEETELSEAVNQPCNTLMVEWAHQRLPLPIHWILSAVCCIDDPK GTLSTSAN YILDVSRAGLIFLLGLEAI SATPCLHAPLIWKIHALSVS IRSSMHLLQEDRSRDIFCALQELYGLHLN RLYQKFCKPNS IEEVKGVVVGTSEEAMEI SSLEILRFQEKIHGSYTTFVESLVDQFAAVSYGDFVFGR QVAIYLHRKAEPAVRLAAWNALSSAYVLELLPPLDNCIGNAPGYLEPLEDDEKILESYAK SWTSGVLD KALQRDSMAFTLAKHHLSGFVFQSSDSGTMLRKKLVKSLIRCYAQKRHHEVMLKCFVQQG IAQDSKSS ELDRRFEILKDACEMNSNLVGEVQRLKACLGQ

SEQ ID No: 14 MINIYO Glycine max, Glyma01g08040.1

MTKNENKVDKSVDWEAVWAFALGPEPELVLSLRICLDDNHNSVVLACTKVVQSVLSY DANENYCDMSE IATCDMDICTAPVFRSRPDINDGFLQGGFWKYSAKPSNILPFSDDSMDNETEGKHTIQDD IVVAAQDF TVGLVRMGILPRLRYLLEKDPTTALEECI IS ILIAIARHSPTCANAVLKCERLVQTIVNRFTADNFEL RSSMTKSVKLLKVFARLDQKTCLEFIKKGYFQAMTWNLYQSPSSVDHWLRLGKEKCKLTS ALIVEQMR FWRVCIQYGYCVSYFLEMFPALCFWLNPPSFEKLVENDVLDESTS ISREAYLVLESLAGRLPNLFSKQ CLNNQLPESAGDTEVWSWNYVGPMVDLAIKWIASRSDPEVSKFFEGQKEGRCDFPFRDLS ATPLLWVY AAVTRMLFRVLERMTWGDTISSFETEGHVPWLPEFVPKIGLELIKYWFLGFSASFGAKFG RDSEGESF MKELVYLRQKDDIEMSLASTCCLNGMVKI ITTIDNLILSAKAGICSLPRQEQSLSKEGKVLEDGIVNG CLVELRYMLDAFMFSVSSGWHHIQS IESFGRGGPVPGAGIGWGAPSGGFWSATFLLAQIDAKFLVSLL EIFENASKGVVTEETTFI IQRVNAGLGLCLTAGPREKVVVEKALDLLFHVSVLKNLDLCIHNFLFNRR GRTFGWQHEEEDYMHLRRMLSSHFRSRWLSVKVKSKSVDGSSSSGIKTSPKVGACLETIY EDSDMSSM TSPCCNSLMIEWAHQKLPLPVHFYLSPISTIFHSKRAGTKKVDDVLHDPSYLIEVAKCGL FFVLGVEA MSIFHGTDIPSPVEQVSLTWKLHSLSVNFLVGMEILEQDRSRVTFEALQDLYGELLDKAR LNQSKEVI SNDKKHLEFLRFQTEIHESYSTFLEELVEQFSAVSYGDVIFGRQVSLYLHRYVETSIRLA AWNTLSNA RVLELLPPLEKCFSGAEGYLEPAEDNEAILEAYTKSWVSDALDRAAIRGSVAYTLVVHHL SSFIFHAC PMDKLLLRNRLARSLLRDYAGKQQHEGMLLNLIHHNKPPPSVMGEELNGGVLSERNWLES RLKVLVEA CEGNSSLLIVVEKLKAAVEKSS

SEQ ID No: 15 MINIYO Glyma02gl3360.1

MKVDTKPLLDNSDGGFINSTTTMEVDTLNKEQNESVPGLDQISSDWMPDYNFGSLDV QRPGQTDLNSS MLEQKSVSLDSEIDAENRARIQQMSAEEIAEAQTEIMEKMSPALLKLLQKRGQNKLKKLK LEVDIGSE SVNGHAQSPQDAKHLHTEDGIAQTVIVPPSKEKLDDEKI STKTSTTASSSAWNAWSNRVEAVRELRFS LVGDVVDSERVSVYDNANERDYLRTEGDPGAAGYTIKEAVALTRSVIPGQRTLALHLLSS VLDKALHY ICEDRTGHMTKIENKVDKSVDWEAVWAFALGPEPELVLSLRICLDDNHNSVVLACAKVVQ CVLSYDAN ENYCNISEKIATCDMDICTAPVFRSRPDINDGFLQGGFWKYSAKPSNILPFSDDSMDNET EGKHTIQD DIVVAGQDFTVGLVRMGILPRLRYLLETDPTTALEECI I SVLIAIARHSPTCANAVLKCERLVQTIAN RYTAENFEIRSSMIRSVRLLKVLARSDRKSCLEFIKKGYFQAMTWNLYQSPSS IDHWLRLGKEKCKLT

SALIVEQMRFWRVCIQYGYCVSYFSEMFPALCFWLNPPSFEKLVENNVLDESTSI SREAYLVLESLAG KLPNLFSKQCLNNQLPESAGDTEVWSWNYVGPMVDLAIKWIASRNDPEVSKFFEGQEEGR YDFTFRDL SATPLLWVYAAVTHMLFRVLERMTWGDTIETEGHVPWLPEFVPKIGLEVIKYWFLGFSAS FGAKCGRD SKGESFMKELVYLRQKDDIEMSLASTCCLNGMVKI ITAIDNLIQSAKAS ICSLPCQEQSLSKEGKVLE DGIVKGCWVELRYMLDVFMFSVSSGWHRIQS IESFGRGGLVPGAGIGWGASGGGFWSATVLLAQADAR

FLVYLLEIFENASKGVVTEETTFTIQRVNAGLGLCLTAGPRDKVVVEKTLDFLFHVS VLKHLDLCIQS LLLNRRGKTFGWQHEEEDYMHLSRMLSSHFRSRWLSVKVKSKSVDGSSSSGIKTSPKVGA CLETIYED SDTSSVTTPCCNS IMIEWAHQKLPLPVHFYLSPISTIFHSKRAGTKIVDDVLHDPSNLLEVAKCGLFF VLGVEAMSIFHGTDIPSPVQQVSLTWKLHSLSVNFLVGMEILEQDWSRDIFEALQDLYGE LLDNARLN QSKEVISDDKKHLEFLRFQTEIHESYSTFLEELVEQFSAVSYGDVIFGRQVSLYLHRCVE TSIRLAAW NTLSNSRVLELLPPLEKCFSGAEGYLEPAEDNEAILEAYTNLWVSDALDRAAIRGSVAYT LVVHHLSS FIFHACPTDKLLLRNRLARSLLRDYAGKQQHEGMLLNLIHHNKPPPSVMGEELNGILSEK SWLESRLK VLVEACEGNSS ILTVVDKLKAVVKNSS SEQ ID No: 16 MINIYO Brachypodium distachyon, BD1G37370

MLPMDDGTKRKHQPGAHPTRRKVVEEPFDPAPPLSGAATAAASAAAPPPHLVGAIVE KGFSAAAPSSS PRPTVLPFPVARHRSHGPHWNPVTKDAYKEKGEVEDYGMDVDEVDYQPMATVAGPIRRKE KKGMDFSR WREFMADDVPPKRRQAKKNSTQRIDPGIVAEKVDVSVGERALGGDGMELDGGNAKDELGV TTLVSDVL PRKPEKRVDAGDLLMLEGEAGVAEMRGEGMQLDDGEPSVAAEI AE IARLAEMSTEEIAEAQADILN RLDPTLVEILKRRGKEKSGGRKDGVKDKGGEISEPGKTARATPGARLVVGEHNGYSWKAW SERVERIR LCRFTLNGDILGFQSCQEQQDGKNRNAERVAERDFLRTEGDPAAVGYTINEALALTRSTV PGQRVLGL QLLASVLNRAVHNLHEMDLADNLEGANGADKLDDWQAVWAYALGPQPELVLSLRMALDDN HASVVLTC AKVINVMLTYDMNEAYFEFSEKVVHQGKDICTAPVFRSKPDLDGGFLEGGFWKYNTKPSN ILPHYGEN AEEEGDEEHTIQDDVVVSGQDVAAGLIRMGILPRICSLLEMDPPPILEDYLVSTLVALAR HSPQSADA ILNCTNLVQSVVKLLVKQGSMEIHSSQIRGVTLLKVLSKYNRQTCSNLVNRGVFQQAMWQ WYRKAYTL EDWIRSGKEQCKLSSAMMVEQLRFWRTCI SYGFCIGHFTDFFPVLCLWLSPPLFQNLSKSNVLSEFSS ISRESYLVLGALAQRLPLLHSMEQLGKQDMGVSGSYIEMWSWSHVVPMVDLALSWLHLND IPYLCSLI NEQSENTAHILEESCLVLLISSVLGMLNSILERISPDGTPDVKSYCLPWIPDFVPKIGLG I ITNNFFS FSRDDVVGHEDQLSFCGVSLVQGLCRMRSQGNVDASLSSICCLQRLVQLSFSVDRVIQRV STKCSEPV KESKTGIAGKILGQGISSLWHHDLLNSLNVMLPLSSSQWPVLKNIETFGRGGLAPGVGFG WGTCGGGF WSLKCLLAQLDSQLVLELIKIFSAVPEVLVTPSKGVNSDNVTNPVAKASGRISPVLGVSL IAGPGQIT TLETAFDILFHPS ILKCLKSSMQSMASQMELPKTSEWEITEDEYQHFSSVLNSHFRSRWLVIKKKSDK YARDNSGINMPKLSETLDTIQEEVEFTETVNPPCGTLVVEWAHQRLPLPVHWILSSICCI DDAKGTLS VLANHAVDVSRAGLIFLFGLEAI SSAPCLDAPLVWKIHALSASLRTNMDLLQEDRSRDIFNALQELYG QHLDMLCHKYYRSHSVKNDEVVGSVTTVEEAKAISSLEILGFKEKIHGSYTTFVESVIDQ FAAVSYGD VIFGRQVAIYLHRSVETVVRLAAWNALSNAYVLELLPPLDKCIGDIKGYLEPFEDNEAIL EAYAKSWT SGVLDKASQRDSMSFTLVRHHLSGFVFERNASIKVRNKMVKSLIRCYAQKQHHEAMLQGF VLHGTQSS DEVSRRFEILKDACEMNSSLLAEVHRLKTSIDG

SEQ ID No: 17 MINIYO Sorghum bicolor, Sbl0g022700

MDAPTKRRHQPGGAHPTRRKVVEEPFHPAPPTPAAAAAAAASASPARLVGAIVEKGF SAAAPSSAPRP SVLPFPVARHRSHGPHWGPVAKDAHKDGAADDDDEMDMDETDYHPVAAAAGPVRRKEKKG MDFSRWRE FVGDAPPKRRQGKPVQAKKQSDQRIDAGAVASMVGGVAATGRGLEGGAMQLDSGELEGSA MQLDSGNT REGPGAVLSVSDVVSKKPMSQAESRDELVKVGEVRNSTSQAESMDLDGRESSMEAEINAE NMARLAGM SAGEIAEAQTDIVNKLNPALVEKLRRRGREKSGGTKDVGKDKGLENSGPQKTKRATPGDW LTPGEHSG HSWKAWSERVERIRSCRFTLDGDILGFQFSHEQQDGKKMHSESVAERDFLRTEGDPAAVG YTIKEAVA LTRSMVPGQRVLALQLLAS ILNRALQNLHKTDLMDNVKEMNSNEKFDDWQAIWSYALGPEPELVLSLR MALDDNHDSVVLSCAKVINVMLSCEFNESYFEFSEKVGNGKDICTAPVFRSKPDLDGDFL EGGFWKYN TKPSNILPHYGENDEDEGDDKHTIQDDVVVSGQDVAAGFVRMGILPRICFLLEMDPSPAL EDYLVSVL VALARHSPHSADAILNCPRLIQSVTKLLINQGSMEIRSSQIKGVTLLKVLSKYNRQTCLN FVNHGVFQ

QALWHWYRKAGTIEDWVRSGKEKCKLSSAMMVEQLRFWRTCISYGFCIAHFADFFPV LCLWLSPPEFK KLNEHNVLVEFSS IARESYLVLAALAQRLPLLHSVEQLANQDRGVSASYIETCSWSHVVPMVDLALSW LHLNDIPYVCSLI SGQNRNTKHMVDASYLILVIASVLGMLNSILERI SPNVTPEDKSYSLPWIPDFVP KIGLGI I SNGFFSCLGTVAVRNAEHQSFCSASLVQGLCYMRCHGNVDVSLSSI SCLQRLVQLSWSVDR VIQGAKKSCSECFNESGTGVAGKLLGEGI SSLWHNDLLHLLTSLLPMISSQWS ISQ IEMFGRGGPAP

GVGFGWGACGGGFWSLKCLLAQLDSQLVVELMKCFSSVQGSPVILDEGVKSDNVTNT VVTASNWISSS LGLSLIAGPGQIYMLEKAFDMIFEPSILKYLKSSIHKFASDMVLLKPFEWDINDDEYLLF SSVLNSHF RSRWLAVKKKKHSDKYTGNNSSTKI SKTPETLETIQEETELTEAVNQPCNTLVVEWAHQRLPLPIQWI LSAVCCIDDPKGTLSTSANYILDVSRAGLIFLLGLEAISATPCLHAPLIWKIHALSVSIR SSMHLLQE DRSRDIFCALQELYGQHLNRLCQKFCKSKSVEEVKGVVVATSEEAMEISNHEILRFQEKI HGSYTTFV ESLVDQFAAVSYGDFVFGRQVAIYLHRKVEPAVRLAAWNALSNAYVLELLPPLDKCIGNA QGYLEPLE DDENFLESYAKSWTSGVLDKALQRDSMAFTLVKHHLSGFVFQSSDSGKTLRNKLVKSLIR CYAQKRHH EVMLKSFVLQGIAQDSKSSGNELDRRFEILKDACEMNSSLLGEVQRLRACLGQ SEQ ID No: 18 MINIYO Oryza sativa ssp. japonica , >OS06G37640, Gene

ATGGACGACGCGGCGGAGCGGAGGCGGCGGCAGCAGCAGCAGCAGCAGCCAGGCGCC GCCCACCCCGC GCGCCGCAAGGTCGTGGAGGAGCCCTTCGACCCCTCCCCTCCCCCGGCCGCCGCCGTGGC GCCGCCTT CCTCCCGCCTCGTCGGCGCCATCGTCGAGAAGGGCTTCTCCTCCGGCGCGGCCGCCGCCG CGCCCTCC TCCGCCCCGAGTCCCACCGTCCTCCCCTTCCCCGTCGCCCGCCACCGCTCCCACGGCCCC GTAAGCCG CCTACGCCTCCTCCGCCGCCGCCCTCTATCTCGGAACCCTAGGTTTGATGTGGTGCTTTG GTTTTGTA CTCCCTGACTGACTATCTGCTCTTCCGCAGCACTGGAAACCGGCGGCGAGGGATGCTGCC ATGGCGGA GGGGGAGGGCGAGGAGGAGGAAGGGATGGATGTGGACGAGACGGACTACCAGCCCGTGGC CGCCGCAG CTGGGCCCGTTAAGAGGAAGGAGAAGAAGGGCATGGATTTCAGCAGGTGGCGGGAGTTCG TCGCTGAC GATGCGCCCCCGAAGCGAAGGCAGGCAAAGCCGTTGCAGCCGAAGAAACAGACTGCGCAG AAAATTGA CACCGGGGTCGTGGCTGCAACGACGGGTGGCACCGCACAGGAGAAGCGCTCCGGGGGAAT TGGTATGC AGCTGGAAGTTGGAAATGGTAAGGAAGAATTGGGTGGAGCTGCTTTGATGTCTGATGTGG CGCCAAGG AAGCCGATGAAACAGGTTGATGCTAGAGATGATGTGAGGAATGTGGAATTGCGAGGAGAG GGTATGGA ATCGGATAATGGGGAACCATCTCTTACCGCAGAGATTAATGCGGAGAACATGGCTAGGCT GGCAGGGA TGTCAGCTGGGGAGATTGCAGAGGCACAGGCAGAGATCCTGAATAGGATGGACCCGGCAT TTGTGGAG ATGCTGAAACGACGGGGGAAGGAGAAGTCTGGGAGCAGGAAAGATGGGGGAAAGGGCAAG GGTGGGGG GATTTCAGGCCCAGGGAAGATCTCGAAGGCTATGCCTGGAGAATGGTTGTCAGCTGGTGA GCATAGTG GACACACTTGGAAGGCATGGAGTGAGAGAGTAGAGCGGATCAGGTCTTGTAGGTTCACAT TGGAAGGA GATATTTTGGGGTTTCAATCTTGTCAGGAGCAACAACATGGTAAATCATTTTTCTTTGCT CTTGTGTT GCTTTTAGCTTCTAGTGTTCTGGTACCCGTTACATGTCAACCTGGCTTTCCCACTTACAG GCAAGAAA GCACATGTGGAAACTGTAGGTGAGCGTGATTTTCTTCGAACAGAGGGAGATCCCGCAGCT GTTGGGTA CACAATTAATGAAGCAGTGGCACTTAGCAGGAGCATGGTTTGTTACTTTCTTTTGTTGTT CAGTGTGA AAATGGACTTTTGAGTAAAGTTCAAGGGCTAAAAATGGACTTTACCCAATGCAATACAAC ATCTAGTT TCTCTTTAGTATTTTTAGAGATATTAACCTTTGCATGTGAATGGATTTTGTTGTTTTTTT TTTTAAAT GTCATATCATGCATAACTGAGATACACCATCATCGCTTAATGTTTTTCTTACATCATTTC TAAAGTGT GCCTCCAAAATATTGCAAGATAAATAAATGTAATAATTCAGTTTTTACGTTCAAACCATA GGTTCCTG GACAGCGCGTGCTTGCGCTTCAGCTCCTTGCTTTGATTCTTAATAGGGCCTTGCAGAACC TACATAAG ACGGATCTAATTGATAACTTTAAAGAATCAAATGATGATGACAAGTTTAATGACTGGCAA GCGGTTTG GGCATATGCCATCGGACCTGAACCTGAGTTGGTTCTCTCTCTAAGGTAAACTGGTTGTTT TCAAACTA TAATAATAATTTTAATTTGGATTTGCTTATTCCATGCAAGAGTTTATTAGTTACCAAAGT GAAGAGTA CTTAACTGAAATATACCGGACAATTCTATTAAGACTAAATAATCAAGAAACCTTAACACA TGCTTTAG TGTCTGCACCTATGCTTAAAATTGTATGCCTGAAAATTTGGGCTGCCACATCTTGTATTT TAGTCATG AATTCATGACAGCAGGCAAGCATTAACAGCATAAGGTCATCTTGTCCATTAGCTATCAGT TAGCACTT GTAAGAAGATGTATCCAGTTAACTTAGGCCATGTCTAGTGTAGGTGAAGCTAAGGTTGTC ACATCACA GCCATGTGATACACAGGGTGGATAATTTTTCTTCTCTAGTGTGCTAGCATCGATTTTAGT TTTTGAGT GGACTCCACTAGAAATTTTAAAAACTGGCTTTCCTAGTGTATGCAAATAAAACATTTTGC TTCGCATC

