1. FIELD OF THE INVENTION The present invention relates to a polynucleotide sequence and an expression vector for a eukaryotic cell to express a protein of interest. Furthermore, the present invention relates to an expression vector that prolongs life of cell line.

2. DESCRIPTION OF THE RELATED ART

Recombinant technology has been used to clone, express and purify several proteins of therapeutic or other economic value. Use of Eukaryotic host cells to express large quantity of recombinant proteins in large amounts has become increasingly important because of the ability of Eukaryotic cells to express the protein of interest in desired conformation. Method to improve protein expression often includes increasing gene dosage or copies, or by adding genetic elements that prolong life of cells. Various factors affect the ability of the expression vector to express the protein during fermentation. These include selection marker gene used for selection of vector containing cells from other cells, Orientation of the genes coding for product of interest, strength of the promoter linked to the gene for protein of the interest, the sequence of the 5' untranslated and the translation initiation region, the efficiency of the 3' untranslated region to polyadenylate and terminate transcription, the insertion site of the randomly integrated recombinant gene in the host chromosome, and the number of integrated copies of the gene that is being expressed. In spite of the plethora of available vectors, production of robust cell lines producing the polypeptide/protein at high concentration in a consistent manner is still challenging. Several other factors can influence the yield for expression of recombinant protein in mammalian cells, some of them are protein to be expressed, Media components, Host cell lines used, etc.

Other problem associated with industrial production of recombinant proteins using eukaryotic cells is related to stress conditions incurred by cells during the late stages of fermentation. During the late phases of the fermentation the number of cells are more as compared to early phases of fermentation. Hence, the protein of interest is produced at much faster rate. During the late phase of the fermentation, the cells are exposed to stress conditions such as high temperature, high osmotic pressure, metabolic inhibition, presence of heavy metals, viral infection, etc. These factors negatively affect the fermentation process and expression of the protein of interest by increasing the rate of cell death. The increase in cell death results in decrease in time of the fermentation cycles per batch. This result in decrease in overall yield of the protein produced per batch. This leads to increases in duration of the fermentation cycle to improve the overall yield of protein of interest and thus increasing the cost of production.

The patent application US7935808 discloses REVE sequences which may comprise one or more matrix attachment region (MAR) sequences. MAR sequences may occur in clusters within a rEVE sequence, including in clusters at the 5' and/or 3' terminal regions of a rEVE sequence. It further discloses Dihyrofolate reductase for higher survivability and/or higher growth rate. The patent discloses use of Heat shock protein (HSP) with other elements like MAR, gene of interest to achieve stable cell. However, the incorporation of three genes i.e. HSP gene , MAR sequence and Gene for protein, into its genome at a stable location is not disclosed. Despite significant progress in improving the yield from these cells, the process to the selection, identification, and maintenance of high-producing cell lines remains cumbersome, time consuming, and often of uncertain outcome. Thus, there is a need in the art to design improved expression vectors useful for protein expression in mammalian cells which can overcome the deficiencies of the known methods and thus improve the expression of the vectors to yield highly stable and viable cell lines. In the present invention, the vectors so designed will provide an efficient generation of stable cell lines expressing the product of interest at desired levels. The vector generates a high expression stable cells lines with higher viability and stability and yet reduces the total time of fermentation by reducing the number of fermentation cycles and overcomes the drawbacks presented by the prior art.

SUMMARY OF THE INVENTION

Surprisingly, the inventors have developed a polynucleotide sequence for a eukaryotic cell which for instance, generates high expression stable cell lines with higher viability and stability. The polynucleotide sequence comprises:

at least one promoter;

at least one gene encoding a stress resistance protein;

at least one gene encoding a selection marker;

at least one gene encoding an expression protein ; and,

a transcription terminator, all of which are operably connected to each other

Also, surprisingly the inventors have discovered an expression vector for a eukaryotic cell comprising: at least one promoter;

at least one gene encoding a stress resistance protein;

at least one gene encoding a selection marker;

at least one gene encoding an expression protein ; and,

a transcription terminator, all of which are operably connected to each other.

Furthermore, the expression vector for a eukaryotic cell demonstrates excellent protein expression, high stability and viability and can be effectively used for the production of protein of interest.

The present invention relates to an expression vector comprising polynucleotide sequence of SEQ ID. NO: 1. The present invention relates to a host cell comprising the expression vector. Further, surprisingly the inventors of the application have discovered a method of producing a stable and viable cell lines comprising, for the expression of a gene of interest in a host cell, the method comprises transfecting a host cell with the expression vector and, culturing the transfected host cell

Quite advantageously, the method of producing cell line comprising the expression vector can be used efficiently for production of protein of interest with high expression, stability and longer viability of the strain containing the expression vector and it still further expedites the production of protein of interest by reducing the number of fermentation cycles

BRIEF DESCRIPTION OF THE DRAWINGS

For a more complete understanding of the invention, reference should now be made to the embodiment illustrated in greater detail in the accompanying drawing and described below by way of examples of the invention. FIGURE 1 : illustrates the fragments of the expression vector pBGMESV in accordance with the embodiment of the invention.

FIGURE 2: illustrates the yield achieved for transient transfection of CHO DHFR ^" cells with pBGMESV- EPO in accordance with an embodiment of the invention and pBUD-EPO expression vectors.

FIGURE 3: illustrates hCMV promoter linked to HSP 27 gene which is connected to IRES linked DHFR gene having thymidine kinase Polyadenylation sequence at 5' end in accordance with the embodiment of the invention. FIGURE 4a and FIGURE 4b: illustrates comparison between the cell count and cell viability of the mammalian cells in pBGMESV vector and in a vector without HSP and MAR

DETAILED DESCRIPTION OF THE INVENTION

As required, detailed embodiments of the present invention are disclosed herein; however, it is to be understood that the disclosed embodiments are merely exemplary of the invention, which can be embodied in various forms. Therefore, specific structural and functional details disclosed herein are not to be interpreted as limiting, but merely as a basis for the claims and as a representative basis for teaching one skilled in the art to variously employ the present invention in virtually any appropriately detailed structure. Further, the terms and phrases used herein are not intended to be limiting but rather to provide an understandable description of the invention.

The terms "a" or "an", as used herein, are defined as one or more than one. The term "plurality", as used herein, is defined as two or more than two. The term "another", as used herein, is defined as at least a second or more. The terms "including" and/or "having", as used herein, are defined as comprising (i.e., open language).

The present invention provides an expression vector for a eukaryotic cell that demonstrates excellent protein expression, high stability and viability and can be effectively used for the production of protein of interest. Such vectors are referred to herein as plasmid BioGenomics Mammaliam Expression Super Vector (pBGMESV).

As described herein, the abbreviation MTX refers to Methotrexate. As described herein, the abbreviation "DHFR" refers to Dihydrofolate reductase. As described herein, the abbreviation "CHO" refers to chicken lysozyme enzyme. As described herein, the abbreviation "HRP-Conjugated antibody" refers to Horseradish Peroxidase- Conjugated antibody. As described herein, the abbreviation "hCMV promoter" refers to Human cytomegalovirus promoter. As described herein, the abbreviation "pBUD-EPO" refers to pBUD-Erythropoietin (INVITROGEN, 4595 bp), As described herein, the abbreviation "HSP" refers to Heat shock proteins. As described herein, the abbreviation "MAR" refers to Matrix attachment region. As described herein, the abbreviation "IRES" refers to internal ribosome entry site

Vector Deposition The vector pBGMESV is deposited for the patent purposes under Budapest Treaty at the MTCC (Microbial Type of Culture Collection) Chandigarh, India. The deposit was made on 20th January, 2011 and accorded deposit number for the same. The deposit number for vector pBGMESV is MTCC 5682. The sequence was characterised using DNA Sequencer. . The invention relates to, a polynucleotide sequence for a eukaryotic cell which comprises:

at least one promoter;

at least one gene encoding a stress resistance protein;

at least one gene encoding a selection marker;

at least one gene encoding an expression protein ; and,

a transcription terminator, all of which are operably connected to each other

According to an embodiment, the polynucleotide comprises an internal ribosome entry site (IRES) linked to the gene encoding the selection marker. According to an embodiment, the polynucleotide sequence wherein the internal ribosome entry site (IRES) can be Picornavirus IRES, Aphthovirus IRES, Hepatitis A IRES, Hepatitis C IRES, Pestivirus IRES, Cripavirus IRES, Kaposi's sarcoma-associated herpesvirus IRES or combination thereof.