AAACCATATATGCATCGATTTTGTTCCTAGCATCTCCTCTTCTAGTGCCTAGAATCA TTACTAAGCCT TCAAATCCGCTTGCTAGCATCGGTCAAGGTGTGCACTAGACATGCCCTTATTGTCTTTCT TTTTGCAG TCACGTTGGCTGTTTCATGTATAATAAGTTAGGAAAATTCCATCTATAGCACAAAGTTTT CATAGGTA CTAATAAATACCACAATTTTCAACCCTTCCAGAAATGCCACAATGTGACACCACACGTAA AAAATACC ACAAAATTTTACAGAACTGAACGTATGACAAATTGAACTATTACCATGGACAAAATTGCC CCTGGCCT

TTCTTCAATCTGCATTCAGTAGTCTCCCCGTGATTCCACTCGTCTCCTCTCTCTCTC TCTCTCTCTCT CTCTCTCTCTCTCTCTCTCTCGGCGAGATGAAGTGAAGCTGGTGGCCACGAATTCCGGCA ATGAAGCA CGGTCCTACCTACAATCCGTCCTCGAGGACTAGCGACCGCCGCCAGCCGCGGAGGCCGCC AGCGCCGA GGCCGCTGAGGCGTTGGCTCTCGAGGTGAAGTCTTCCGCACTCCTCCCGTAACCGATGAA GGTCTGGC AACCATGGCCATGCCTCTGACCTGCTCTAGCGTGATCCAATCACTTGGTCTCACAGGTCT CCATGATG

CTCTTATTGCCGGCGGCCATTGCAACATCCACACATGCATCCGAATCATATGTCCCC AAATCCGAACG CCTAAATCCATTTCCTCCTTGTGTTATTCTCTTGGCCACAGAAAACACCTCGTTTTGGCA GGATTTGC TGCGAATCAAGCCAAATAATCCATTGCCTTCGTGGTAATCTGGGCATTTTCTTTGTAAAA TGGCACTG TCCATCCCCGCCTTGTTCTGTTCTGAGTTGTGGTATTTCTGAAAGGGTGGAAAAATCCAT GGTATTAT TAGGTACCAGTGAAAACTTTGTGCTATAGATGGAATTTTCCCTAATAAGTTATAATCTCA GAAAACTG

CGGTGTGACCTAATTAACTGTTGTCTATAGGTTTTTTTTATTTAGTTCTCTCATATG CCATCTAATTA GTTTCTTTGCTTATATGAGTTAATTGCACCAGTGTTAGACCTTAAAATGGCCTATGCTTT TTTCATTG TTTATTCTACTTATGTGTCATCACTAACTGGAATATCTGCAGGATGTCATTGGATGATAA CCATGATT CTGTAGTTTTGACTTGTGCTAAAGTTATCAATGCTATGCTGAGCTATGAAATGAATGAGA TGTATTTC GATGTTTTAGAGGTAACTTTACTAATTTATCTTCTAATTTGTTTTTCGTTGAGAACTTTA TCCTTAAA TGGCTGATTTTCAACATTACAGAAAGTAGTAGATCAAGGGAAGGATATCTGTACAGCTCC TGTTTTCC GTAGCAAACCTGATCAGAATGGGGGTTTTCTTGAAGGAGGTTTCTGGAAATACAACACAA AACCATCC AATATACTCCCACATTATGGTGAGAATGATGAGGAAGAAGGTGATGAGAAACATACCATT CAAGATGA TGTGGTTGTATCAGGTCAAGATGTTGCTGCTGGTCTTGTTAGAATGGGAATACTTCCACG GATCTGCT TCCTTTTGGAGGTGAGGGTCTGGCCATCTGCTCTCCCTCATCCCCTATCTGCCATTGTTT CTTTCAGA

ATCCCACTGCCATGCATGCACCCAGAATCCCACCGCCATGCATGCACAATATGGGTG CATTAGGTCAT CTTTTGTTTACTATATCCGTGAATTGTCTGGTTCCTTGATGTTCAATCCTGTCTAGTACT TGCCATCC ATCCTTGAAATGGCAGTGAAATGCCTCCTTACCTGGTTGACACATCACTTGTTTTCACCA GGAAATCT GGTTTGCAGCAGAATTTGTGGCTGGCTTTGATTGTTCTTTTACCATCGGAAAATTACAAT TTTGATAT TCAACAACCAAACTATGATAAATTGTGTATAGCCTTTCATTTTTAGCAATATTTTTTATT TCCTGAAG CTATGGGCCTTATCCATTTGCAGTTTTAAGTATTTTGTAGTTCTATGATGTCATGTCATC TGATACCC GTAATCTTTCAAACTTCTTATCTGGTTATTGGACTGTCTCGTAGATTGTTCTGTTCACCC TTGGTGCT CTTGCTTGTTGACTGTTTGTTTTATAGTGATAGCTTTATATTGCAGTTCTATTACTTCAC TAGTAAAC ATCATTTGAGCTAGTTGGTCTTCTTTTTATTTATGTTTTCATTTCCTATTCTACGAGAAA GTGATGGT CATGATTACGGATCTTAATGGTCAAGTTTTTGTTGATTCAGATGGACCCACATCCAATTC TAGAAGAT AATCTTGTTTCAATTCTTTTGGGATTAGCGAGACACTCTCCACAATCTGCTGATGCTATC TTGAACTG CCCAAGGCTCGTTCAAAGTGTTGTTAAGTTGTTAGTCAAGCAAGGATCAATGGAAATTCA CTCCTCGC AAATTAAAGGAGTCAATCTCTTGAAGGTATCTTCTGGTGATATAAATAATCTTTTATTAT AGGAGTAT GCTGATTTTGTGTAGTTTTGGAAGTTGCAGATTATTTATTATATAGTTTTTCTTCTATAT CATTGGTT GATAATAACTTGATCTAGTTATCCTTCAGAAGGATTCCTTCTGAAGGATAACTAGATCAA GTCTGCCA GTAATACCACTTGCAATTGCTGATTGTACATCTGAAATGGTTTCCTTTTGTTGGTAATTA GCTACCAA CAGCATCATTATGAGTTTTTTTTTTGTTTGCTGCTTCTGATATCTTAACACATAGCAATT GTATTAGC CATGCCTGCTGTTATCTGAATCAATCACACTCCTTGCACAATGCCTTCACTGTCAACACA CAACTGTT TGGTCCCCCCCCCTCCTGCGGGCACTTTAGTTGCCCCATTAATTCATTATTATGGTAAGA TGAGAAAC ACCATAGTCATAAGATTTGAATGTTCAGATTATGCTAAAAAAAATCATTACTTCTATTTC TAAATTTG TCAAAGATTTTTTTTTCACTAGCATCTAATTTCTTGTTCCTTTTGCCTAGGTTTTGTCCA AGTACAAC AGGCAAACATGCTTCAATTTTGTGAACACTGGAGTTTTTCATCAGGCTATGTGGCACTGG TACAGAAA AGCCTATACTCTTGAGGATTGGATAAGATCTGGAAAGGAGCACTGCAAGCTTACTTCAGC ATTAATGG TTGAGCAGCTGCGGTTTTGGAGGACCTGTATCTCTTACGGGTTTTGTATAACGCATTTCA CAGATTTC TTTCCTATTTTATGCCTGTGGCTTAGCCCTTCGATGTTTCAGAAGCTAAGTGAAAGCAAT GTTGTAGC TGAATTTAGTTCCATTGCAACAGAGAGTTATCTTGTATTAGGAGCTCTGGCTCAAAGGCT TCCACTTC TTCATTCAGTTGAGCAGCTTAGCAAGCAAGACATGGGACTTTCTGGTATCCAAGTTGAGA CATGGTCG TGGAGCCATGCAGTTCCAATGGTAGATTTGGCGCTATCTTGGCTATGCCTGAATGATATT CCTTATGT GTGTTTGCTAATCAGTGGGCAAAGTAAGAATATACTAGAGGGAAGCTACTTTGCTTTGGT TATTTCTT CTGTGCTAGGCATGCTTGATTCAATACTAGAAAGGATATCTCCAGATAGTACACATGATG GTAAAAGT

TACTGCTTGCCTTGGATACCTGACTTTGTACCCAAAATTGGCCTGGGAGTTATTACT AATGGATTTTT CAACTTCTTGGATGATAATGCCGTTGAACTTGAGCAACATACATCTTTCCATGGTTCATC GTTGGTGC AGGGACTTTTTCATTTGAGATCCCAGGGTAATGTTGACACATCATTGTGTTCAATTAGTT GCTTCCAA AGGTTATTGCAGCTATCTTGCTCTATTGACAGAGTAATCCAGAACGCCACAACAAATTGT ACAGAGCA TCTGAAAGAATCAAAAACAGGGATAGCTGGCAGGATACTAGAACAAGGTATTTGCAATTT CTGGCGTA

ATAACTTGTTGGACATGCTAACTTCATTGTTGCCAATGATTTCCTCACAGTGGTCCA TATTACAAAAC ATAGAGATGTTTGGTAGAGGAGGACCAGCACCTGGTGTTGGTTTTGGTTGGGGAGCATAT GGTGGAGG ATTTTGGTCTTTGAATTTCCTTCTTGCACAATTGGATTCACATTTTGTTCTAGAATTGAT GAAAATCT TGTCCACGGGGCCAGAAGGCCTTGTCACCGTCAATAAAAGTGTGAATCCAATTGTGCAAG AAGGAAAT AATGTGACTGATTCAGTTGCCATCACTTCAGAGAGAATCAGTTCTGTCCTCAGTGTATCT TTGATGGC

AGGACCTGGGCAGATATCTACACTAGAGAAAGCCTTTGATATCCTCTTCCACCCTTC TGTTCTGAAGT TTCTCAAATCTTCAGTACTAGACTCACACATGAAATTAGCAAAAGCTTTTGAATGGGACA TAACTGAA GATGAGTATCTCCATTTTAGCAGTGTACTGAATTCACATTTCAGATCCAGATGGTTGGTC ATCAAGAA GAAGCATTCAGATGAATTTACAAGAAATAACAATGGCACAAATGTGCCAAAAATACCAGA GACATTGG AGACGATTCAAGAAGAAACAGAGTTAGCAGAAGCTGTAAATCCACCTTGCAGTGTGTTAG CTGTAGAG

TGGGCACACCAGAGATTGCCCCTTCCTGTGCACTGGATTCTAAGTGCAGTCTGTTGC ATTGATGATCC AAAAGCCAACCTATCAACCAGTTATGCTGTTGATGTTTCAAAAGCTGGTCTCTTCTTTCT TTTAGGTC TGGAAGCCATTTCAGCGGCTCCATGTCTTCATGCTCCTTTGGTTTGGAAGATGCATGCAC TTTCTGCC TCTATCCGCAGTAGCATGGATTTGCTTCTAGAAGACAGAAGTAGGGATATTTTTCATGCT TTGCAAGA ACTGTATGGCCTGCATTTGGATAGATTATGCCAGAAATATGACAGTGCTCACTCTGTCAA GAAAGAAG GATCAGCCTCTGTGGACGAAGAAAAGGTGACCAGGACTGAAGTTCTCAGATTTCAGGAGA AAATCCAT GCAAACTATACTACTTTTGTTGAGAGCCTTATTGAGCAATTTGCAGCTGTCTCATATGGT GATGCTCT TTTTGGTCGACAAGTAGCCATTTATTTGCACCGGAGTGTTGAACCCACAATTCGGCTTGC GGCCTGGA ACGCTCTGTCTAATGCTTATGTGCTTGAACTGTTACCTCCACTAGACAAATGCGTCGGTG ATGTTCAA GGGTACTTGGAGCCTCTTGAGGTATTGTCTCTTTAGTTTCTTGTATGCTTGTCTTTTGGT TGGCATTT

TGTAGTAACAATGTAAATTTGGGTCTAGAAGTTTGCTTTATACTACTGCTTTTGGGG TTGCACATTAC ATAGAGTATGCAAAGAGTAAACAATGCATGCTATTTTTCTTAACTATTTGATTTCGGTAC ATACATGA GCACATGCCATGATTCTTTGTAAGCATGTTCCCACCTGCTTGTACTTTGTTGCATCTGTG TGATAAAA CAGTTTCAGATTTTCTGATTATTATTTTCACAATAATTTTGTAGGATGACGAAGGAATTT TGGAGTCT TATGCTAAATCATGGACTTCTGGTGCCCTTGACAAAGCTTTTCAGCGGGATGCAATGTCT TTCACAGT AGCAAGGCATCACCTTTCTGGCTTCGTCTTCCAGTGCAGCGGTTCTGGCAAAGTGCGGAA TAAGCTGG TTAAATCGCTTATCCGGTGCTATGGCCAGAAGCGCCATCACGAGGTAATTCCCTCGTGCT TTCCGGAA TATTAGTCATATATTTCATAAATCATGAACCATCCTTGATGTTTGGAAAATTCTATACCG CAGGATAT GCTCAAGGGTTTTGTTCTACAAGGCATTGCGCAAGATTCACAACGTAATGATGAAGTTAG CCGACGAT TTGAAATCATGAAGGATGCTTGTGAGATGAATTCTTCTCTTTTAGCTGAGGTTCGGAGAC TGAAGACA TCAATTGATAGATAAATGGCCCCAAAAGCATTTCACATGCACTCAGAGAAGGAGCAATTT TTTTGGTG ATTGTAAATAGTAACATGTGTCAATGACAAATGGCTAGAGAATAGTTGCATTGTTCGAGT TTACTTTG CATTACAAACCAACCAAAGGAAAACATCAGTGTGTGTAGGAGTGCTCCCGGTTGTGGCTT GTGGGTTA CATTTTAAAGGACAATGAAACAGACTGGTGTTACAGAGATGCTAACTCCAACCTTATGCT CCAGTATC CAACATTTTCTCC

SEQ ID No: 19 MINIYO Zea mays , >GRMZM2G156818, Gene

ATGGACGCGACGACGAAGCGGCGGCACCAGCCCGGCGGCGCGCAGCCCACACGCCGT AAGGTCGTGGA GGAACCCTTCCACACCGCACCCCCTACACCTGCCGCGGCGTCCCCCTCCCGCCTCGTCGG CGCCATCG TCGAGAAGGGCTACTCCGCCGCCGCACCCTCCTCGGCGCCCCGACCTTCCGTCCTCCCCT TCCCCGTC GCCCGCCACCGCTCCCACGGCCCCGTAAGCAGACGCCGCCCTCCCAAACAAACCCTAGGC TCCTAACC CGCTAACCTCGATTTGCTTCGCCGCTGACCAACTACTACTTCCCGTTTCGCAGCACTGGG TTCCCTTG GTGAAGGACGCCCCCAAGGATGAGACCGCGGACAACGACGACGAGATGGACATGGATGAG ACAGACTA CCATCCTGTGGCAGCTGCTGCAGCTGGTCCTGTGAGGAGGAAGGAGAAGAAGGGCATGGA TTTTAGCC GGTGGCGTGAGTTTGTTGGCGATGCTCCCCCCAAGCGGAGGCAGGGGAAGCCAGTGCAGG CCAAGAAA CAGAGCGATCAGAGAATTGATGCTGGGGCTGTAGCTTCTAAGGTAGGTGGTGTGGCAGCT GAGGGGAG AGGATTGGAGGGAGGTGCTATGCGGCTTGACAGTGGAAATGCTAGCGAAGGGCCAGGTCC CGTGCTTT TGGTTTCTGATGTCGTGTCCAAGAAGCCAATGAGTCAGGTTGAATCGAGAGATGAATTGG TGAACACA AGTGAGGCTAGGAATTTGGCATCACAAGCAGAGAGTATGGACCTCGACGGCAGGGAGTCA TCTATGGA

AGCAGAGATCAGCGCAGAGAACATGGCTAGGTTGGCTGGGATGTCTGCAGGGGAGAT TGCAGAGGCCC AAGCAGATATTGTAAATAAGCTGAACCCTGCATTGCTGGAGATGCTGAGGCGGCGGGGAA GGGAGAAG TCTGGAGGCACGAAGGATGTGGGTAAGGACAAGGGTCTGAAAAACTCAGGGCTGCAGAAG AATAAAAG GGCTACACCAGGGGATTGGTTGACTGCTGGTGAACATACTGGGCACTCCTGGAAGGTGTG GAGCGAAA GAGTGGAGCGGATCAGGTCTTGTAGGTTCACATTAGATGGAGACATATTGGGGTTCCAAT CTTCTCAC

GAGCAACAAGATGGTATACCACATGGTTTTGCTCATATGAGCTACATTTGCTTCTGT TGGTGTGGTAT CCTTTAGATGACAACCTATATCTCCCACTTTCAGGCAAGAAGATGCCTTCAGAAAGTGTT GCTGAGCG TGATTTCCTTAGAACAGAAGGTGATCCTGCAGCTGTTGGGTACACAATCAATGAGGCAGT GGCACTTA CCAGGAGCATGGTTTGTTTTTTTTATACACCCTCCATTTCGAATTTTATTTGTCCATTTA CTTGGGAA TTGATTTTCCTGTCGAATACGAATGAGAGCTGTTTCATTGCATTTAGAAGAAAAACCAGA ATACAATG

CACCCACAATATGTGCCACATCCACACACCAATCTCTTAGTTACAATCGCTTCAGTT ACATAAAGAAC ATGAGCCGACCTGAACACTATCAAGACAACTATGAGAAAGTTGTTGAAGTGTATAAGTGG ATTGGCTA CCTTCTCCCATCAGCTTAAGCTTTTGGGTTGAACTGGTTAGTGCGTCCATTCTAACATGG TATCAAAG CCAGAGGTCTCGAGTTCGAATCCTGGCAGAGGCTTTATTTGTGCCTCCACCCATTTATTT CCACGTTT GCGCCTTTCTCTCTGGCTGCGTTCGCGCCTTTCTCTCTGGCTGCACGTGAGTGGGGGTGT TGAAGTGT

ATAAGTGGATTGGCTACCTTCTCCCATCAGCTTAAGCTTTTGGGTTGAACTGGTTAG TGCGTCCATTC TAACAAAAGTAACCAGGCAATGCGTTCAACCTGCCTTAGCCCTTAGCAGCAGCTGCATTG CATATATT TATATGGGCACATGGCCATTGTTACAGACTAGGAGTTGACCATTTAGGGATGAAAATGGA TACTTATT CGGATATCAATTTTTTGATCTTTTTTCTTTGATTGTGAATAAATAGGATATAAAATCTGT TATGTAAA TTCATATTCTTGTTTTTAGCATTGAGCTTGTAAAGTTACATAAAATCTTAAAAAGTAAAC CTCAAATT TATCATATATCTTCTCAAGTGATAGATATAAAATTTGGATACAATTCAGATTTGGACACC AATAATTT TTTTTACCTTTTTTGTTGTAGAGAGCAAATAATGTATAAAACAGTTCATGCAAAATTTTA TTCTTATC TGTAATAATGTGCTTGATAACACAAAAAAAGATTAACATCAAGGTGCTAGGCGAGGTAAT GAGTTTTT TTCCCACAAATTTGGTTTGTATAGAGCGTTAGCTATTGAATTGGCTATATGGCAAGTTCA ATATTCTA GTCTATTTTATACGTATTTGGTGAAGGTAGTAAATAGTAACCGTTTTTTCTCGAACGCGC AAGAAAAA

TGCACATCATTAATTCATTATATTAAGAAGATGTAGAAAAAGGTCCATGAGGACCAG TACAAAGTCAG GCACCCCTTACGGTGGCCAAAAACAGGAATACACAAAAGAATCCACAAACATTCTAGCAA ACGAAACT CTACTCAAGACCAGGGATTGGGGCTGTTAGGAGGTCAGAGGAGTATCCGAGGAAGACACA GTGAGTGG AGCGGGGGGCTAGTTTATGAGGAGCAGTGGAGGCGAGATTAGGGTAGCAAGCGCACCCGA AAACACAA AGATGGTTATAGGAGGGGTGGATGCCGAAAAGAGCGAAGTAAGGAGTGGGGTGGGTAACC GCCTTGGT GGGAAGACAGTTGAGGAGGTAGGTGGCAGTGGCGAGGGCCTCAGCCCAGTAGTGAGCAGG AAGGGAAG CCTGAAAGAGTAGAGAGCGCACAACATCGTTCGTCGTGCGAATCATACGTTCAGCCCTGC TGTTTTGA GGAGACGTGTAGGGGCATGACATGCAGAGGTGGATGCCGCGAGAGAGGAAGAAGTCACGG GACACATT GTTATAGAACTCACGCTCGTTGTCACACTGGATGCTCCGGATGGTGCGACCGAACTGAGT AGAGACCC AGGCGAAGAAGTGAGACAGGGTGGGAAAAGTGTCCGACTTCTGACGTAAAGGAAAAGTCC ACAAATAA TGCTAGAAGTCATCGAGAATGAGTAAATAATACTCATAGCCAGAAATGCTGGTTACATGG GATGTCAA TACATCACAGTGTATCAGATCAAAAATGCCTGCTGCTCTAGAGGAGGAGGTGGGGAATGG GAGCCTAA CATGGTGACCTAACTGACAAGCATGATAGAGGTGCTCAAAAGATCCCCTACAACCAGAAA CAGAAGTA CTACTGGAGAGCTTGGACATCACATCACGCCCGGGGTGGCCAAGACGACGATGCCAAGTC GCAGAAGA GGCGGTCGCTGCAAGAACATGTGGGGCAGAGGTCGAAGTAGTGGGAGCAGGTAGACGAAG CGTGTAGA GGGGCCCGGGGCTGTCACACCGAGCGAGAAGAGTCCTGGTGGCAAGATCCTTCACAGAAA GACCAAAC GGGTCAAACTCCATGGGACAAGAGTTGTCAGTAGTGAACTGACGTACGAAAAGAAGATTT TGAATGAT GTGGGGGGCAACAAGGACGTTGGTTAAGCGGAAAGGACCGGGAAGGACCGCGTCACCTAC TGAGGTGA CGGGAAGGGCGGACCCGTTTCCGACAATGATGGAAGAGGGAAGAGAAGGGTGGACGGGGG AGGTGGAA GATAGAATACATGCGTCCGGGGTGGTGTGGTAGGAGGCGCCGGAATCCGCCACCCAGTCA GAGACTGA GGTGGGCGGGGCCAGCGTCATCATGGAGAAGGAGCTGGCGAGGGATTGCGCGTCCCACCC GTTAGTCC AAGGCCCCCACATGGACTGAGCCGGAGACCCCGGGAGTGGCAGAAGACCTTGCTGAGGCT GGGGAGGA GCCGAGGGTGCCGCCGGGGGTGCGGCGGCAAAGAAGAACTGCTGAGAGGCGGTGGGGCAA GGGGCCGA GGCACCCGTGGACCGCCCGAGCCACATGTGAATGGTGCCAGTCCACGGGTTGTAGAAGGA TGGCCACT GAGAGCCGCCCGAGGAACCACCACGGCCTCCCGACGGGCCATCGCCACTGCGTCCGCCCT TGCGACCA CGGCCGCGACCGCGGCTGCGAGCCCCCCCGAAGCCAGCAGTCTGTCGCGAAGCTCCAGAG GGCAGCGG GGCTGGAGTGCGGGGAGCAGGAACCCCCCCCGGAGTCGGAGGGGGCAGCCTGAGGTGCGC TGTAGAGG GCCGTGGCGGGAGCGGTGGTTGCAGCGGCGGAGAGGCGAAGCTCCTCGAGAAGCAGATCG TTCTTAGC

CTCCGCAAAGGTGGGAAACGGCTTCATGCGGGTGAGGATGGGGGCCACGCGATCGAA GCGAGTACTCA GACCACAGAGGAGGTTGAGCACGAGGCTCTCATCGGTCATGGGAGCCCCGAGGGTGCGGA GAGTGTCT GCCATCGTCTTCATCTGACGGCAGTACTCGTCCATAGAGAGATCGCCCTGAACAAGCTGG CGGAAGGC GGTCTCTAGGTACAGGATCCGAGTCTGGCGGTTGTCGAGGAACTGAGCCTCAAGGGCACC CCAGATAC GGTGAGCAGTATCGTCCGGCACTCGAACAATGTCTTGAAGTTCGGCGGTGAGGGTGCCAT GGATCCAA

GAGAGCACCACTTCGTCCATCAGGAGCCAATCTTCCGTCGGTGCAGCGACCGTGGGG AGGACGTGGTC GGCGAGGGCGTAGCGGCGGAGGGTCTGCAGGACCTGGTCGCGCCACCGAGGATACTGAGT GGAGTCCG GCGCGAGAACGTCGGTGACGGTTGCCCGGATGCTGGTGAGGGCCGCCGCCTGGGCGTGAA GAGAGGCG CGAAGGGTCGAGGTTGGGACGGGCGCGGGCTCGAAAGTGTCGGCGCTGTGACGAGCGGAC ATGGGAGA ACCATCTGAGACGCCCTTGCCAGCGAGGCGACGATAGGTCTCGGCGTACTGGCGCTCGAT GGCGTCGA

CAACCGCCTGTTCCTGCTCAAGGGCACGAGCGGCGTCCTGGGCCCACTGGCGAGCCG CCGCAACGGCA GCACGGGTGGCAGCGAGGATGGCTGCAGCGTCATCCGAAGGGGAAGGAGCACGCAGTGTA GAGGTGAT AGCGGACGCCTGGCTATAGACCGTCGTGCCAATGGTGCCACTGGAAAAAACCAGGGGCAA CAACACGG CGTCGTCGTGGCCGAGCACGGTGGTCTGGGACGCGTGAGGAAGGGAGATCGGCGCGGGAC AGACACCG GCAAAGCCGGAGCCGGCCGGACTCGGCAGCGGCACGGGCGAAGGAAGCGCCGGCGGCGCA GGGGGCGC

AGGAGGAGGGGCAGCGAGGCCGGGGGCGGGCAGACCCGGCGGCAGAGGTGTGGCCGA CACGGGCTGTG CGCCGGCGGGGCCGGAGCCGGAGTCGCTGGAGGGCGGTGGCGGCGCGGGGCTCCCGGCCA TGAGGGCC AGCCCGGCGGGTGGTGGCGCGGCCGACGCGGGCCCGATCCAGCGGAGGGAGGCCGGCGGC ACGGGATG CCCGGCCAGAGTCGCGCCGCGCGCGGGAGGAGAGGGCGCGGCCAACGCAGCCCTGTAGGA GAGAGGGA GAGGAGGGAAGAGCTCGCCGGAGGAGGGGAGAGGGGGCCGGCCAGCCATGGGGCGGCGGC TGGAGGAA GGGAGGGGTGGCGGCGGCGGCTGGAACAGTCAAGGCTCTGGTACCATGTGGGAATGTCTG CTGTTACA GAAACCCTGGCTACAGTGCGGCTGCGGCTACAGTACTAGTAAACCCTAGCTACAGTATTA GTGACCTA ATGGGCCAGGCCCATGTACATATATCTGTAACAAGTTCTATTGTTCCTTATTCTCTTGGG TACTACAG CAAAAAGTCTAGGAGCAAGATCCTCAATCCTTTTTCTTTGAAGCCAGCGGTCAGTCCAGA ACAAGGTT GAGGAGCCATTACCAATTTCAGTGATTACAGCAATGGAAAAGAATGCTTTCACTGTTTCA GGGAGCTG

CATAGGGAACAAGATCCAGGGTTTTGAAGGATCAGTTTTTGCTAACCACAGCCATCT CACTCTTAGAG CCCAGCCAAGTTCTTTTTGGGTTTCAAAGAATACATTTTTACCATCATCTGTTAAAATGT ACTTCTAA ATTTTTAGAAGTTGCAATATCATGACATATGATATAATTCAGCTTCCTCAAATTATAGGT TCCGGGGC AGCGTGTGCTTGCACTGCAACTTCTTGCTTCTATTCTGAATAGGGCATTGCAGAGCCTTC ATAAGACC GATCTAATGGATAATGTTAAAGGAATGAATTCCAAGGATAACATTGATGACTGGCAAGCA GTTTGGTC CTATGCCCTTGGGCCTGAACCAGAATTGGTACTCTCCCTAAGGTAAATTTACCTTTCTTA AATACCCC TTTTATTATCAATGCAAACCCATTTTCTTGGGAGTTAGCTTCACAATTTTATCTACTGAG GAAGTGAG TGGAGCTATTGCATGGTTTCTACTCTTTACCGATATCTAGTGCTGACACTGGCATTCTAT CTACTGAG TGTTTGTGCTATGTGAGTTTGTGATCTAAACGTCATTTTTTATTTATTGGATTTAGTGCT TCCTTGTT ACATGCACGGAGTAATATTATGCATTCAGATTTACAATGCATATAAATGAAGAGAACCAT AAATGGAA CATTTGAATAGTTTTGATCAGTAGTAAACATGTAAATACATTCATGGACCTCTCATATTT GTGTTGTC CCTTAGCTGTGTATTTTAAATTTAAAGGTGGCATGTGTGTTGGTGTTTGTGTGTGCATCC ACCTTGTA ATCTAAAATACATGGTTGCATTTTTTTTGTTTGACCCAAAGACAACTACTTGGATTTGAG ACCTTGTG ATGCCATTTTCTTTTCTTTCCTATTTTCTACTCTGCACTCTGTCACTAACTGATGCATTT GCAGGATG GCTTTGGATGATAACCATGATTCTGTAGTTTTGAGTTGTACTAAAGTAGTTAATGTTATG CTGAGCTG TGAGTTCAATGAATCCTATTTTGAATTTTCAGAGGTAATTTTGTCCTTTTTGGGCAGTTC TAGTCTAT TTTCGTTGCTAGTTTGAGCCTCATTTTGTCATTGTTATACCTGCAGAAAGTAGGTAATGG AAAAGATA TCTGCACAGCTCCTGTGTTTCGTAGCAAACCTGACTTAGATGGAGGCTTTCTTGAAGGTG GGTTCTGG AAATACAACACAAAACCTTCAAATATACTCCCACATTGTGGTGATAATGACGAAGACGAA GCTGATGA GAAGCATACAATTCAGGATGATGTTGTTGTGTCTGGCCAAGATGTTGCTGCTGGTTTTGT TAGGATGG GAATACTTCCACGAATCTGTTTTCTGTTGGAGGTCAGTTTGCCTTATTCTTTGATTTGTT GTCGTTTC TTTGAAAATACTTCAAACATGCGGAAGTTACATTGACTTTTGTGGTTTCTTATGTTCAAT AATACATA ACCCACTCGATGTTATTTGCACTTACTCATGCCCCCACACTATTGAGTGATGTCAGGGGT GGTTTGAA AGTTTGACTAATTTTTAATGGCCAATGCCGCTATTGGGCCACCTGGTCCTCACCAGCAAA TATCATTT TGGTCACACCATGTCAATATTTGTTGCTAGTGAAAGTGTAATAAGATAATTATGATTAAC TTTTGAAT TTTTAGCACCAACCTTGGGAATTGGGAAATTTTAGAACATATTGTGGTGCTAGGTGTCCT ATAATTAT GACTCCGTTATCAATTACTCACTCGTGTACAGCTTTGTTGTTGTTGCTTGCCCCATCCTG TGGGGCTA GTATCTAGGGCATTTCTATTCCTCTTAATTTATGCTCGGATCCCCTACTATTTTTCTTTT GAAAAATA ATTGCCATATAATTTTAACTGGATGTACCTATTAATTTATTATATCTTTTATCCAACATC TGCATATA ATTTTGAATGTATACCCTGGCTTGTGTGCTGTTCTCTTGAACTGTCTTGATATTTGTTCC ACTATGTA

TTTTGTAGTGATAACTGATAACGGTGCACTGCACTTGTACATTTCTAGTGAGCCCTG TATCAGCTAAT GACTAGTTGACTCATTTTTTTGCTAATATTTTTGTTCTTTTCATTCAAAAAACTGTATTC ATTATGGG TGTTAAACTGAACCTTTTCTTTTCCATTGGTTCAGATGGATCCATCTCCTGCTTTAGAAG ATTATCTT GTATCGGTTCTTGTAGCACTAGCCAGGCACTCCCCACAATCTGCTGATGCAATCTTGAAT TGTCCAAG ACTTATTCAAAGTGTTACTAAGCTGTTGATAAATCAAGGATCAATGGAAATTCGCTCCTC ACAGATCA

GAGGGGTTACTCTCTTGAAGGTATTTTTTTGGTTCTTTTGACACCCCCCGTGTTATA GAGTTATCATG ATAGATAGTTGGAATCATCGATTGACATATATTGCACACATGTTGATAGTTTGATGCTGA ATAATTCC TGTACGTGCAGATTATTATTAGACAGATGCTTCTCTTGGTCATCCTTGCTATTTTACTGA CCGGGAGA TGTTTTAATATTCCCAGTAATGTGTGGTACTCCGTACTCGTCTGAATTATTAGTTGAGCT CAAATGAT TTTCTTTGTATGCAAGTGCATTAATAGTTCACATTGAATTGCCATATGATATACATGTTC CATGAATC

GGTTCCTTTCTAGTTCAGGATGCTTGCTCCTTGTCTCCCTCAATCACACTGTTCTCC ACATTTTATGT ACCCACACATACTAATTATGTGTTTTGATATTTTATAGTCTACATATTCACTTATATGTT CCAGTATT ATTATTATTTGAAAATACAAGCATCTTGAAAGCTACTGCAATTGAGTCATATTCCAGAAA ACATGTGC AATTTTCTTTGTTTTTCTGCCAAGCAGGACTTCTTTTGACCATCTAAAGCCACCTATTCT GTTTTGAT CAGGTTTTGTCCAAATACAACAGACAAACCTGCTTGAATTTTGTGAATCATGGAGTTTTC CAGCAGGC

ATTGTGGCACTGGTACAGAAAAGCTGGTACTATTGAGGACTGGGTAAGATCTGGAAA GGAAAAATGCA AGCTTAGTTCAGCAATGATGGTTGAGCAGCTGCGGTTTTGGAGAACCTGCATCTCCTATG GGTTTTGT ATAGCTCACTTTGCTGATTTCTTTCCTGTTTTGTGTCTGTGGCTTAGTCGTCCTGATTTT AAGAAACT AAGTGAACACAATGTTCTTGTTGAGTTTAGTTCCGTTGCTAGAGAGTCATATCTTGTCTT AGCTGCTC TGGCACAAAGGTTACCACTTCTTCATTCAGTGGAGCAGCTTGCCAATCAAGATCTGGGAG TTTCTGCC AGTTATATTGAGACATGTTCTTGGAGCCATGTTGTCCCGATGGTTGACTTAGCTTTATCT TGGTTACA TCTTAATGATATTCCCTATGTATGTTCACTAATCAGCGAGCAGAATAGGAATACAGAGCA CATGTTAG AGATGAGTTATCTGATTTTGGTGATTTCTTCTGTGCTAGGCATGCTTAATTCAATTTTGG AAAGAATA TCACCAGATGTCACTCCTGAGGATAAAAGTTACAGCTTGCCCTGGATACCTGATTTTGTC CCCAAAAT TGGCCTGGGCATAATTAGTAATGGTTTTTTCAGCTGTTCGACCACTGTTGCTGGTAGAAA TGCAGAAC

ATCAGCCTTTTTGCTGTGCATCTTTGGTGCAGGGACTTTGTTATATGAGATGCCATG GTAATGTTGAT GTATCATTGTCTTCCATTAGCTGCCTTCAAAGATTGGTGCAGCTATCCTGGTCTGTCGAC AGAGTGAT CCAGGGAGCCACAAAATGTTGTTCCGAGTGTTTCAATGAGTCTGGAACAGGTGAAGCTGG CAAACTAC TAGCTGAAGGTATCTCCAGTTTATGGCATAATGATTTGCTACACTTGCTGACTTCGCTTT TGCCAATG ATTTCATCACAATGGTCCATATCACAGAACATAGAGATGTTTGGTAGAGGAGGACCAGCT CCTGGTGT TGGGTTTGGCTGGGGGACATGTGGTGGAGGGTTTTGGTCTCTTAAATGCCTACTTGCACA ATTGGATT CACAATTGGTTGTAGAATTGATCAAATGTTTCTCTTCAGTTCAAGGAAGTCCTATCATCC TCGATGAA GGTGTGAAGTTAGATAATGTGACTAACACAGTTGTGACAGCTTCAAATTGGATCAGTTCT ACCCTAGG GTTGTCTCTGATTGCTGGACCTGGACAAATCTATATGTTGGAGAAGGTTTTCGATATGAT TTTTGAAC CTTCCATTCTGAAGTATCTCAAATCATCTATACATAAATTTACCTCTGACATGGAATTAC TGAAACCT TTTGAATGGGACTTAAATGAAGATGAATATATGCTCTTCAGCAGTGTTCTCAAATCACAT TTCAGATC CAGATGGTTAGCCATCAAGAAGAAGCATTCAGATAAATATGCAGGAGATAATAGCAGCAC CAAGATTT CAAAAACACCAGAGATATTGGAGACAATTCAAGAAGAAACAGAGTTGTCAGAAGCTGTAA ATCAACCT TGCAACACATTAATGGTAGAGTGGGCGCATCAGAGACTGCCTCTTCCTATCCACTGGATT CTAAGTGC AGTTTGCTGCATTGATGATCCAAAAGGCACACTCTCAACATCAGCCAACTATATTCTTGA TGTCTCAA GGGCTGGTCTTATCTTCCTTTTAGGTCTGGAGGCCATTTCAGCTACCCCGTGCCTTCATG CTCCTTTG ATCTGGAAAATTCATGCACTTTCGGTCTCTATCCGCTCTAGCATGCATTTGCTACAGGAA GACAGAAG TAGGGATATTTTCTGTGCTTTACAGGAACTGTATGGCCTGCATCTGAACAGGTTATACCA AAAATTCT GTAAACCAAACTCTATCGAGGAAGTTAAGGGCGTTGTAGTGGGCACTTCAGAGGAAGCGA TGGAGATC AGTAGCCTTGAAATTCTCAGGTTTCAGGAGAAAATTCATGGAAGCTATACTACTTTTGTT GAGAGCCT GGTTGATCAATTTGCAGCTGTCTCATATGGAGATTTTGTTTTTGGTCGGCAAGTGGCCAT TTATCTGC ATAGAAAGGCTGAGCCAGCAGTACGTCTTGCAGCATGGAATGCACTGTCTAGTGCGTATG TGCTTGAA CTGTTACCCCCGCTAGACAATTGCATTGGCAACGCCCCAGGATACTTGGAGCCTCTTGAG GTACATTT TCTTTAATTTATTTTGCATTTCTCTTCCAGAGAAACCTTTTCATGGAGTAACTATGTGAG TGATTTAT TTTGCAACTTGACCATGTACTCTTGTCTCTGTGTGTTGTAGAGCCTAGAATATGCAATAG GCACATCA TGATGCATTACTATTTTGCTGACATTTATTTTGGTTTCTTTATGTATGAAATCCATCCAC CATTTAGT ATGATGAACTTCTTTTGTTGGCTGCTTTTCCATGTTCAAAGGACAGTCTCACTTTGTCAA ATTTTTAC AATACTTCTGCAGGATGATGAAAAAATTTTGGAATCTTATGCTAAATCATGGACGTCTGG TGTCCTGG ACAAAGCTTTACAGCGTGATTCCATGGCCTTCACATTGGCAAAGCATCACCTTTCAGGCT TTGTCTTC CAGTCCAGCGATTCTGGCACAATGCTGCGAAAAAAACTGGTCAAATCGCTTATCCGGTGC TATGCACA