Other IRES sequences of the polynucleotide sequence known to those skilled in the art can also be utilized for expression of the gene for selection marker in accordance with the present invention. According to an embodiment, the polynucleotide sequence wherein the polynucleotide comprises at least one matrix attachment region.

According to an embodiment, MAR of the polynucleotide sequence can be Humans, Xenopus, mouse, or any other plant and animal sources or fragments thereof

In a preferred embodiment, the MAR of the polynucleotide sequence is chicken lysozyme MAR element.

According to another embodiment, MAR of the polynucleotide sequences are identified, isolated, and cloned using a variety of techniques well known to those of ordinary skilled in the art.

According to an embodiment, the stress resistance protein of the polynucleotide sequence can be one of HSP 70, HSP 90, HSP 27, or a combination thereof. In a preferred embodiment, the stress resistance protein of the polynucleotide sequence is HSP27.

According to an embodiment, the selection marker of the polynucleotide sequence is optionally linked to the internal ribosome entry site. According to an embodiment, the selection marker of the polynucleotide sequence can be a glutamine synthatase, dihydrofolate reductase, antibiotic resistance gene, auxotrophic marker, or combination thereof.

In a preferred embodiment, the selection marker of the polynucleotide sequence is dihydrofolate reductase.

According to another embodiment, the promoter of the polynucleotide sequence can be a PEF 1 alpha promoter, a hCMV promoter, or a HSP promoter. According to yet another embodiment, the transcription terminator of the polynucleotide sequence is bovine growth hormone polyadenylation signal.

According to another embodiment, the gene encoding an expression protein of the polynucleotide sequence encodes insulin and insulin analogues, trypsin, carboxypeptidase, DNA ligase, interferons and their conjugates, filgrastim and its conjugates, polymerases, bevacizumab, trastuzumab, infliximab, rituximab, adalimumab, erythropoietin, etanercept, ranibizumab, transferrins, kinases, growth hormones, or albumin or any other recombinant protein of therapeutic or non-therapeutic significance. .

According to an embodiment, enhancer elements of the polynucleotide sequence are optionally included in one or more of the vectors of the invention. According to an embodiment, an expression vector for a eukaryotic cell comprising: at least one promoter;

at least one gene encoding a stress resistance protein;

at least one gene encoding a selection marker;

at least one gene encoding an expression protein ; and,

a transcription terminator, all of which are operably connected to each other.

According to an embodiment, an expression vector for an animal cells comprising:

at least one promoter;

at least one gene encoding a stress resistance protein;

at least one gene encoding a selection marker;

at least one gene encoding an expression protein ; and,

a transcription terminator, all of which are operably connected to each other.

According to an embodiment, the expression vector comprises an internal ribosome entry site (IRES) linked to the gene encoding the selection marker.

Other IRES sequences of the expression vector known to those skilled in the art can also be utilized for expression of the gene for selection marker in accordance with the present invention.

According to an embodiment, the expression vector comprises the Internal ribosome entry site (IRES) can be Picornavirus IRES, Aphthovirus IRES , Hepatitis A IRES, Hepatitis C IRES, Pestivirus IRES, Cripavirus IRES, Kaposi's sarcoma-associated herpesvirus IRES, or combination thereof.

According to an embodiment, the expression vector comprises MAR.

According to an embodiment, MAR of the expression vector can be humans, Xenopus, mouse, or any other plant and aninial sources or fragments thereof.

In a preferred embodiment, the MAR of the expression vector can be chicken lysozyme MAR element.

According to another embodiment, MAR of the expression vectors are identified, isolated, and cloned using a variety of techniques well known to those of ordinary skilled in the art.

According to an embodiment, the stress resistance protein of the expression vector can be HSP 70, HSP 90, HSP 27, or combination thereof.

In a preferred embodiment, the stress resistance protein of the expression vector is HSP27.

According to an embodiment, the selection marker of the expression vector is linked to the internal ribosome entry site. According to an embodiment, the selection marker of the expression vector is can be glutamine synthatase, dihydrofolate reductase, antibiotic resistance gene, auxotrophic marker or combination thereof. In a preferred embodiment, the selection marker of the expression vector is dihydrofolate reductase.