GAAGCGGCATCATGAGGTAGTTGGTCGCTCATGTTTCTTTGTTTGCTTGGTCCACGG CAATTCCTTCC ACGCCACTGTCTGAGTGTCTGTTGAATTCTGTACAACAGGTTATGCTTAAGTGCTTCGTT CAGCAAGG CATCGCACAGGATTCCAAGAGCAGTGAGCTTGACCGGAGATTTGAAATCTTGAAGGATGC TTGTGAGA TGAACTCCAACCTCGTAGGTGAAGTCCAGAGACTGAAGGCATGTCTTGGCCAATGAAGCC AGATATTT AAGTGTGTCATTAACTTGGCAGCGTTAGTTGTTGGGAAAGCTCGACAAAGTGGCCCAAAA TATGCAAC

TGAGGAAACTCACGGTCGGGGCTAGTGGTTACTTTTAATTTTGATGAAGGGAACGCC GAGCACGCAGC AACCCTGAGTCTAACCTGGCTATGGTTAGGCTGCTCTTAGCAGAGCATGCATATGGTCAT GTAAACAG TAGACCACACTGTCTATTGAGTGAAGTTTGAAATAGACTTTATATATAGCATTAGGCTTC CTTTGATT CC

SEQ ID No: 20 MINIYO Glycine max, >GM01G08040, Gene

ATTCCTGGACAAAGAGCCCTTGCATTGCATCTCCTTTCGTCTGTGCTTGATAAGGCA TTACACTATAT TTGCAAAGACAGAACAGGGTATATGACAAAAAATGAGAACAAAGTTGACAAATCAGTTGA CTGGGAAG CTGTTTGGGCTTTTGCACTGGGCCCAGAACCTGAGCTTGTGTTGTCACTTAGGTAAAGTT TGCTTTTT

GGTCCAAGCTGTTGGTATTATAAACTACCTGCTATAACTGAGTGAAGATGCATGGTT TTCTTTTTCCT CTTTTAAGAAAATGAATAATGTTGTTTATATTGCTGTTAATCATTAAGCATACAAGTTGA TTGGTTTG GATGTAAGTAAAATTCCAGCTAGGTTTTATGTGTGTAATTTTAATATCACTTCCATCTGG CGTGTGAC ATATATCTGGTTCCATTACTGAGTATTTACATGTCTTGCACCCTAGAAGCCAGCCTTATT TGTGGTAA AATGTTTTATAATATTATTATGCCTTAGAATACTTTAGAGTATCTTAGTTAATCTCGAGA GTGGTTTC CATATTTAATTATTTTTGATGATTTTTTAATTATTAGGAATTTAGGATTTGGAACCTTGT CTTAAGGA TGAGGGTTAGTGCTTTGTCTTTTGTAAAATATCATTACACACCAATGAAGATAAAATTCT CTCCTATT CTCTTTATTTATTTAAATCCCCATAATATGAACCTGGTTCCGAAGTGATCCCATCATCTG TGATTTGA CCCCATCACTTGCTGCCTTGTTCTCTAAACGGGTGCTCATCTTTGTTTCTGTGTTTTTTT TTTTCTTT TAATTTTTGGTCGCTGTGTCCTTAGTCCTTGAGGATTCTTATCCTCTTATATTTGTATCT TTCTCTTC

TATCTTAATATATTCTTTGCTTATATAAGCTTTGTTGATTATTATGCTTTGGGATGA GCTCTTGTGTA TACTGGCTTTTTCTAATCTGTGCCCTTTTTTTGTGGTCTTCATCCTAAAACTGTGATGAT CATCATAT GTTAAAATGGATGCTGGTTGGCCCTTGGACCCTTAGGGAATTTTACTTCCTGCATAACTG TTTCTAAA ATTCAATTGGAAGAGTGGGAATCTAGATTGCATACTTGACTCACACCTTCTGTCCTCTTG TATTTAAT AATATGGAGTGTTGGTGAGGCTATAAAGATTTTTTATTATGAATTATAAATTACTAAATG CAAATAAA TGTCATCCCAAATAGATGGCTATATATCTTGTCAATATGTTTGAATTTTGCCTATAGATG GTATTATT ATGTTGTAATCCATGTGGTATTTTGAGTTGCTTATGATAAATATACTGATGAATACTTTA ATTCTTTC AAATTGTATTAGAGTTTAATGCCCATGCATTGGTAGTGTAAAAAAGTTTGACACTGTCAT CCAATAAC AAATCAATGTTTGAATTACTTTAAAATAATTATTTTATAAGTCAAAAAACTTACCATTCA TTGTGGGT TGTGATTGGATAACTGTAAAACTTTTTACACTGTCAGTACATAATCCTTTTTCTCATTGT ATTATCAT AAATTTATTTTTTTCCTCATTATATGGGCATCTTTTGACGGCAGTTGTGCTCTAATTTTG TAGGATAT GTCTTGATGATAACCACAATTCTGTAGTTCTGGCCTGCACAAAAGTTGTTCAATCTGTAT TGAGTTAT GATGCAAATGAGAACTACTGTGATATGTCAGAGGTAACTGGATTTTTATTATCTTTTAAT TTGACAAT ATTATTATGTTTAAAATTAGATTCATCTGATTTTTTATTTTAATTCCAGAAGATAGCAAC TTGTGACA TGGATATTTGCACGGCTCCAGTTTTTAGGAGCAGACCAGATATTAATGATGGATTCCTTC AAGGGGGT TTCTGGAAGTACAGTGCCAAACCTTCTAATATTCTTCCTTTCAGCGATGATTCAATGGAT AATGAGAC TGAAGGAAAACATACTATTCAAGACGATATAGTGGTTGCTGCGCAAGATTTTACTGTAGG TCTAGTTC GCATGGGAATCCTTCCTAGGCTTCGTTATCTTTTGGAGGTAAAACATAATTAATCATTGA TCATGCTG AAACATTTGATGTCATGAGACTCTATCTACAAAGATTAAGGATATTTTTGTTTTATGATG TTTGAACT TCCTTGTCAAATTCATTATTCTCTAATGGTTGCAGAAAGATCCTACAACAGCTTTAGAAG AATGTATC ATTTCTATACTGATTGCTATAGCGAGGCATTCACCTACATGTGCTAATGCTGTACTGAAA TGTGAAAG ACTTGTTCAGACAATTGTGAATAGATTTACTGCTGACAATTTTGAACTTCGATCTTCTAT GACTAAAT CTGTAAAACTCTTGAAGGTGAGTGGTAATTTTCCATTTTATTTTATAGGAAGTGATTTCT ACATCAGC AGCCAGAGAATCATTCCTAATGTTTCATTTGATTTTGGAAAAGGTGTTTGCTCGGTTAGA CCAGAAAA CTTGTTTAGAGTTTATAAAGAAAGGGTATTTTCAGGCTATGACTTGGAATTTATATCAAA GTCCTTCC TCCGTTGACCACTGGCTAAGGCTAGGGAAGGAAAAATGTAAACTCACATCTGCTCTGATT GTTGAACA AATGCGTTTCTGGAGGGTCTGCATTCAATATGGATATTGTGTGTCTTACTTCTTGGAAAT GTTCCCTG CCTTGTGTTTTTGGTTGAATCCACCTTCATTTGAAAAACTTGTTGAAAACGATGTTTTGG ATGAATCT ACTTCCATCTCTAGGGAGGCATACCTTGTTCTGGAGTCTTTGGCTGGAAGGCTTCCTAAT CTATTTTC

AAAGCAGTGTCTAAACAACCAACTTCCAGAGTCTGCTGGTGACACCGAGGTATGGTC TTGGAATTATG TTGGTCCAATGGTTGACTTAGCCATAAAGTGGATAGCAAGCAGAAGTGATCCAGAAGTAT CCAAGTTC TTTGAGGGACAGAAAGAAGGAAGATGTGACTTTCCTTTCCGAGATCTTTCTGCAACTCCT TTGTTGTG GGTGTATGCTGCTGTGACTCGCATGCTTTTCAGAGTGCTTGAAAGAATGACATGGGGGGA TACTATCA GCTCTTTTGAAACTGAAGGGCATGTGCCATGGCTTCCAGAATTTGTACCTAAGATTGGAC TTGAGTTG

ATCAAATATTGGTTTTTGGGCTTTTCTGCATCCTTTGGGGCAAAATTTGGAAGAGAT TCTGAAGGTGA ATCTTTTATGAAGGAACTAGTTTATTTGAGGCAGAAGGATGATATTGAAATGTCTTTAGC TTCCACCT GTTGTCTAAATGGAATGGTCAAGATTATTACTACAATTGATAATCTGATACTGTCTGCCA AAGCTGGC ATCTGTAGTCTCCCACGCCAAGAACAAAGTCTCTCAAAAGAAGGAAAAGTGCTTGAGGAC GGCATTGT TAATGGGTGTTTGGTTGAGTTAAGGTATATGCTTGATGCTTTCATGTTTTCAGTTTCTTC AGGGTGGC

ACCACATACAGTCCATTGAGTCATTTGGCAGAGGAGGACCAGTTCCAGGGGCAGGAA TTGGATGGGGT GCCCCAAGTGGAGGATTTTGGTCAGCAACATTTTTATTGGCACAAATAGATGCAAAATTT CTCGTCTC TTTGCTGGAAATTTTTGAAAATGCGTCTAAAGGTGTTGTGACTGAAGAAACAACCTTCAT TATCCAAA GGGTGAATGCTGGCTTGGGATTGTGTTTAACTGCAGGACCTAGAGAAAAGGTTGTTGTAG AAAAGGCA TTGGATCTCTTGTTCCATGTCTCTGTTTTGAAGAACCTTGATCTCTGCATACATAATTTT CTCTTCAA

TAGAAGGGGTAGAACTTTTGGCTGGCAACATGAAGAAGAGGATTACATGCACTTAAG AAGAATGTTAT CATCTCATTTCAGGAGCAGATGGTTGTCTGTAAAGGTGAAGTCTAAATCTGTGGATGGCA GTAGTTCC TCTGGCATTAAGACCTCTCCAAAGGTTGGTGCTTGTTTGGAAACCATATATGAGGATTCA GACATGTC TTCCATGACAAGTCCGTGCTGTAATTCTTTAATGATAGAATGGGCTCACCAGAAACTACC ACTTCCAG TTCACTTTTACCTTAGTCCAATCTCAACAATTTTCCATAGCAAGCGGGCTGGTACTAAAA AAGTTGAT GATGTACTACATGATCCATCTTATCTGATTGAAGTTGCCAAATGTGGACTTTTCTTTGTT TTAGGTGT TGAAGCAATGTCCATTTTTCATGGCACTGACATTCCTTCTCCTGTTGAACAAGTATCATT GACATGGA AGTTACATTCCTTATCTGTCAATTTCCTTGTTGGAATGGAGATACTTGAACAAGATCGGA GCAGGGTT ACTTTTGAAGCTTTGCAGGATCTTTATGGTGAGCTTCTTGATAAGGCAAGGTTAAACCAA AGTAAAGA AGTTATTTCAAATGATAAAAAGCATCTTGAGTTTCTGAGGTTCCAAACTGAGATTCATGA AAGTTACT

CAACTTTTCTTGAAGAACTTGTGGAGCAGTTTTCTGCTGTTTCTTATGGTGATGTTA TTTTTGGCCGG CAAGTTTCACTTTATCTACACCGTTATGTTGAAACTTCCATTCGACTTGCTGCCTGGAAT ACACTGTC CAATGCTCGTGTTCTTGAGCTTTTGCCACCTTTAGAAAAATGCTTTTCTGGTGCTGAAGG ATACCTTG AACCTGCTGAGGTAAAAAAAATAATCATTAACTACCAGCTATTTTACTCTGGAGCATTAT TTGCAGAG GATATTGATTGAGTACTTGTTCTTTTGATACTTTTTTCCTTTCTATGTTGATGATATTGG GTTGAATA TATAAATGTCACTTATATTTTATATTTTATTATAATTTTGTAAATTTTCAAAAAGTGGTT GTTTAAAA TGCGCTTAAAAACAGAAAAGCGTATGCTACAAAGTACAGCTAATGTTGCAGAGTTTAACT GTGTTACA AAATTTACAATACCTTTGACATTTATTGGTTGTATTGTAGCATCTGTCATGAATTTTGAG GAAGCTTT TGAGAGCACAGGAAATACCAAAATAAGCCATACTGATACTGGGTCCTTTTATTTTTTATA TGATGCAT AATAAAGTGAAGTTCCTAATTGGAATTTTGGATATAGTGAAGGATCTTATACTTCCAGCA ATATAACA GATAGGGTCACTTAGCACCAAACATGCACATATTTTTTACAATGACATGTTTTTAAAGCT TGTCTTTA GTAGGGAAGAAATGTAAGGTTGTATCTTTGATACTTTGAAGTTAGAAACTATCACGATGG CTTTGTTG TGTAAGTTACCGTGAGGAATGAGGATTGTTGTTCATCAAGTTTCCTTATCTAAATTTTTT TATTTTCC ATTTTTTGTTAATATCTATAACTTCTGTGAATAGCAACAATTGGAAATGGGTAGGTGATA ATTGTTTA CTACTGTATTATCTGTGGAGGGGTGCACTTGCCACCTGTGTGGTTGCACCAGCAATGCAT ACTAGTCA TTGGCTCAGAATACACCATATATCTATCAACATTAATGGTGTACTGTATCTCTGCAGGAT AATGAAGC CATTTTGGAGGCTTATACGAAGTCGTGGGTTTCTGATGCCCTTGACAGGGCTGCAATTCG AGGATCAG TTGCATATACTCTTGTTGTCCATCATCTTTCCTCCTTTATATTTCATGCCTGTCCCATGG ATAAGTTA TTGCTGCGAAACAGACTTGCTAGGTCTCTGTTGCGAGATTATGCTGGGAAACAGCAACAC GAGGTAAC CAAAGTCTTAAAAGCTTTTATCCTGATGGACAAATGGTAGTTTAAGCAAATCACCATTCA GAGCTTGT GCTGCCATTCATTCTCCAATTAGTTTTATCCCATCTGATTATGGAAATCAAATGTTATAT GTGAATGT GTGCTGTGCACGTGTGTGCTTGTTCTGTCATCACGTTGTTTGGAATGTATCAGCTAGGAC TTTGGCCT ACCTAATAAAATTTTAAGAGTGTGCAGTGAGACATCACTGTTTAGGTAAATCCTAGTTGC AGTATTTT TATTACCAAGAATTTGAGGCCATGGAAGAAGTATAAGATTTTGTCCTATCTTTTTCATCC TAATTTAA TTTGCATTGTTGCGTCTGTATTTACGATTATATAGCCATAATGTTGGTGTAGCCAGACAT TACTAATG GAACCCTTGTTGCAGGGTATGTTACTGAACCTCATTCACCATAACAAGCCGCCACCATCT GTCATGGG AGAGGAGCTGAATGGTGGTGTACTTTCTGAAAGGAATTGGTTAGAGTCCAGATTAAAAGT ATTGGTTG AGGCTTGTGAGGGAAATTCCTCTCTTTTGATAGTAGTAGAGAAGTTAAAGGCTGCTGTAG AAAAGAGT TCATAGTGAGGTAACTAATATATCGAATGCTTGTAAATATATTCGAGATATACGATGAGT ACAACTAA GGTTTATATATAGATTTTTGCAATGGGGTCTCAAATGCATTAATTGGAGCATACATGGCC ACTGATAT

TGATATTTTTTGTTAGAATGGAGTCTGCTGATTTTTTAATCGAGTCCTAAGGCATGC AATGTACATAA TGAAGGAATACAAGTATTTTAGTCGGGTTATTATAAAATACACTGTTTCACTCC

SEQ ID No: 21 MINIYO Glycine max, >GM02G13360, Gene

GAGTTTGAAAAAGTTTCAGCCTTTGCCAAGCCGGTACAGAGGAGGAGGAAAAAGGGT TTGGATTTTAG AAAATGGAAAGAGATCACTCGGGATGATAGTTCTTCCTTCGGGAAGGAATCAGAGAAGGA TGTGTCAA GCTTTAGCCAAACTACTGGGAAAAAGAAGAATGAAAAGGGCAGTAAGAGCACATACAAGA AAACCTCA TCTTTGGATGATAATGTCATTTCTCCAATGAAAGTGGATACAAAACCACTGTTAGATAAC TCAGATGG TGGGTTTATCAATTCAACTACCACTATGGAAGTAGATACATTAAATAAGGTAGATCATGA GGAAAAAG

TTAAACACGCCAGAATTTATGATGACAAGGAGCAAAATGAATCTGTGCCTGGATTGG ACCAAATTTCT TCTGATTGGATGCCTGATTACAATTTTGGATCCCTGGATGTGCAAAGGCCAGGGCAAACT GACTTGAA TTCAAGCATGCTGTCTTGTTCTAGTTCCAATAGTATTAGAAGTGAACAAAAGTCCGTGTC TCTTGATA GTGAAATTGATGCTGAGAATCGAGCTCGGATTCAGCAAATGTCAGCTGAGGAGATTGCAG AAGCCCAG ACTGAGATAATGGAGAAGATGAGCCCTGCATTACTAAAATTACTGCAGAAGAGGGGGCAG AATAAATT

GAAGAAACTAAAATTAGAAGTGGATATTGGCTCAGAATCTGTGAATGGACATGCTCA GAGTCCTCAGG ATGCAAAACATCTACACACAGAGGATGGGATCGCTCAAACAGTGATTGTGCCACCATCCA AAGAAAAG CTAGATGATGAGAAAATTAGCACGAAGACTTCAACCACCGCTAGTAGTAGTGCATGGAAT GCTTGGAG CAATAGAGTTGAGGCTGTTAGGGAGCTACGATTTTCCTTGGTTGGGGATGTTGTTGATTC TGAACGTG TATCAGTTTATGGTATGCGTTTCTATTCTTCTTATGTTTCTTTACTATCTTCTGGTTCTA ATATCAAG ATGATGCTTTGTATGATCCTTGCATATGTATATATATTAGAGTATCTCCTTGTACCATTC TGGACTCT GTAGTTAACTAACAAGTGCCGGCTAAGAATTCTGTTATTAGTCAGTTGTAACTGACAGAT TAATTTCA GCTAGGCTATCTCTATATATCTCAGACATACCTCTTCTATTTGCGATCAATGAATAAACA TTTTATCA GTAATCACTCTGAATATCTCAGTGCTCTCTTTCTCTCTCTGCTCGATGAATCCTAACAAT ATATGGGT TCTTCTGTATTTAGTGTTTTGCATATGTAGGTGCTTGGTTAGTGATAGTAATAGTATTGT CTTCTTAA

TGTAGATATATGCTCTTCTGTAATTTTTTTTTCTTTATTGGGTATGTGGTAAAGCTA GTGATAGTTTG GGTTGCTAATGTTTGAATACTTTGCTTCATGAAACATCAACCATTGTTTATAGATTGTGA TTTGTATT CAATATTATACATTATACTACCTCCAGACTAAAATATAAGCAACAAAAAATCAATGTGTT TGGGTTAA AATATAAACAAATTTTAACTAACTCTCTCCTATTTAATGATAATATCTCCAAAATACCCT TCATTTAA TTAGAGTTTTATTTCCAATAAACTTCTCTTTTTTGTCCTATGCAATTAATGTAAATGGTA CTTTAGGA AATAAATTAACTTTTTTTATTGAGACTAACAAAATTAAATAATGCTAACTAATTTTATTG ATGAGTGT GAATTAGTTTTTTTTGCTTATATTTCAGTCCGGAGGGAGTAGTATTTTTTGTTCCCAGCA ATTGATGA TCTTTTTTTGGTTGACTACATTTCTAAATGCACATGAACCAAAAAAAACACTTACTGTTT GTTTAACT TATTTGGAGAAATAATCACATTTTTTCTGGTTTCTGAGAGAGATTTTGAAAAATTGGCGA TTATTAAT CCAAATTTAATCTTTATCAAACATTTTAGCATTTCCATGTGTCATGTAGGCAATATATTG CTGGTAAA TACAAATACAGGAAAGTTAAGATCAATGATGTTGCTATATCATGGCTTGTCTGATAGCAC TGAGTAGA TTATGCTCCCTGCCCCCCTGCATTTGCCACAAATTACAATAATGTTCTGGTTCATGCCTA GACTGAAA TTTCTGTATGGTTTCCTTTGCTTCCAAATGTTTCCAAGTTCATAGACTTGATTAGATGGC TTCTGTTG TATATTCAGCATATTAGATGTTAGCATTTGCATATAACAGAACGGAGGTGCAAATATTGA TTTAAATA ATGAATATTCATGGATATCCATTGATATCCTGATTATTCTGTTAGCACTGATATCCATCA AATCTTAG CATTTGTTGTATATTACTATATTCATTGATATCCTGTTTATTTTGGAAATAGGATGGAGG TTTAAATA TAAATTTTGAATTTTCTTTATGTGACAATTCTTTGTCATGATACAGACAATGCCAATGAA CGTGACTA TCTACGGACTGAGGGAGATCCTGGTGCTGCCGGTTATACAATTAAAGAAGCAGTGGCACT CACTAGAA GTGTGGTATGTTATTTGTTGTAACTGATGTATATTTCAGTTGGATGCCTGGACCTGGAAC AGTTTGGA TGGCTTTACAATTATGAATATAAAATATATAAATTTATAGCATTCCCCTTTAGTAACACA GCGTCTGC CAAATGTTTTGTTTTTTTAGATTCCTGGACAAAGGACCCTTGCATTGCATCTCCTTTCAT CTGTGCTT GATAAGGCATTACACTATATTTGCGAAGACAGAACAGGGCATATGACAAAAATTGAGAAC AAAGTTGA CAAATCAGTTGACTGGGAGGCTGTTTGGGCTTTTGCACTCGGCCCAGAACCTGAGCTTGT GTTGTCAC TTAGGTAAAGTTTACTTTTTGGTCCAAGCTGTTGGTATTATAAACTACCTGCTATGACTG AGTGAAGA TGCATGGGTTTCTTTTTCTTCTTTTAAGAAAACGAATATTGTTGTTTATATTGCTGTTAA TCATTAAT CATACAAGTTGATAGGTTTGGATGTAAGTAAAATTCCAGCTTGGTTATGTGTGTAATTTT AATATCAC TTTCATCTGGCATGTGAGATGGACTCAATGAAGCTTGAGATCACATATCTATCTGTTTAC ATTACTGA TTATTTACATGTCTTGCACTCTTGAAGCCAGCCTTTTTTGTGGTAAAATGTTTAATATTA TTATGCCT TAGAATACTTTAGAGTATCTTAGTTAATCTCTTGAGAGTGGTTTCCATATTTAATTATTT TTCATGAT

TTCTTAATTAATTAGGATTTGGAATCTTTTCTTAAGGATGAGGATTAGTGCTTTGTC TTTTGTCACAT ATCATTACACACCGATGAAGATAGCATTCTCTCCTATTCTCTTTATTTAATTAAATCCCT ATAATATT AACCTGGTTTCAAAGTGGTCCCATCCTCTGTGATTTGACCCCATCACCTGCTGCCTAGTT CTCTAAAC TGGTGCTCATCTTTGTTTCTGTGGTTTTTTTCTTCCTTCCAGTTAGCTGTCTTTCCTTCT GCCATTGT CTATCTTTTCTTCTTTGTATGTAAAGATTTTGATCTGTCAAATTTGATGCCTAATTGCCT TATCTCCT

AGTTACTGCATGATGTCCAGATTGAGCTATGGTTCTGGTTCTCATTTGTTCTTACAT TGCCCAGCAGT TTCCTTTCTCTGGAATAATTTGTTTAGTGTTTTCATAGAATATGGGGTTCGTCCCTAGAA TCTTCAGC ACTTCCTGTATGTTAATTTTGGAGGATTTGGTACTAGCTGAGAATCCAGAAAGTTTTGGT GTTCTTCT CTGTGTGAAGTTCTTTGGGTATATTCAGTTAGAAATCATCTTCTGTGGATGATAGTCTTC TAATGAGT TCATTCGGGTTCAGCTAGTTTTTCTAGCTTCTTTGTGGTGTTCTGCTTATGGTCTTTATA TATAAGAT

TTTATTTTTGTTTGATTGATTGTGTGTTTCTTAATCTTTGTTTTTTTCCTTTAATTT TTGGTTGTCGT GTCTTTAGTCCTTGAGGATTCTTATCCTCTTATATTTGTATCTTTCTCTTCTATCTTAAT AAATTCTT TGCTTATATAAGCTTTGTTGATTGTTATGTTTTGGGATGAGCTCTTATGTATACTGGCTT TTCCTAAT CTGTGCCCTTTTTTGTGGTTTCTTCCTAAAACTGTGATGAGCATCATATGTTAAAACAGA AGCTGGTT GGCCCTTGGACCCTTGGGTAATTTTACTACCTGCATAGCTGTTTCTAAAATTCAATTGGA AGAGTGGG

AATGTAGATTGCATACTTGATTGACTCATAATACCTTCTGTCCTCTTGTATTTAATA ACATGGAGTGT TGGTGAGGCTAGAAAGATATTTTATTTTGAATTATAAATTACTAAATGCAAATAAATGTC ATCCCAAA TAGATGGCTATATATCTTGTCAATATGTTTGAATTTTGCCAATAGATGGTATTATTATGT TGTGACTT GTGATCCTTGTGCTATTTTGACTAGCTTATGATAAATATACTGATGAATACTTTAATTCT TTCAAATT GTATTTTTATAATTTTTTTCCTCATTATATGGCCATCTTTTGACAGCAGTATTGTGCTCT GATTTTTT GTAGGATATGTCTTGATGATAACCACAATTCTGTAGTTCTGGCCTGTGCAAAAGTTGTTC AATGTGTA TTGAGTTATGATGCAAATGAGAACTATTGTAATATCTCAGAGGTAACTGGATTTTTATTA TCTTTTAA TTTGACAATATTGTTGCGTTTAAAATTAGATTCATCTGGTTTTTTATTTTAATTCCAGAA GATAGCAA CTTGTGACATGGATATTTGCACGGCTCCAGTTTTTAGGAGCAGACCTGATATTAATGATG GATTCCTT CAAGGGGGTTTCTGGAAGTACAGTGCCAAACCTTCTAATATTCTTCCTTTCAGTGATGAT TCAATGGA

TAATGAGACCGAAGGAAAACATACTATTCAAGACGATATAGTGGTTGCTGGGCAAGA TTTTACTGTAG GTCTAGTTCGCATGGGAATCCTTCCTAGGCTTCGTTATCTTTTGGAGGTAAAACATAATT AATCATTC ATCATGCTGAAACATTTGATGTCATGAGATTCTGTCTACAAAGATTAAGGATATTTTTGT TTTACAAG GTTTGAACTTTCATGTCAAATTCATTATTCTCTAATGGTTGCAGACAGATCCTACAACAG CTTTAGAA GAATGTATTATTTCCGTACTGATTGCTATAGCGAGGCATTCACCTACATGTGCTAATGCT GTACTGAA ATGTGAAAGACTTGTTCAGACAATTGCAAATAGATATACTGCTGAAAATTTTGAAATTCG ATCTTCTA TGATTAGATCTGTAAGACTCTTGAAGGTGAGTGGTAATTTTCCATTTTATTTTACAGGAA GTTATTTC TGCATCATCAGCTAGAGAATCATTCCTAATGTTTCATTTGATTTTGGAAAAGGTTTTAGC TCGGTCGG ACCGGAAATCTTGTTTAGAGTTTATAAAGAAAGGGTATTTTCAGGCTATGACTTGGAATT TATATCAA AGCCCTTCCTCCATTGACCACTGGCTAAGGTTAGGGAAGGAAAAATGTAAACTCACATCT GCTCTGAT TGTTGAACAAATGCGTTTCTGGAGGGTCTGCATTCAATATGGATATTGTGTGTCTTACTT CTCGGAAA TGTTCCCTGCCTTGTGTTTTTGGTTGAATCCGCCTTCATTTGAAAAACTTGTTGAAAACA ATGTTTTG GATGAATCTACTTCCATCTCTAGGGAGGCTTACCTTGTTCTGGAGTCTTTGGCTGGAAAA CTTCCAAA CCTATTTTCAAAGCAGTGCCTAAACAATCAACTTCCAGAGTCTGCTGGTGACACAGAGGT ATGGTCTT GGAATTATGTTGGTCCAATGGTTGACTTAGCCATAAAGTGGATAGCAAGCAGAAATGATC CAGAAGTA TCTAAGTTCTTTGAGGGACAGGAAGAAGGAAGATATGACTTTACTTTCCGAGATCTTTCT GCAACTCC TTTGTTGTGGGTGTATGCTGCTGTGACTCACATGCTTTTCAGAGTGCTTGAAAGGATGAC ATGGGGGG ATACTATTGAAACTGAAGGGCATGTGCCATGGCTTCCAGAATTTGTACCTAAGATTGGAC TTGAGGTA ATCAAATATTGGTTTTTGGGCTTTTCTGCATCTTTTGGGGCAAAATGTGGAAGAGATTCT AAAGGCGA ATCTTTTATGAAGGAACTAGTTTATTTGAGGCAGAAGGATGATATTGAAATGTCTTTAGC TTCCACCT GTTGTCTAAATGGAATGGTTAAGATTATTACTGCAATTGATAATCTGATACAGTCTGCCA AGGCTAGC ATCTGTAGTCTCCCATGCCAAGAACAAAGTCTCTCAAAAGAAGGAAAAGTGCTTGAGGAT GGCATCGT TAAAGGGTGTTGGGTTGAATTAAGGTATATGCTTGATGTTTTCATGTTTTCAGTTTCTTC AGGGTGGC ACCGCATACAGTCCATTGAGTCATTTGGCAGAGGAGGACTGGTTCCAGGGGCAGGAATTG GATGGGGT GCCTCAGGTGGAGGATTTTGGTCAGCAACAGTTTTATTGGCACAAGCAGATGCAAGATTT CTTGTCTA TTTGCTGGAAATTTTTGAAAATGCATCTAAAGGTGTCGTGACTGAAGAAACAACCTTCAC CATCCAAA GGGTTAATGCTGGCTTGGGATTGTGTTTAACTGCAGGACCTAGAGATAAGGTTGTTGTAG AAAAGACA TTGGATTTCTTGTTCCATGTCTCTGTTTTGAAGCACCTTGATCTCTGCATACAGAGTTTA CTCTTGAA TAGGAGGGGTAAAACCTTTGGCTGGCAACATGAAGAAGAGGATTACATGCACTTAAGCAG AATGTTAT CATCTCATTTCAGGAGCAGATGGTTGTCTGTAAAGGTGAAGTCTAAATCTGTGGATGGCA GTAGTTCC

TCTGGCATTAAGACCTCTCCAAAGGTTGGTGCTTGTTTGGAAACCATATATGAGGAT TCAGACACGTC TTCCGTGACAACTCCGTGCTGTAATTCTATAATGATAGAATGGGCTCACCAGAAACTACC ACTTCCAG TTCACTTTTACCTTAGTCCAATCTCAACAATTTTCCATAGCAAGCGGGCTGGTACTAAAA TTGTTGAT GATGTACTACATGATCCCTCTAATCTGCTTGAAGTCGCCAAATGTGGACTTTTCTTTGTT TTAGGTGT TGAAGCAATGTCCATTTTTCATGGCACTGACATTCCTTCTCCTGTTCAACAAGTATCATT GACATGGA

AGTTACATTCCTTATCTGTCAATTTCCTTGTTGGAATGGAAATACTTGAACAAGATT GGAGCAGGGAT ATTTTTGAAGCTTTGCAGGATCTTTATGGTGAGCTTCTTGATAATGCAAGGTTAAACCAA AGTAAAGA AGTTATTTCAGATGATAAAAAGCATCTTGAGTTTCTGAGGTTCCAAACTGAGATTCATGA AAGTTACT CAACTTTTCTTGAAGAACTTGTGGAGCAGTTTTCTGCTGTTTCTTATGGTGATGTTATTT TTGGCCGG CAAGTTTCACTTTATCTACACCGTTGTGTTGAAACTTCCATTCGACTTGCTGCCTGGAAT ACACTGTC

CAATTCTCGTGTTCTTGAGCTTTTGCCACCTTTAGAAAAATGCTTCTCTGGTGCTGA AGGATACCTTG AACCCGCTGAGGTAAAAAAACATATTCATTCACTACCAGCTATTTTACTATGGAACATTA TCCGCAGA GGATATTGTTTGAGTACTTGTTCTTTGATACATTTTTTCTTTCTATGTTGATGATATTGG GTTGAATT ATAAATGTCACCTATATTTTATATTTTATAATTTTGTAAATTTTCAAAAAGTGGTTGTTT AAAATGTG CTTAAAAGCATAAAAGCATATGCTACAAAGTACAGCTAATGTTGCAGAATTTTTAATTGT GTTACAAA

TTTACAATACCTTTGACATTTATTGGTTGTATTGTAGCATCTTTCATGAATTTTGAG GAAGCTTTTGA GAGCACAGGAAATACCAAACTAAGCCATACTGACACTGGGTCCTTTTATTTTTTATATGA TACATAAC AAAAGTGAAGTTCCTAATTGGAATTTTGGATATAGTCAAGAATCTTATACTTCCAACAAT ATAACAGA TAGTCACTTTGGCACAAACATGCACATATTTTTTACAATGGCTTGCTTTAAAGCTTGTCT TTAGTAGG GAAGAAATGTAAGGTTGTATCTTTGATTCTTTGAAGTTAGAAACTATCACGATGGTTTTG TCATGTAA GTTACCTCGGAGGAATGAGGATTGTTTTCATCAAGTTTCCTTATCTAAAATTTTTATTTT CCATTTTT TTGCTAATATCTATAACTTATGTGAATAGAAACAATTGGAGCTCAATGGGTAGGTGGGAT AATTGTTT ACTACTGTATTATCTGTGGAGGGGTGCACTTGCCACCTGTGTGGTTGCACCAGCAATGCA TACTAGTC TTTGGCTCAGAATACACCATATATCTATCAACATTAATTGGTGTACTGTATCTCTGCAGG ATAATGAA GCAATTTTGGAGGCTTATACGAATTTGTGGGTTTCTGATGCCCTTGACAGGGCTGCAATT CGAGGATC

AGTTGCATATACTCTTGTTGTCCATCATCTTTCCTCCTTTATATTTCATGCCTGTCC CACGGATAAGT TATTGCTGCGAAACAGACTTGCTAGGTCTCTGTTGCGAGATTATGCTGGGAAACAGCAAC ATGAGGTA ACCAAAGTCTTGAAAGCTTTATCCTGATGGACAAATGGTAGTTTAAGCAAATCTCCATTC AGAATTTG TGCTGCCATTCATTCTCCAATTAGTTTTAGCCCATCTGATTAAGGAAATCAAATGTTATA TGTGAATG TGTGCTTGTTCTGTCATCAAGTTGTTTGGAATGTATATCAGCTAGGACTTTGGCCTACCA AATAAAAT TTTAAGAGGGTAGAGTGAGACATCACTGTTTAGGTAAAATCCTTTTTATGACCAAGAGTT TGAGGCCA TGGAAAAAGTATTATCTTTTACCTCCTAATTTAATTTGCATTGTTGCATCTGTATTTTCA ATTATACA TCCATAATGTTGGTGTGGCCAGGCATTACTATTTACTAATGGAACTCTTGTTGCAGGGTA TGTTACTG AACCTCATTCACCATAACAAGCCACCACCATCTGTCATGGGAGAGGAGCTGAATGGTATA CTTTCTGA AAAGAGTTGGTTAGAGTCCAGATTAAAAGTATTGGTTGAGGCTTGTGAGGGAAATTCCTC TATTTTGA CAGTAGTAGATAAGTTAAAGGCTGTTGTAAAAAACAGTTCATAGTGAGGTAACTAATATT GAATGCGT GTAAATATATTCGAGATATACAATGAGCTATACATAAAGTACAACAGAGGCTTATATATA GATTTTTT CAATGATGTCTCAAATGTATTAATTGGAGCATGCATGGCCACTGATATTGGTATATTTTG TTAGAATG GAGTCTGCTGGTTTTTTTATCAAGATTCTGGGAACCAAGTCCTAAGGCATGCAATGTACA TAATGAAA GGATACAGGTATTTTAGTTAGGTTATTATAAAATATACTCTTTCATC

SEQ ID No: 22 RTR1 Oryza sativa ssp. Japonica Os05g04370.1

MGPTTATDTGARMKPTTVASAVHRVQMALYDGAAASREPLLRAAASLLSGPDYADVV TERS IADACGY PACPNPLPSEDARGKAAPRFRISLREHRVYDLEEARKFCSERCLVASAAFGASLPPDRPF GVSPDRLD ALVALFEGGGGGGDDGGLALGFGASGDGKEVEEGRKVEIMEKEAAGTGEVTLQEWIGPSD AIEGYVPR RDRVVGGPKKEAKQNDACSAEQSSNINVDSRNASSGESGMVLTENTKAKKKEATKTPLKM FKQDEDND MLSSCISDS IVKQLEDVVLEEKKDKKKNKAAKGTSRVGKSKPAKRPVGRDGHEVDFTSTI IMGDRGSE MMDHGALGQYNFSSS ILANEQPSSSQYAAIDSVQAYTEELDELFSNAVNIAKDETSDDSGRCTLRSSL KAVGSKNAGHSVKWADENGSVLETSRAFVSHSSKSQESMDSSVRRESAEACAAALIEAAE AISSGTSE