According to another embodiment, the promoter of the expression vector can be a PEF 1 alpha promoter, hCMV promoter, or an HSP promoter. According to yet another embodiment, the transcription terminator of the expression vector is bovine growth hormone polyadenylation signal.

According to another embodiment, the gene encoding an expression protein of the expression vector encodes insulin and insulin analogues, trypsin, carboxypeptidase, DNA ligase, interferons and their cojugates, filgrastim and its conjugates, polymerases, bevacizumab, trastuzumab, infliximab, rituximab, adalimumab, erythropoietin, etanercept, ranibizumab, transferrins, kinases, growth hormones, or albumin.

According to an embodiment, an expression vector is comprising a polynucleotide sequence comprising of the nucleotide base sequence of SEQ ID NO: 1. The polynucleotide sequence has 9516 base pairs (Figure 1 ) According to an embodiment, the expression vector pBGMESV comprises:

at least one promoter;

at least one gene encoding a stress resistance protein;

at least one gene encoding a selection marker;

at least one gene encoding an expression protein ; and,

a transcription terminator, all of which are operably connected to each other.

According to an embodiment, the expression vector pBGMESV further comprises an internal ribosome entry site (IRES) linked to the gene encoding the selection marker.

According to an embodiment, the expression vector pBGMESV, comprises at least one matrix attachment region

According to an embodiment, enhancer elements of the expression vector are optionally included in one or more of the vectors of the present invention.

According to an embodiment, a method of transforming one or more eukaryotic cells comprising at least one gene encoding a matrix attachment region, at least one gene encoding a stress resistance protein, at least one gene encoding an expression protein.

According to another embodiment, the genes can be present in a plurality of vectors. According to an embodiment, after the transformation of cell cultures, higher titre clones, are selected by known methods under standard conditions.

According to an embodiment, FIGURE 1 illustrates the fragments of the expression vector pBGMESV. According to an embodiment, FIGURE 2 illustrates the yield achieved for transient transfection of CHO DHFR ^" cells with pBGMESV-EPO and pBUD-EPO expression vectors.

According to an embodiment, FIGURE 3 illustrates hCMV promoter linked to HSP 27 gene which is connected to IRES linked DHFR gene having thymidine kinase Polyadenylation sequence at 5' end.

According to an embodiment, FIGURE 4a and 4b illustrates comparison of the cell count and cell viability of the mammalian cells in pBGMESV vector and in a vector without HSP and MAR.

According to another embodiment, a host cell comprises of the polynucleotide sequence of SEQ ID NO: 1.

According to another embodiment, a host cell comprises the expression vector.

According to an embodiment, the eukaryotic cell type can be. stem cells, embryonic stem cells, COS, BHK21 , NIH3T3, HeLa, C2C12, CHO-K1 , CHO DG44, DXB11 , CHO-S, NSO, BHK, Vera, Per C6, HEK293 cells, cancer cells and primary differentiated or undifferentiated cells.

Other suitable host cells known to those skilled in the art can also be used in accordance with the present invention.

According to an embodiment, a method of producing stable and viable cell lines for the expression of a gene of interest in a host cell, the method comprising: transfecting a host cell with the expression vector; and, culturing the transfected host cell. According to an embodiment, the cell lines are produced in accordance with the method of producing the cell lines.

In respect of the features described above in relation to one or more aspects or embodiments of the invention, it should be understood that any two or more of the features may be combined in any appropriate combination.

The polynucleotide has been found to be advantageous over prior art vectors in several ways. Stable cell lines using expression vectors comprising the polynucleotide sequence have been obtained within a very short period of time as compared to the prior art vectors which do not include the polynucleotide sequence. Furthermore, the polynucleotide also enables the gene to be insulated from repressive effects of neighbouring chromatin or regulatory elements. Surprisingly, they also increase the overall expression of the transgene the polynucleotide improves the probability of high expressing cell line and increase the stability and viability of expressed product.