VEDAVSKAGI I ILPDMVNQQQYNNDYDNDKDAGENEIFEIDRGVVKWPKKTVLLDTDMFDVDDSWHDT PPEGFSLTLSSFATMWAALFGWVSRSSLAYVYGLDESSMEDLLIAGGRECPQKRVLNDGH SSEIRRAL DTCVCNALPVLVSNLRMQIPVSKLEITLGYLLDTMSFVDALPSLRSRQWQLMVLVLLDAL SLHRLPAL APIMSDSKLLQKLLNSAQVSREEYDSMIDLLLPFGRSTQSQASLPS

SEQ ID No: 23 RTR1 Zea mays, GRMZM2G065622_T01

MSPPAPAAAAAAAPRTVASAVLRVQMALLDGAAVSSEALIHAAASALLSRADYDDVV TERTISDVCGN PACPNPLSSSSAAATGPRFHIALSEHRVYDLEEARKFCSERCLVASKALAASLPHDRPYG VPLDRLAA VVALVEGAAAGDGSGLGFQGLDGNGKVEDGGRKVEIKEKQVAGAGEVLLQDWVGPSDAIE GYVPRHDR

SAHGQKPQVQQNEGAGPELSRTENVDYGAAAPGEDGMTSSPSLVKTHVSSEVIVERM GSLVLGENTRT PRKKKTKTPSKMLEQEEDNSMLSSCISDS IAKQLEDVVLEERKGSQKNKMSKASSRAQKGKSTKRPAS TNMEENAMNQYNYLSSSVLVDNHPSSSQSSEKDSTQAYSEQLCEEFSEAVNIGNDETSDE KMRPAWKS SLKVAGSKSSRQSVTWADENGSVLETSKAYESPSSSIKRPEEGIDNSLRRASAEACAAAL VEAAEAIS SGTAEAEDAVSNAGI I ILPDMLNQQEHDNGKNSGGDDDPEIDRDVIKWPKKPVLLDTDLFEVDDSWHD MPPEGFSLTLSAFGTMWAALFGWISSSSLAYVYGLERGSVEELLIANGRECPEKTVLKDG LSLEIRRA LDSCVCNAVPVLI SNLRLQIPVSKLEITLGYLIDTMSFVDALPSLRSRQWQAVVLVMLDALSVHQLPA LAPVFSNSKLVQKMLNAAQVSREEYDSMVDLFLPFGRSVQAITPM SEQ ID No: 24 RTR1 Glycine max, Glyma02g34860.1

MAKDKPVSVKDAVFKLQMSLLEGIQNEDQLFAAGSLMSRSDYEDIVTERSITNMCGYPLC SNALPSDR PRKGRYRISLKEHKVYDLQETYMFCSSNCLVSSKTFAGSLQAERCSGLDLEKLNNVLSLF ENLNLEPV ETLQKNGDLGLSDLKIQEKTERSSGEVSLEQWAGPSNAIEGYVPKPRNRDSKGLRKNVKK ECPFI IMF NVRPMDVYGMTVNEMGFVSTI IMQDEYSVSKVPPGQMDATANHQIKPTATVKQPEKVDAEVVRKDDDS IQDLSSSFKSSLILSTSEKEEEVTKSCEAVLKFSPGCAIQKKDVHSI SI SERQCDVEQNDSARKSVQV KGKTSRVIANDDASTSNLDPANVEEKFQVEKAGGSLKTKPRSSLKSAGEKKFSRTVTWAD EKINSTGS KDLCEFKEFGDIKKESDSVGNNIDVANDEDILRRASAEACAIALSSASEAVASGDSDVSD AVSEAGIT ILPPPHDAAEEGTVEDADILQNDSVTLKWPRKTGI SEADFFESDDSWFDAPPEGFSLTLSPFATMWNT LFSWTTSSSLAYIYGRDESFHEEYLSVNGREYPCKVVLADGRSSEIKQTLASCLARALPA LVAVLRLP IPVSIMEQGMACLLETMSFVDALPAFRTKQWQVVALLFIDALSVCRLPALI SYMTDRRASFHRVLSGS QIRMEEYEVLKDLVVPLGRAPHI SSQSGA

SEQ ID No: 25 RTR1 Glycine max, Glymal0gl0540.1

MEKDKPVSVKDAVFKLQMSLLEGIQNEDQLFAAGSLMSRSDYEDIVTERSITNVCGYPLC SNALPSDR PRKGRYRISLKEHKVYDLHETYMFCCSNCVVSSKAFAGSLQAERCSGLDLEKLNNILSLF ENLNLEPA ENLQKNEDFGLSDLKIQEKTETSSGEVSLEQWAGPSNAIEGYVPKPRDHDSKGLRKNVKK AEMGFVST I IMQDGYSVSKVLPAIVKQLGKVDAKVVRKDDGSIQDLSSSFKSSLILGTSEKEEELAQSC EAALKSS PDCAIKKKDVYSVSI SERQCDVEQNDSAKKSVQKFQVEKAGEKKLSRTVTWADKKINSTGSKDLCGFK NFGDIRNESDSAGNS IDVANDEDTLRRASAEACVIALSSASEAVASGDSDVSDAVSEAGI I ILPPPHD AGEEGTLEDVDILQNDSVTVKWPRKPGISEADFFESDDSWFDAAPEGFSLTLSPFATMWN TLFSWITS SSLAYIYGRDESFQEEYLSVNGREYPCKVVLADGRSSEIKQTLASCLARALPTLVAVLRL PIPVSTME QGMACLLETMSFVDALPAFRTKQWQVVALLFIDALSVCRLPALISYMTDRRASFHRVLSG SQIGMEEY EVLKDLAVPLGRAPHISAQSGA

SEQ ID No: 26 RTR1 Sorghum bicolor Sb09g002730

MSSPAAAAAAEAPRTVASAVLRIQMALLDGAAASNEALLHAAASALLSRADYDDVVTERT IADACGNP ACPNPLPSSSSAAAATGPRFHIALSEHRVYDLEEARKFCSDRCLVASKALAASLPHDRPY GVPLDRLA AVVALVEGAAAAGDGSGLGFQGVDGNVKMKDEGRKVEIKEKEVAGAGEVSLQDWIGPSDA IEGYVPRR DRSAHGQKPQAEQNKVAGSDLSRTKNVDDRTAAPSEDGMTSPLSLVETHMSAEVMAERMG DLVLGENT KTLSRKKKTKTPSKMMEQEEDDSMLSSCI SDSIAKQLEDVVLEERKGSKKNKVSKASSRTHKSKSRKR PAGSDGHEVDFTSTI I IGDASTNREESAMNQYNYLSSSVLVDNHPSSSQSSAKDSTQAYAEQLCEEFS EAVNIGNDETTDEKMRPALKPSLKVTGSKSGRQSVTWADENGSVLETSKAYESPSSS IKQPNEGIDSS

LRRASAEACAAALIEAAEAISSGTAETEDAVSKAGI I ILPDMLNQKEYGDAKNNGGDDDPEIDRDVIK WPKKPVLLDTDMFEVDDSWHDTPPEGFSLTLSAFGTIWAALFGWI SRSSLAYVYGLERGSVEELLIAN GREYPEKIVLKDGLSSEIRRALDSCVCNAVPVLISNLRLQIPVSKLEITLGYLIDTMSFV EALPSLRS RQWQAVVLVMLDALSVHQLPALAPVFSNSKLVQKMLNAAQVSREEYDSMVDLFLPFGRSV QATTPM

SEQ ID No: 27 RTR1 Brachypodium distachyon Bradi2g38650

MAPHAAAAAAGTTRTTMNVATAVYRVQLALLDGAAASNEPLLHAAAAVLSRADYDDVVTE RSIADACG HPPCASPLPAAAAAAAAPPRFHI SLREHRVYDLEEARKFCSERCLVASAAFAASLPHDRPFGVPPDRL DALVALFEGGGDRPGLGFREVSSGKDKDEGRKLEIREKEAPGLGEVTLQEWIGPSDAIEG YVPRHHPI

PEGPMPEAKQRKTSRADQSRNKNLDSATSSSVEAPVSSEVIAKKLNDMVLGDNTKTK KKQVCETPSKM FRPDEHGDMLLSCVTDS IAKQLEDVVLEEKNDMKKERPTRASSRSRKSKPAKKPAGSDGHEVGFTSTI IMGDHVLAKMDQGPVGQYNFATS IADNQPSSSSSLSSSPTQYTARDLTGAYTEQLNKEFSKAVNLGKD EASDEKVRIVPKSSLKAGGSKNKSQSVTWADENGSLLEI SKEYVIHSDDKKHYKEDIDGSLRRESAEA CAAALIEAAGAISLGTSEVEDAVSKAGI I ILPDMLHQNQFKSDNGKNTVEKEI SETDNGVVKWPNKPV

FLDTDMFEVDDSWHDTPPEGFNLTLSAFATMWATLFGWI SRSSLAYVYMLDGSSVEELLISSGREYPQ KTVSKDSQSSEIKRTLATCIGNALPVLTSNLRMQIPVSKLETTLGYLIDTMSFVEALPPL RSRQWQLM VLVLLDALSVCRLPGLAPVMSDSKLLQKVLNSSQVSREEYDSMVDLFLPFGRSVQTPPPS QPVQVP SEQ ID No: 28 RTR1 Oryza sativa ssp. japonica , >OS05G04370. Gene

CTCTTCGTCTCGACTCTGAACTAAAAACTCAACTCCTCCCAAAATCCCTCGCCGCCGCCG CCGCCGCC GCCGACGACGACGACATGGGCCCCACCACGGCCACCGACACCGGCGCGAGGATGAAGCCC ACGACCGT CGCGTCGGCGGTGCACCGCGTCCAGATGGCGCTCTACGACGGCGCCGCGGCGTCGAGGGA GCCGCTGC

TCCGCGCGGCGGCCTCGCTGCTCTCGGGGCCGGACTACGCCGACGTCGTCACGGAGC GCTCCATCGCC GACGCCTGCGGGTACCCGGCGTGCCCCAACCCGCTCCCCTCGGAGGACGCCCGCGGCAAG GCGGCGCC GCGGTTCCGCATCTCGCTCCGGGAGCACCGCGTGTACGACCTCGAGGAGGCCCGCAAGTT CTGCTCCG AGCGCTGCCTCGTCGCCTCCGCCGCCTTCGGGGCGTCGCTCCCGCCCGACCGCCCCTTCG GCGTCTCG CCCGACCGGCTCGACGCCCTCGTCGCGCTCTTCGAGGGCGGTGGTGGTGGTGGTGATGAC GGTGGGTT GGCGCTAGGGTTTGGGGCGAGCGGCGATGGGAAGGAGGTGGAAGAGGGGAGGAAGGTGGA GATCATGG AGAAGGAGGCGGCTGGGACGGGGGAGGTGACGCTGCAGGAGTGGATTGGGCCGTCGGACG CCATCGAG GGCTATGTGCCTCGCCGTGATCGCGTCGTTGGAGGTGAATCGCCTTTTGCTGACCTCTTC TATTTCTA TTTGCATTGAGCATTGATTGGTTTTTCTGTTCAAATTATTTACTCGTTTGGTTTGATTGT GCTGCCAT AGGTTAGTAGTACGATGAGTGAGGTTTATGGCGGTGGCATTCTCTGTTATCCTTTGTGCT CAAATTAG GTAGAGAAAAAACTTTGGAAGATAGAAAATGGAGGAATTTGTAGTGTTCGTAGTAAATTA CTTTGAGT ATCAACAATTGTTGTTGCTAGTAGCAGTTAGGAAAATTCTCTGTAACATGTACAACTACA ACATTTTG GTGAACTAGTTATAAACTCCTTGTGTAAAATCTCCCTACCTGATTAGCAAATTAGTAGCA TTTGTGTA TGACTAGAAACAATCAACTAGGTAATAATTGAGAGCTATCAAATATGGTAAGGGACAGCT GAAGAATA GACATAACCGTGGTGCCATATTTTTTGGTTGCAGTCATTCAAATTACAAGAGGACAACTA GGCAATTC ACTCATTTTGTTTAGACCTACATATTGTTGTTGATAAGGGACGCTAGAACGAAGATAGGA GATTGAGA GAGTAATTAATTTTTGGAAGTACGTTACAGATTTTAATGGGAGGTAGTGACTTCTTTTTT GAGAGATT AGAGGGGTGAGAGATGAGCTGCTTACTTTGTCAATGAAAAGCGCTCAGGTTTTGTTCAAT ATTTCCCC GAAGAAATACAAAAATCATGTCTTTGTAAGCATCATGTGTTGTTCCTCTTTTCTCACTGC TCACGGAG GTGCCTAAACTGCCTAACAAGGTGGCAAACTGGTCCCTAGTGCCTAAACACCAAGCCACC AAGGCAGT GGTGGTTTGGTGGGAGTGTGGTGGTACTTAGCTCCTACCTCCTAGGCACTGTTTGTTTTT CTTATATT CAAATAATGTTCTAGAACTAGATGTGACAATGTTACAAGAGTAACAATAGTTTTACTTGC AGGCACAT TTATATATATGAAAAGGATATGCTCATTCTTGCTCTTTGTTCGACCTGTCTTAGTTTCGA ACAATTGA AGAAACAATGAGCTTGTGTTCTGTATTTCAGGGCCAAAAAAAGAGGCTAAACAGAACGAT GCTTGTAG TGCTGAGCAGTCCAGTAATATTAATGTGGATTCTAGGAATGCTTCTTCTGGTGAATCCGG CATGGTTC TTACTGAGAATACAAAAGCAAAGAAAAAGGAAGCAACCAAAACCCCATTGAAGATGTTCA AGCAGGAT GAAGATAATGATATGTTGTCGTCTTGCATATCGGATTCCATTGTGAAGCAGCTGGAGGAT GTAGTTCT

CGAAGAGAAAAAGGATAAGAAGAAAAATAAAGCAGCTAAAGGAACATCGAGGGTAGG TAAGAGTAAGC CTGCAAAAAGACCAGTTGGGCGTGATGGACATGAAGTGGACTTTACAAGTACAATTATTA TGGGTGAT CGTGGTTCAGAAATGATGGATCATGGTGCTCTGGGTCAATATAATTTCTCAAGTTCTATA TTAGCAAA TGAGCAGCCTTCATCATCTCAATATGCAGCGATAGATTCAGTGCAAGCTTACACTGAAGA ACTAGATG AATTATTTAGTAATGCAGTTAACATTGCAAAAGACGAGACAAGTGATGATAGTGGTAGAT GTACACTA

AGATCTTCATTGAAGGCTGTTGGATCCAAGAATGCAGGGCATTCTGTGAAATGGGCA GACGAGAATGG AAGTGTGTTAGAGACAAGCAGAGCATTTGTAAGTCACTCCAGTAAATCTCAAGAAAGCAT GGACAGTT CAGTAAGGCGTGAATCTGCAGAAGCTTGTGCAGCTGCGCTTATTGAAGCAGCAGAAGCTA TTTCATCT GGCACATCGGAAGTAGAAGATGCAGGTGAACACTTATTCCTTAACCCTGTGGTGCTTTGA CATGCAGC TTTTGTTTTTGATATGTATTAACCTGTGCCTTTTGGTAACAGTTTCAAAGGCAGGAATCA TCATACTG

CCGGACATGGTTAACCAGCAACAGTACAATAATGATTATGACAATGACAAAGATGCA GGGGAAAATGA AATATTTGAAATTGATAGGGGTGTTGTGAAGTGGCCGAAGAAGACTGTGCTTCTAGACAC AGATATGT TTGATGTCGATGATTCTTGGCATGATACACCACCAGAAGGCTTTAGTCTAACTGTAAGAA TTCTTGAG AAAAAATAAAGTAGCACTTCTTCTTTTTTTTCCTTCTGGTTGAATTTGGCATGTCATGCC TTTTTTCC TTTTCAGCTGTCCTCCTTCGCAACGATGTGGGCTGCATTATTTGGATGGGTATCCCGGTC CTCATTGG

CCTATGTGTATGGGCTTGATGAAAGTTCTATGGAAGATTTGTTGATTGCAGGTGGAA GAGAATGTCCT CAGAAGAGAGTTTTAAATGATGGCCACTCATCTGAAATTAGAAGAGCTTTGGATACTTGT GTGTGTAA TGCCCTGCCAGTTCTTGTATCAAACTTGAGGATGCAAATTCCAGTCTCAAAGTTGGAGAT TACTCTGG TATGGATAAAGCTAGTTGAACAAACTAATTAAAAAGTTAAAACATTTTTTAAAAGAAAAG AATAAGGA CTCCGCAATTGGTTAGTGACCTAGTTGAACCTGGATATGTATTTACTGGCTAGTACATAT AGTTTTTC AGCAGCGGCTGTGAAGAGGCTTTTCGTTGCATTTTGTTCTGGTATCTAGACACCTTTGAC TGAGATCA ATCAAGCTACTAATATCTTGGTCAGTTTAACAATAATTTCTTAGTCATTTGGGGTTCTCT CTCATTCA TAAGTGTGGGTGATGAGCTGCGCATATCTGGAAATAGATAAGACGAAGTGGAGGCTGTAC GTTACAGT TATTCTGAATTAGGGCCAGTCTCTTTTTTGTTGATTCTATTGAAGACAGCTTAACTGCTA GATGTTGC CACCAAGAATTTTATTTGTTAGTTTGATTACAGTTTCAGTAATTAACATTTAGAGCTATA ATTAGTGT

GCATCTAATGTGTTTTTCCCCTCCCCACTAGGGATACTTGTTGGACACGATGTCATT TGTTGATGCAC TGCCTTCTCTGAGATCAAGGCAGTGGCAATTGATGGTTCTCGTGCTGCTTGATGCGCTCT CACTCCAT CGGCTTCCTGCTCTTGCTCCAATAATGTCAGATTCGAAGCTTTTGCAGAAGGTGATGATG CCTTTCCC TGCCTTTCTGCTATGCAAGTAGACGGATGCACATATTCTTTTTAAGAAATCTGATCTTTC TTCCCTTT TGTGTGCTGCAGCTTTTGAACTCGGCTCAGGTTAGCCGAGAGGAGTATGACTCCATGATT GATCTCCT CCTCCCTTTTGGAAGATCCACGCAGAGCCAGGCATCCCTGCCAAGTTAAACCTCAAGCAA CACAAGTA TCTAAATACATGTTTACACAGCGGAGTAAATAGAGAGAGGTTCTACATATCAGCGTCAGC TTGGCAGT CTATTCGGATATACTATCATAATGGTGCCTCTTGCGTCTGGTTGTTTAGGTTTCGGAACA CGTCTTGC AAAATATCGGTTGCTCCCAGTTGCTTCAACTATCCCCTTTGCATTGGCGTCAGACGTACA AGCGGAGC GGGCACTGATTCCTGTCATTCTCAGGAATTGTTAGCTTTAGTGAGGAGAGCAAAAGATAA CTGCCTCC AGAACAATTTGGTCCACTATGGACTTTTATCTCTCATTGCTAGCGCAGTTCAGAATTGTA GTGCATCT TTGGGTTTTTTTTTTACCTCTTTTACCGGTGTGCAGTTTGTCAGGTTAGTACAGCCGAAT TTGACCAG CTAACAACCCACTCGTGAGTCCTAATAGGTGAGTGCTAGATATCAAGTGGTATAGTAAAC CCAGTGTT AGCATCTATAAAATTCTGAATTTTATGCCTGTCAATCTCGC