The examples given below in a non-limiting manner will make it possible to better understand the invention:

Examples

Example 1 : pBGMESV

The vector pBGMESV (FIGURE 1 ) contains the Chicken lysozyme Matrix attachment region upstream of PEF-1 alpha promoter, PEF-1 alpha promoter is operably linked to multiple cloning site followed by BGH polyadenylation sequence. Gene for HSP 27 is linked to hCMV promoter. The gene for DHFR selection marker linked to IRES wherein the thymidine kinase polyadenylation sequence is linked to 5' end of DHFR gene. The gene for HSP27 and DHFR are arranged in a manner which allows the transcription of a single mRNA containing the sequence of HSP27 and DHFR. The mRNA also contains sequence for the internal ribosome entry site which allows the initiation of the translation of the DHFR protein. The complete sequence of gene coding for hCMV promoter is linked to HSP 27 gene which is connected to IRES linked DHFR gene having thymidine kinase Polyadenylation sequence at 5' end. The thymidine kinase polyadenylation sequence carries out the termination of transcription. The vector also contains bacterial selection marker i.e. gene for Ampicillin resistance for selection of transformants in bacteria more specifically in E.coli. The vector also contains gene acting as origin of replication in bacteria. The hCMV promoter is operably linked to gene for HSP. Gene for DHFR is operably linked to EMCV IRES at 3' end and TK polyadenylation sequence at 5' end. The gene of interest is cloned in the multiple cloning sites. The size of pBGMESV is 9516 bp.

Example 2: Comparison of expression efficiencies of pBUD-EPO and pBGMESV-EPO by transient transfection

Host cells i.e suspension adapted CHO-DHFR ^" (created from adaptation of CHO-DHFR ^" adherant.cell lines provided by NCCS, Pune, India) were maintained in complete growth medium (CHO EXCELL- DHFR medium (Invitrogen) supplemented with 100 μΜ Hypoxanthine, 16 μΜ Thymidine and 6mM glutamine) at a temperature of 37°C and in an atmosphere of 5% C0 ₂ . Cells were seeded at the density of 0.5 X10 ⁶ /ml in a 6-well plate, 24 hours prior to electroporation Transfection was carried out using Neon Eletroporator (Invitrogen). Both the vectors were transfected into CHO DHFR ^~ cells and expression level was studied. 3pg of vector DNA was added to 100μΙ media containing 1 X 10 ^s cells in electroporation cuvette and electroporated at 1600 Volts with 3 pulses expecting an electroporation time of around 10 millisec. Following electroporation, 100μΙ volume of cells was transferred to 6-well plate comprising 2 ml medium. The plate was then gently swirled to ensure proper mixing and incubated for 48 hours at 37°C in 5% C0 ₂ The spent media was collected from the 6 well-plate at 48 hours. The expression of EPO was analyzed by EPO Immunoassay kit (R & D Systems).

Example 3 Analysis of expression yields achieved using EPO Immunoassay kit (R&D Systems).

Supernatants from all wells of 6 well plate containing transformed cells growing for 48 hours was collected and diluted appropriately with specimen diluent. Standard dilutions were prepared between the ranges of 0-200 mlU. 100μΙ of assay diluent was added to each well of micro titer plate. 100 pi of diluted samples were added to the wells. EPO standards provided in the kit were added to standard lane as follows: 200 mlU/ml, 100 mlU/ml, 50 mlU/ml, 20 mlU/ml, 5 mlU/ml, 2.5 mlU/ml, and 0 mlU/ml. Samples were incubated for 2 hours to allow antigen-antibody binding to take place. The plates were tapped to remove the unbound antibody. 100 pi of HRP-Conjugated antibody (Polyclonal rabbit antibody against recombinant human-EPO) was added to all the micro titer wells and further incubated at room temperature for 2 hours followed by washing (three times) using 300 μΙ of 1X wash buffer provided in kit.100 μΙ of each colour reagent A and B were added to each well and incubated in dark for approximately 20-25 minutes. The reaction was stopped by addition of 100 μΙ of 2N sulfuric acid. Absorbance was measured in ELISA reader (Fluostar Galaxy) at 450nm. Standard graph of O.D (450 nm) Vs. Concentration (ng/ml) was plotted and values of unknown samples were derived from the equation. FIGURE 2 depicts representative data for yield achieved for transient transfection of CHO DHFR ^" cells with pBGMESV-EPO and pBUD-EPO expression vectors. The highest expression was obtained with pBGMESV-EPO was 16 μg/ml/day whereas pBUD-EPO showed expression level of 745 ng/ml/day.