SEQ ID No: 29 RTR1 Zea mays , >ZM08G20550, Gene

GCTTGAACTCATTTGCAATTGCGAACGCTTCTTCTCCCAGTCCCAGCACGCCCAACCCCG TCGCCGCC TTCTCGAACCTTCCGAAGATGAGCCCCCCGGCCCCGGCCGCCGCGGCGGCGGCGGCGCCG CGAACGGT CGCCTCGGCGGTGCTCCGCGTCCAGATGGCGCTCCTCGACGGCGCCGCGGTGTCCAGCGA GGCCCTCA TCCACGCGGCCGCCTCCGCGCTCCTCTCCCGCGCCGACTACGACGACGTCGTCACCGAGC GCACCATC TCGGACGTCTGCGGCAACCCCGCGTGCCCCAACCCTCTCTCCTCCTCCTCCGCCGCCGCC ACGGGGCC CCGCTTCCACATCGCCCTCAGCGAGCACCGCGTCTACGACCTCGAGGAGGCGCGCAAGTT CTGCTCCG AGCGCTGCCTCGTCGCCTCCAAGGCCTTGGCCGCCTCGCTCCCGCACGACCGGCCCTACG GGGTCCCG CTCGACCGCCTCGCCGCGGTCGTCGCGCTCGTTGAGGGCGCCGCCGCAGGGGACGGGAGC GGGTTAGG GTTCCAGGGACTGGATGGGAATGGGAAGGTGGAGGACGGGGGAAGGAAGGTGGAGATCAA GGAGAAGC AGGTCGCCGGGGCTGGCGAGGTCTTGCTGCAGGACTGGGTTGGGCCCTCCGATGCCATTG AGGGTTAT GTGCCGCGCCATGACCGCAGTGCTCATGGTGAGTATCCCATACTTTGTTTGCCCATGATT GCATTTTA TTATTTTGTAAATATCAATTGATTGAATGACGGAAAGGCGAGAACAGAGCCCAATGGTGG TGTTAGTG TCTTGTCGTAATGCTGAAATATTGCATGGAGATATGTTGCTTTAGACTTCAGTGTTGCAG TTTATGTA

TTTGGTCTTATATATTTCCATAGGTGTTTGCTCATGAATAACTTGGGTAGGTTGAAT TGGTTTCCGGA ATAAGATATGATTCTATGTTGATATTGTTACTTTTAAGTTTTTAACATGTAAATATAAGT AATCTTTA CCTGTGGTTGTGTCGCAATTAGTAGTTTATTTGCATCCTGCTAGTGCATCTAGTTAGCAA CCTTTTTG TATACATGAAGACTATTTGGGTGAAAGGAGCCAAACTTGACACCTACTTGCATATTTTCC ATGTGATG ATCGTGTCTATGGCGGTTGACGTGTGCAGCCTGCAGATGTTTGTGTTATTGTTTAAGTGT GTATGCTA

GTAGAAATTAAAGAAAAATAGAACAATAGAGGTTGTTGCTCAATGGTTTTCTGACTA TTACTCCTTTG CACCATGATGTGTTGAGGTCATTCACCCTTGGAGTTTTAGTCAGTACCCTTGATTTAGGG TCTGTTTG GTTGGGCTGTGGCTGTGGAAAAAGTTGCTGTGGGCTGTGAGCTGTGGAAAAAGCTGCTAT AGGCTGTG TGCTGTTAAAAAGCTAAAAATCGTTTGGTGGAAACCACTAAAAGTCGTTAAAAGTTCTTT GATATATG TTTTCACAGTTCCATCCAAAAGCCACTAAAAGCAGGTCCAGGGGTGCTTTCAGTTTTGCA CTACGAGA

AAGTCGGCTTTTAGAAAAAGCTGCTTCGTGGATCCAGCCCTTTGGTTGGCTTTTGGC TTTTAGGGGGC AAAAGCCAAAGCCAAAAGCCAAACCAAACACACCCTTAGTATCTCTACTGCTGCATTTTG CACATCAT AACTTTGCTACTGATGCAGTTCAGCCTGCACTTTGCAGCACACTGACAATTTATAGGGTC CTGCCTGC AAGCATCTTGGGGTTGATATTGATTTAACACACCAATTTTTTAGTCACTGGTGTAAGTAA GAATGTTT ACCAGAGTAACGGTAGTTTTTCTTGCATGCACATTTCTGTACATGAAAGGATCCTTATCT CCATTCTT

GCCCTTTGTTCGACTTGTCTTAAATTTTGAACAATTGAAGATACAGTGAGCTTATGT TCTGTTGTCAG GACAAAAGCCACAGGTTCAGCAGAACGAAGGTGCTGGACCTGAACTGTCCAGAACTGAGA ATGTGGAT TATGGTGCTGCTGCTCCTGGTGAAGATGGCATGACAAGTTCACCTTCATTGGTTAAAACA CACGTGAG CTCCGAAGTAATAGTTGAGAGAATGGGCAGCCTGGTTCTTGGTGAGAATACAAGGACGCC TAGAAAGA AGAAAACTAAAACTCCATCAAAGATGTTAGAGCAAGAGGAAGATAACAGTATGCTGTCAT CTTGCATA TCTGATTCCATTGCCAAGCAGCTTGAGGATGTAGTTTTGGAAGAGAGAAAAGGCAGTCAG AAAAATAA AATGAGTAAAGCATCATCAAGAGCACAGAAGGGTAAGTCTACAAAAAGGCCTGCTTCGAC AAACATGG AGGAAAATGCTATGAATCAGTATAACTACTTGTCAAGTTCTGTATTGGTAGACAATCACC CCTCATCA TCTCAATCTTCAGAAAAAGATTCAACACAGGCTTACTCTGAACAACTGTGTGAAGAATTC AGTGAAGC AGTGAACATTGGAAATGATGAGACAAGTGATGAAAAGATGAGACCTGCATGGAAGTCTTC GTTGAAAG

TTGCCGGGTCTAAGAGCAGTAGGCAGTCTGTTACATGGGCAGATGAGAATGGAAGTG TCCTAGAAACA AGCAAAGCATATGAAAGCCCTTCAAGTAGTATAAAACGACCTGAGGAAGGCATAGACAAT TCACTAAG GCGTGCATCTGCTGAAGCGTGTGCTGCAGCACTTGTTGAGGCAGCAGAAGCTATTTCTTC AGGCACAG CAGAAGCAGAAGATGCAGGTGAGCATGTATTCATTATGTTCCCACGGCTGCTATTCTTTG AGGCTAAC AACTTTTGTTATTAAATGATACTGACGTAAGCCTCTCTAACGTCAGTTTCAAATGCTGGA ATCATCAT TCTGCCTGACATGCTTAACCAGCAAGAACATGACAATGGCAAAAACAGTGGCGGAGATGA TGACCCTG AGATAGATAGGGATGTTATCAAGTGGCCTAAGAAACCTGTACTTCTGGATACAGACTTGT TTGAAGTT GATGATTCTTGGCATGACATGCCTCCAGAAGGTTTTAGTCTAACTGTAAGTATTATTAAG AAGGGAAA AAAGAGAGGAGAAATTCCAGTTTTGCTTTTAATTCGGTCTCAGCACGATGTACATTTCTT TTCAGCTG TCTGCTTTCGGGACGATGTGGGCCGCGCTATTCGGATGGATATCCAGTTCGTCTTTGGCC TATGTGTA TGGGCTTGAAAGGGGTTCAGTGGAGGAGTTGTTGATTGCCAATGGGAGGGAATGTCCTGA GAAGACAG TTCTGAAGGATGGGCTCTCATTGGAGATTAGAAGAGCTCTAGATTCTTGCGTTTGTAACG CCGTGCCA GTACTCATATCAAACTTGAGGTTGCAGATACCGGTTTCAAAACTGGAGATTACTCTGGTA CGTGTCAA CTTTACCAAGCAGATAATAATATCGTACCTTTTTTAAAATAAGGCTGCTATAGGTTTAGC TTGATGCT GGTGGCTGACAGTTATATCGGCGGTAACACATGATGAAACTACACCGTGTCTGTACCAGG GCTACTTG ATTGACACAATGTCGTTTGTTGACGCCCTGCCTTCTCTGCGATCGAGGCAGTGGCAGGCT GTGGTTCT GGTAATGCTTGACGCGCTCTCTGTGCACCAGCTTCCCGCCCTTGCTCCAGTCTTTTCGAA TTCGAAGC TTGTGCAAAAGGCGAGTGACCAGTTTTTTTGTGGTTAGTTGAATAATATATGTATATCTT ATTTTGCT TTGGTGACATCTGAATTTGTTTCCCCATCAATGTGCGATGCAGATGTTGAACGCTGCTCA GGTTAGCA GAGAGGAGTATGACTCCATGGTGGACCTGTTTCTACCGTTTGGAAGATCCGTCCAGGCGA TCACGCCC ATGTAAACGAGAAGCCGTGTGAATCTGCATTCCGGAAGCTGCGTGAATCGTAGGGTCTGA TCTGATAT TTAGTTTTACACAAGTCGCTGTCTAGAACGAGCCATGTATGTATGATTGATTGGTTATCT ATTGAGCA AGATGCGCTCTGGCAATTTGTGGAAGCTGAAATACTTGCGACCATGACGCCTGCCTGTCA GTTTGCGA TATTCTTTCAGGTTGTGAGAAATTGATTTGCTGTCGTTCTCAGCTATTGTTAGCTTTATG CCCTCTTT GAACTCCTAGAGCTAATAGTTAGCCAGCTAAACAGCCGAGCTAGCTAATAAACTAACTAA GCTAACTA ATAAACTAATTATTAGTTGTGAGTTAGCTAACAATTAACTGGACTATTAGCCTTGGATCT GAACTTTT CCCCCTCTGCTCCTGTTTATCCCTGCGTTTTTACTTATATACAACGGGCAGTTTCACGTA ATTACATG GGCAGTTTCACGTAATTACATGACATTTTTGGCATTGTGTAGAACTCATAAAGCTAACGC TAATAGAG TGTGTTTGGTTTGGTTTGGTTTTAGCTTTTGACAATTAAAATTCAAAAGCTAAACCAGAG GGTTCGAT

CCAGTAAACATTTTTTTTCTCTAAAAATCGACTTTCTCATAGCACAAGACAGACTGA AAGCATCTCTT CACCTATTTTTAACGGCTTTTGGATGAAACTGTGAAAATATATATGGAAGAAATTTTAGC ATCTTTTA TTGGCTTCCACCAAACCGATTTTTTTGTTGCTTTTTTTACATTTCATAGCCCACATTAGT TTTTTATA GCTCACAGCACACAACAACTTTTTTCATAGCCACAACCCAAACTAAACACACCATAGTTA GCTAGCTA ATAATTTGTTAGCTTGAATAACCTAATTAACTGTTAGCTAGGATCTACTAATTTTTTATA GTACCTTG

CTAAAAGTAAATGGATTTCACACTCCAAACATAACACAAACAACACCAGTCTATTAA AAAACATATAA AA

SEQ ID No: 30 RTR1 Glycine max, >GM02G34860, Gene

TTCAAGCTATTTGGTTCTGAAGCTTTTGTTCAATGGCAAAGGACAAGCCTGTTTCTGTCA AAGATGCC GTCTTCAAATTGCAAATGTCACTCCTTGAAGGCATTCAAAATGAAGACCAGCTGTTTGCT GCCGGGTC TTTGATGTCAAGGAGTGACTACGAAGACATTGTAACCGAACGATCCATCACAAACATGTG TGGTTATC CACTCTGCAGCAATGCTTTGCCATCCGATCGCCCGCGGAAGGGTAGATATAGGATTTCAC TGAAGGAG CACAAGGTCTATGACCTACAAGAGACTTACATGTTTTGTTCTTCAAATTGTCTTGTTAGC AGCAAAAC

TTTTGCTGGGAGCTTGCAAGCTGAGAGATGCTCTGGTTTAGACCTGGAGAAACTAAA CAATGTTCTTA GCTTGTTTGAGAATTTGAATCTGGAACCGGTGGAGACTTTGCAAAAGAATGGAGATTTAG GTTTGTCT GATTTGAAAATCCAGGAGAAAACAGAAAGAAGCAGTGGGGAGGTGTCTTTGGAGCAGTGG GCTGGACC TTCAAATGCAATTGAGGGATATGTACCAAAACCAAGAAACCGTGATTCTAAGGGTTTGCG GAAAAATG TTAAAAAAGGTGAGGATTTTTTTGGGTTTTCTAGACAATTGTGAGAAACTAATCAGTTAG CCATATGC GATTTCTTGCTTAAGAGTGTCCTTTTATTATCATGTTTAATGTTAGGCCTATGGATGTTT ATGGCATG ACTGTGAAGTCTGAGGCTGAGGCTTAATTTATGTGAAATGGAATACTATAATTACTATTT CTTATCCT TTTTTCTCTATCCAATCAAGTGAGCTTTGATTCTGCATTGCAGGGTCCAAAACTGGTCAT GGCAAGTC AATTAGTGACATAAATTTAATTAACAGTGAGATGGGCTTTGTGAGTACTATAATTATGCA AGATGAGT ATAGTGTTTCAAAAGTACCGCCAGGTCAAATGGATGCAACTGCTAATCATCAAATTAAAC CAACAGCT

ACAGTCAAGCAGCCAGAAAAGGTTGATGCTGAAGTGGTCAGGAAAGATGATGATAGC ATTCAAGATTT GTCTTCATCTTTTAAGAGCAGTTTAATTTTAAGCACCTCAGAAAAAGAGGAGGAAGTAAC TAAATCAT GTGAAGCTGTGCTCAAATTCTCCCCCGGTTGTGCTATTCAAAAGAAAGATGTTCATTCAA TCTCCATA TCAGAAAGACAATGTGATGTGGAACAGAATGATTCTGCTAGGAAATCTGTACAAGTCAAA GGGAAAAC GAGTAGAGTTATTGCTAATGATGATGCTTCCACTTCCAATTTAGATCCTGCCAATGTTGA AGAGAAAT TCCAAGTGGAAAAAGCAGGTGGATCATTAAAGACTAAACCCAGATCTTCCCTTAAATCTG CTGGTGAA AAGAAATTTAGTCGCACTGTTACTTGGGCGGATGAGAAAATCAACAGCACTGGGAGTAAA GATCTTTG TGAGTTTAAAGAATTTGGAGATATTAAAAAAGAATCTGACTCAGTAGGAAATAATATAGA TGTTGCCA ATGATGAAGATATATTACGTCGTGCGTCAGCAGAAGCTTGTGCTATTGCATTGAGCTCAG CATCAGAA GCAGTTGCCTCTGGAGACTCGGATGTCAGTGATGCTGGTAATTACTGTTTCTTTTACGAG TTTTCTAT TTAAATTAATTGGTCTGTAAAAGTTTTCTCGCCTATGAATGAAACTTGTGCAGTTTCTGA AGCTGGAA TCACTATATTGCCACCTCCACATGATGCTGCTGAGGAAGGTACTGTGGAGGATGCTGATA TACTACAA AATGATTCAGTTACTCTGAAATGGCCAAGAAAGACTGGAATTTCTGAAGCTGATTTCTTT GAATCTGA TGACTCATGGTTTGATGCTCCACCAGAGGGTTTCAGTTTGACTGTAAGTTTAGTGAAAAT TTTAGAAA CATTCAAAGCTGTATTAATTTCCACAGTATATTCTATGGCATAACTTGTGCTTTCTTTCT TTCCTTTC TTTTTTTTTATAATTTTTTGTTTGTTTGTGTGTGTAACTTTATTTCAGTTGTCACCTTTT GCAACTAT GTGGAATACCCTCTTTTCATGGACAACATCATCTTCTTTGGCATATATATATGGGAGGGA TGAAAGTT TTCATGAAGAATATCTATCAGTTAATGGCAGAGAATATCCTTGCAAAGTTGTCTTGGCAG ATGGTCGC TCATCTGAAATAAAACAAACTTTAGCCAGTTGTCTTGCTCGAGCTTTACCTGCGCTTGTT GCTGTGCT CCGGCTGCCAATACCAGTATCTATCATGGAGCAAGGGATGGTAGGATCTTGGAGTTATCT ATTTTTGT AGTTTATTTTGTAGTATAGTTGTCCCAAACTAAGAGTCATTACAGATTTATTATACTTCA GCAGGCAT GGTCTGGTTTGTTTTACACCATTCATTGGGACTTAAAGGAAAATCATTTAATATAAGCAT ATGCATGT TAATTTTTGTGAGAAATAGATATGGATCCATTGCTTGAAATAAGAGACACGTGGAAATTA AAATATTT GAGCCTGTAGGATAAATACTTCATGCTATTGAAAAGAAAAGAAATAGAATTTGGGGAGAG GGGGTGGG GTGCTGCTGAGCCCCTTGTATCCGTCCCTGCCTGCATAGTCCTTGCTATTTAAATTCCTT AATCATTA TGTGGTTCGATTCAGGGAAAATCTGCAATAATTGCAAGATACCTAGTTGCATTGGTCTAA GCACTTAA ACAAACTAATAGTGACTTCTTTTTGCTGGAAGCAAATACTAAAATGATTTCTCCATGTTA CATTGATT TAGCATCTGCAACACATTAACTGCTTTTGGTTGACAATTAGGAGGATTCTTGGGTTTTAA AATTATGC CTTATTGTCTGAGAAGACAATATAATTTTTGAGAATCAGTTTAGAAATCAGTGAAAGTAG GGGAGTCT

TGGCACAGGGGTTTCAAGCAATGGCATCAGCTTCTTGCAGAGACAATGCTGGTTACT ACTTCCTACAC ATATTGGGTCCTACCCTTCCCTGACCCAACACATAGCTTTATAGCACAAGGTTCCCTATT TTTAAAGT TTAGAAATTTCTAAATTCATGAGTTTTAGGCTATAAGTTGCAGATGGATTTAATCTTCAT ATCTGTAT TGAAAAATTCTTTAATATATCCATTTACTTGGTGCATGGATGGGTTATATGTTAATTCTC GTGACTTT CTATTAGGCATGCTTGCTGGAGACAATGTCATTTGTGGACGCACTTCCAGCTTTCAGAAC AAAACAAT

GGCAAGTGGTTGCTCTTTTGTTCATTGATGCATTGTCCGTATGTAGATTACCTGCTC TTATCTCATAC ATGACGGATAGGAGGGCTTCATTTCATAGGGTGAGAACCTTTTGTTTATATCATACTAAT TTATTATT TTATATACATGATGGATAGGAGGAATCTGTTTGCGGTGCATGAAGCATTATATAATGATG TTGGGTTG TATATATATTCAGGCAAAAAAAGCATAATCCCATATTATGGCTCTGATCTTTTGGTTAGG GTAGTTCA GTTAACATCTGATATCTCCATTATTTCAATTGCTAAAATTTTGGTTACTTTTCATCTGCA TTTCCTTT

ATAAATGTTTTGTTGCCCAATTCTTGATCAAATGGGAGCTTAACAACATAAATCCCA CACAACTTAGC TACAATGTGCTTAATGTTGTTCCCCTTCTATAGCTTTAGACTCGATGGCCTTATTTTATG ATTCTATA GTTTAGTTCATCTAGTGTGGTTCTCCACTTCTCCTACCATGGCTGTGGACTTTAAATTCT TGTTTGGT TTTCCATCATGTATTTTCATGCTAATTTTGTTTGAAGTCAGCTAAACCACAAGTCGTGCA CATAGATT GCCATAGGCACAAATTTATGGCACGTGGACATGGAACCCAACTTGGAAATTTTTTTCTTC TAATTTGA

TTCCCTACATATGTGTGTTGGGGTTGCAACAATTTTGATATGACAGCTGGAATATGG AGGTTAATGAT ATATCTTATTGTTTTGTTGTTTTATCTCCTGTTATGTCAGATTTTGATGTTATAATTTTC ACTCTTCT TTTGAACCTGTTAACCATTGTTCTGGTATTGATTTGGCGAAACAGGTTTTGAGTGGTTCT CAAATACG TATGGAAGAGTATGAGGTTTTGAAGGATCTTGTAGTACCACTGGGCCGAGCACCTCATAT CTCTTCCC AAAGTGGGGCATGACAACAAATAAATGTTGGACTTCACCAACGATGAGCGCAATATTATA TGCTCTAA TGCTAGCTAGCGAGTGATAAATGCAAATTGATATTCAAAATAGACATTGTTCTAAAATAT TGTCTTCC TGTTAAATGGCAGTTTGTATGTTTTTATTTTATTTTATGCCAAGCAGTCTGTAGAAGGTT CTGAAGAT GTCTATTGGATTACTAATCTTAGAGGTGCATGTCAGGATGGTTAATACAGAACAAATATC TTCCCGAT TATAAGATTGATTTTACAGATTTAATTT

SEQ ID No: 31 RTR1 Glycine max, >GM10G10540, Gene

GCTGAAAGGAAAATAGAGGTTTCTCTTTCAAGTTTCACCTCCTCACCACCGCCAAGCTTC GTCTCCGA GAATGTCACCATCGCACACTTTTTTGTTTCCAAGCACAGCACCGATGATATTAGCAACCA AACCCTAA TCGTGTCCACGCTTTCTTTCTTCTTTCCTGGCACACTTTCTCCCTCTCCACTTTCAGCAC ACACTTTT TCGTTTTCTGGTAAGTCCTAATTTAGAGAACTGTGTGATGGATTTGAAATTAGGGTTAAT GAAAGTGC ATTTCTTCTGTCCAAATTAGGGTTATCATGGAACCTAATTTTACGGTCTAAATGCGTTAA CGTTCAAG GACGACTACGAATGTGATTATTGTAATATATAATCATCAATGCAATTACTTTTATCTTTC ATGTGCTT TAATAATAGAATTATGATTGTGTCTTGTGACTCTGAAATTTTGTTGGGTTGAACTGTTGA AGCTATTC TTATTGTGGTGTACTTTGTGCATGATGCAGTTCTAGTTATTTGGTTCTGAAGCTTTTGTT TCAATGGA AAAGGACAAGCCTGTTTCTGTCAAAGATGCTGTTTTCAAATTGCAAATGTCGCTCCTTGA AGGCATTC AAAATGAAGACCAGCTGTTTGCTGCTGGGTCTCTGATGTCAAGGAGTGACTACGAAGACA TTGTAACC GAACGATCCATTACAAACGTGTGTGGTTATCCGCTCTGCAGCAATGCTTTGCCATCCGAT CGCCCACG GAAGGGTAGATACCGGATTTCACTGAAGGAGCACAAGGTCTATGACTTACACGAGACTTA CATGTTTT GTTGTTCAAATTGTGTTGTTAGCAGCAAAGCTTTTGCTGGGAGCTTGCAAGCAGAGAGAT GCTCAGGT TTAGACCTGGAAAAACTAAACAATATTCTTAGCTTGTTTGAGAATTTGAATCTGGAACCA GCGGAGAA TTTGCAAAAGAATGAAGATTTCGGTTTGTCTGATTTGAAAATCCAGGAGAAGACAGAAAC AAGCAGTG GGGAGGTGTCTTTAGAGCAGTGGGCTGGACCTTCAAATGCAATTGAGGGTTATGTACCAA AACCAAGA GACCATGATTCTAAGGGTTTGCGGAAAAATGTTAAAAAAGGTGAGGATTTTTTTTTTGGG TGTTCTAG AGTCTAGACAATTGTGAGAAACTATAGATAAATAGATAGCCTTATGCAATTTCTTGCTTA AGAGTGTC CTGTTTATTATCATGTTTAATGTTAAGCCTATGGATGATTGTGGCGTGACTGTGAAGTCT GAAGCTGA GGCTTAATTTATGTGAAATGGCATACTATAATTACTGTTTCTTATCCTTTTCCACTATCC AACCAAGT GAGCTTTGATTCTGCATTGCAGGGTCCAAAGCTGGTCATGGCAAGCCAATTAGTGACATA AATTTAAT TAGCAGTGAGATGGGCTTTGTGAGTACTATAATTATGCAAGATGGGTATAGTGTTTCAAA AGTACTGC CAGGTCAAAGAGACGCAACCGCTCATCATCAAATTAAACCAACAGCTATAGTCAAGCAGT TAGGAAAG GTTGATGCTAAAGTGGTCAGGAAAGATGATGGTAGCATTCAAGATTTGTCTTCATCTTTT AAGAGCAG TTTAATTTTAGGTACCTCAGAAAAAGAGGAGGAATTAGCCCAATCATGTGAAGCTGCGCT CAAATCCT CTCCCGATTGTGCTATTAAAAAGAAAGATGTTTATTCCGTCTCCATATCAGAAAGACAAT GTGATGTG GAACAGAATGATTCTGCTAAGAAATCTGTACAAGTCAAAGGGAAAATGAGTAGAGTTACT GCTAATGA

TGATGCTTCCACTTCCAATTTAGATCCTGCCAATGTTGAAGAGAAATTCCAAGTGGA AAAAGCAGGTG GATCATTAAACACTAAACCCAAATCTTCCCTTAAATCTGCAGGTGAAAAGAAACTTAGTC GCACTGTT ACTTGGGCAGATAAGAAAATCAACAGCACTGGGAGTAAAGATCTTTGTGGGTTTAAAAAT TTTGGAGA TATTAGAAATGAATCTGACTCAGCAGGAAATAGTATAGATGTTGCCAATGATGAAGATAC ATTACGTC GCGCGTCAGCAGAAGCTTGTGTTATTGCATTGAGCTCAGCATCAGAAGCAGTTGCTTCTG GAGACTCG

GATGTCAGTGATGCTGGTATAATTACTGTTTCTCTTACAAGTTTTCTATTTAAATTG ATTGGTTTGTA AAAGGTTTTTTCGCCTATGAATGAAACTTGTGCAGTTTCTGAAGCTGGAATCATTATATT GCCACCAC CACATGATGCTGGTGAGGAAGGTACTCTGGAGGATGTTGATATACTACAAAATGATTCAG TTACTGTG AAATGGCCTAGAAAGCCTGGAATTTCTGAAGCTGATTTCTTTGAATCTGATGACTCATGG TTTGATGC TGCACCAGAGGGTTTCAGTTTAACTGTAAGTTTAGTGAAAATTTTAGAAACATTCAAACC TGTATTAT

TTTTCAGTATATTCTATGGCATAACTTTAAACTTGTGCTTTTTCTTTTCTTTCTTTT TTTAATTTTTT TGTTTGTTTGTTTGTTTGTGTGTGTGTAACTTTCTTTCAGTTGTCACCTTTTGCAACTAT GTGGAATA CCCTCTTTTCTTGGATAACATCATCTTCTTTGGCATATATATATGGGAGGGATGAAAGTT TTCAAGAA GAATATCTATCAGTTAATGGCAGAGAATATCCCTGCAAAGTTGTCTTGGCAGATGGTCGC TCATCTGA AATAAAACAAACTTTAGCCAGTTGTCTTGCTCGAGCTTTACCTACACTTGTTGCTGTGCT CCGGCTGC

CAATACCAGTATCTACCATGGAGCAAGGGATGGTAGGATCTTGGAGTTATCAGTTTT GTAGTTTATGT TGTAGTATAGTTGTCCCAAATTAAGTCATCAGAGATTTATTATACTTCACCAGGCATGGT GGGACTTC TCTCATATGTTCATAAGCTCCCCTTCCCACAAAACATGCACATAGTCACACATATTCACA AAATATGA GATTGATAAATTTGATGTTAAAAATGAACTTTCAAACAGTGGTAAAGGAAAATCAGTTAA TATAAGCA TATGAATGCTACTTTTTGTGAGAATAGAGATGGATCCATTGCTTGAAATAAGAGACACAT GGAAATTA AAATATTAAGCCTGTAGGATAAATACTTTTTATTGATTGAAAATAAAAGAAATCGAATGG GAATTCCC CCCCCCCCCCCCCAGAGTAGATCCTGCCTGCATAATCCTTATTATTTCAATTCCTTGATT GTCATGTG GTTCAATTCAGGGAAAATCTGCAAGAATTGCAAGATCTAGTTGCAAAATTATGCCTTATT GTCCGAGA AGACAAAATATGTTTTCTGAGAATCAGTTTAGAAATTTGTGAAAGTAGGGGAGTCTTGGC ACAGGGGT TTCAAGCAATGGCATCAGCCCCTTGCAAAGACAATACTGGCTACTATACTTCCCACACAT ATTGGGTC

CTATGCTTCCCTGACCCAGCACATAGCTTTATAGCACAAGGTTCCCTATTTTTAGAA GTTCAGAAATT TGTAAATTCATGAGTTTTTAGGCTATAAGTTGCAGATAGATTTAATCTTCATATCTTTAT TGAAAATT CTTTAATATATCCAATTACTTGGTCTGTGGATGGGTTATATGTTAATTCTCGTGACTTTC TATTAGGC ATGCTTGCTGGAGACAATGTCATTTGTGGACGCACTTCCAGCTTTCAGAACAAAACAATG GCAAGTGG TTGCTCTTTTGTTTATTGATGCATTGTCCGTATGTAGATTACCTGCTCTTATCTCATACA TGACGGAT AGGAGGGCTTCATTTCACAGGGTGAGAACCTTTGTTTATATCATACTGATTTATTATTTT ATTTACAT GATGGATAGAAGGAAACTGTTTGCTGTGCATGAAGCATTATATAATGATGTTGGGTTGTA TATAGATC GATGCATTCCCTTATTACGGCACATGATCTTTTGGTTGGGGTAGTTCAGTTAACATCTGA TATCTCCG TTATTTCAATTGCTAAAATTTTGGTTACTTTTCATCTGCATTTCCTTTATAAATGTTGTC GCCTGATT CTTGGTCCAAATGGGAGCTTAACAACATAAATCCCACACAACTTAGCTACCATGTGCTTA ATGTTGTT CTCCTTCTATAGCTTTAGACTCGATGGCCTCATCTTATAGTTTAGTTCATCTAGTGTGGT TCTGCACT TCTACCATGGCTGTGGACTTGAAATTCTTGTTTGGTTTTCCATCTTGTATTTTCATGCTA AATTTATT TGAATGCAGCTAGACCACAAGTCGTGCACATAGATTGCCATGGCACAAATTTATGGCACG CGGACACT GAACCCAACTTGGAAATTTTTTCCTTCTAATTTGATTCCCTACATATATGTGTGTGTTGG GGTTGCAA AAATTCCGATGACAGCTGGAATATGGAAGTTCATGATATATCTTATTGTTTTGTTGTTTT ATCTCCTA TGTCATGTCAGATTTTGATGTTCACTCTACTTTTAAATTTGTTAACCATTGTTCTGTTAT TGATTTGG TGAAACAGGTTTTGAGTGGTTCTCAAATAGGTATGGAAGAATATGAGGTTTTGAAGGATC TTGCAGTG CCACTGGGCCGAGCACCTCACATCTCTGCCCAAAGTGGGGCATGACAACAAATAGTGCAT TTTTTTTT TATTTGGGGAAAATTTACCTGTCAAGCATTGGAGTGCTTGTTTATAAACATAAAAAATAT GCAATGAC AATTATGCTAGGCCTCTAGCAACACGGGAACCAGATTTCTATATTCTCTAATGCTAGCTA GAGAGTGA TGAATGCAAAATTGATATTCAAAATAGACATAGTTCTAAAATATTGTCTTCCAGTTAAAT AGCAGTTT GTATTTTTTTTAAAA

SEq ID No. 48 MINIYO promoter

TCATTTACCAAGTTTACAAAGATTATGGTCCAAGTCCTAAAACTGAATGAACATCACATA CCCGTCTC TTGAGTGATTTAATCATGTTCTTCATTGCACTAAAGCGACAACTTTTGGTTCAAATATAG ACTATGAC TATATGGTTTGTTTTGCACAGGATTAAAGTTGATGTTCCAATTTTATAATTAAAAAGTCA GAAAGGGG TTTTCTTGTTATTTTTTACTTGTTCTTATAAGCTATCGGGACGACACGGAGTTTTAAAGA GTTTTCCG TTTTGCTGAGCGGAGGCGAGAGAGGGTTTAGAGTGATGGAGCAAAGTAGCGGGAGAGTCA ATCCGGAA

CAGCCGAACAACGTCTTGGCGAGCCTTGTCGGGAGCATCGTGGAGAAAGGAATATCG GAGAATAAGCC TCCAAGCAAGCCGCTTCCCCCAAGGCCCTCCCTTCTTTCCTTCCCCGTCGCTCGTCATCG TTCTCACG GACCCGTAAGCCAATCCAATCCTCTAGTGCGTGCTTTTTAGGTTTCCATCTTCCTTTTGT TGCCTTCT TCTAGATTTTAAGCACCTTCTACTGTTGTTTAGTACTTGGGACTCCACAATTTTTCACCG TGCCTGAC CTTGTAATTCAGCTTTCTGAGACATCTAATTTTTGTTTCTCATGTTTGATTTTGTAGCAT TTGGCTC

SEQ ID No. 49 AtRTRl promoter

TGAATCATTTCTCAAAAAGAAAATGGGAAAAATGTCATTCAAATAATCAGTTTACCATTT TCGTTGGT TTTAAACATAAATTTTGGACCTGGTGATTTAAATCCTCAATATTATGTTGACTTTCAGTT TAAACACA

AATTTTCATTGATTAAGAGACATCGTTAGAAATTCCCTAGATCACATACCCTTTATC CCAAAACCGAA AACCGATTTTTGGATTCCCTCTTCTTCTTCGAATTCGAAGTAATCTCTTGTCTGGAGGTT GACTGATG GCGTAAAAAAAGAAGAATTTGTATCTCAATTAGTTTAGTTTACAAGAACTCGTGATTAAA TTGAAAGT CAAAATAAAAATGAGAATTTAAATTACCAAATCAAGAGTTTTCATATTTTAAATGGTAAA CTGATGAC ATTTTCCCTGTTGAACAATATTGGCCCATAATGTAACCCAATTACTCGGCCCAATTACGT GAACCGCC

TTTCACCTGGCTTAAGGAATAAGTAAGGACCATTCATGATCTCATCACTTTTAGCTT TCTGGCTTCTC TGCTTAAGCTCTCTCGAGTCTGCCTCAAGTGTTTTTGGGGGAAATTGATTTCGTTGAGAA AAACCCTA AATTCCGAACTTGAAGCAATTTTTCAATTTCGTTTGCAGAAAAATGGCAAAGGATAATGA AGCAATCG CCATTAACGATGCGGTTCACAAGCTTCAGCTCTATATGCTCGAAAATACCACTGATCAGA ACCAGCTC TTCGCGGCGAGGAAGTTAATGTCTCGATCAGATTACGAAGATGTCGTCACTGAACGAGCA ATCGCTAA GCTCTGTGGTTATACTCTTTGCCAGAGATTTCTCCCTTCCGATGTTCTAGAAGAGGGAAG TATCGGAT TTCGTTGAAGGACCATAAGGTTTACGATTTACAGGAGACGAGCAAGTTTTGCTCCGCTGG TTGTTTAA TTGATAGCAAAACGTTTTCGGGGAGTTTGCAAGAGGCTCGTACATTGGAGTTTGATTCGG TGAAGTTG AATGAGATTTTGGATTTGTTTGGTGATTCTTTGGAAGTGAAAGGTTCTTTGGATGTGAAT AAGGATTT GGATTTGTCTAAGCTTATGATTAAGGAGAATTTTGGAGTTAGAGGTGAAGAATTGTCTTT AGAGAAGT

GGATGGGTCCTTCTAATGCTGTTGAAGGTTATGTTCCTTTTGATCGAAGCAAATCAA GTAATGGTAAG TTCGATGATGAACTATGGTGTGAGCAAAAAATTTCAGTTAACAAATGTTTTATCGATGTG TAATAATT AAGTTTGGTTTTGGCAGATTCCAAGGCTACTACTCAAAGTAATCAAGAGAAGCATGAGAT GGATTTCA CTAGCACAGTAATTATGCCTGATGTTAATAGTGTTTCAAAGCTTCCACCGCAAACCAAGC AAGCTTCT ACTGTTGTGGAATCTGTTGATGGCAAAGGGAAAACAGTTCTGAAAGAGCAAACTGTAGTT CCTCCCAC CAAAAAAGTTTCGAGTAAGCATTAAGGAGTTTTTAAGAGTAATAGGCCTTATGACCAACA TATCTCTA AGAAATGTAGCTGTATATGTTATTTAGTCTTGCTTAAAGGTATTTGGATGGTATCATGAA TGTTTTGA TTTATTCGTCGGAGAGACAGATCTTTTGGTGGTTATTAGGCCATTTCTACTGATGGGTGA AGCAATAA ATGTCGTTGTCCTTGCTCTCTGTTTATCTGAGTCTTAATGAATTCTAATGTGTGTCTGCA GGATTTCG TCGTGAGAAAGAAAAGGAGAAGAAGACTTTCGGGGTTGATGGGATGGGTTGTGCCCAGGA AAAAACTA CAGTTCTCCCCAGAAAAATATTGAGTAAGCACTTAGGAAGCTGTGAAGATAGTTAGGCCT TACTTTCA AGATATCTCTTAAAATAATCTGTATATGTTACGTTTTTTTCATTTTGCTGTATTCATTTG GTATCTCG AATGAGATTCTTTATTCCTTGGGTCTCTAAGTTGTTCTAATGATTGTTAGGCAGTTTTTG TGCCTGTG TGACTCTGTTTATCTGTCTAACATATGCAGGTTTTTGTAATGAAATAGAGAAGGATT