Example 4: Stable transfection of suspension adapted CHO DHFR ^" cells with pBGMESV-EPO construct Suspension adapted CHO DHFR ^" (created from adaptation of CHO-DHFR ^' adherent cell lines provided by NCCS, Pune, India) cells were cultured in Hypoxanthine-Thymidine (HT) lacking EXCELL- DHFR medium (Invitrogen) comprising of 6 mM glutamine. Media change was given to the cells 24 hours prior to electroporation. 3pg DNA was added to 100μΙ media containing 1 X 10 ⁶ cells in electroporation cuvette and electroporation was carried out at 1600 Volts with 3 pulses of an electroporation time of around 10 msec. Following electroporation, 00μΙ medium containing 1 X 10 ⁶ cells was transferred to 6-well plate comprising 2 ml medium. The plate was incubated for 48 hours at 37°C in 5% C0 _2. Cell count was performed using Trypan blue dye exclusion method, 48 hours post electroporation. Based on the cell count, the medium was diluted to perform single cell cloning. 20 nM MTX pressure was maintained in the diluted culture. The plates were observed on a standard inverted microscope for confirming the single cell cloning. Transfectants were further incubated for 25 days at 37°C in 5 % C0 ₂ for colony formation. Individual colonies were analyzed for EPO production using EPO Immunoassay kit (R&D Systems) as mentioned in example 3.

Example 5: Clone Selection and gene amplification Clones showing High expression were selected and were subjected to methotrexate (MTX) - based gene amplification process. 20nM MTX was added to the selection media (CHO Excell DHFR Medium) lacking Hypoxanthine-Thymidine and supplemented with 6mM glutamine. Media was changed after every three days. The cells were grown in same concentration of MTX for about 15-20 days. Populations that reached normal growth at chosen level of drug were used for next round of selection. Expression of each clone was analyzed after every stage of increasing concentration of MTX. All the selected clones were subjected to sequential increasing MTX concentrations of 20nM, 100nM, 200nM, 400nM and finally, 2μΜ MTX. The results were expressed as total amount of EPO protein secreted/10 ⁵ cells/ml. High expressing clones were expanded and frozen down as master cell bank for commercial production of EPO.

Example 6: Evaluation of nutritional stress of cell lines (comparison of CHO-S Relipofection HSP 27 and Plain CHO-S HSP 27)

A comparative study between a mammalian cell clone pBGMESV vector and a vector without HSP gene and MAR gene was conducted to analyse the impact of HSP gene in presence of MAR gene in the vector. The Culture conditions were maintained for both the culture flasks similar to described in example 4. Experiment was conducted in batch fermentation mode, to impart nutritional stress on the culture flasks. Mammalian cells of pBGMESV vector and a vector without HSP and MAR genes were seeded at 0.3 million cells/ml density in separate 125ml shake flasks containing 10ml of complete, chemically defined medium. After seeding, 0.2ml of sample was taken out for performing cell count and cell viability with the help of Hemocytometer and Trypan blue dye exclusion method. Results were noted in the observation tables as Day zero readings and the culture flasks were incubated on a shaker maintained at 130 rpm in the C02 incubator maintained at 37°C temperature and 8% C02. Post day-2, cell count and cell viability were analysed after every 24hrs, till the culture viability reached 0% and readings were noted in the observation tables. Glucose concentration in both the culture flasks was analysed periodically with the help of glucometer. The cell count and cell viability of the mammalian cells in pBGMESV vector and a vector without HSP and MAR are depicted in FIGURE 4a and 4b. Based on the above experiment, culture with HSP and MAR sustained viability for 24hrs more than the culture without HSP. It was observed that increase in viable cell density of culture with HSP and MAR was observed till day-5, while there was no significant increase in viable cell density of non HSP culture. Lack of glucose as seen in FIGURE 4a and 4b, post day-5 suggested that the culture is deprived of nutrition, thus it can be inferred that the culture is under nutritional stress pBGMESV vector with HSP and MAR could sustain viability for 24 hrs more than the culture without MAR and HSP due to their ability to combat nutritional stress. Similarly increase in viable cell density was observed in culture with HSP and MAR while with similar culture conditions non HSP and MAR cells failed to divide post lack of glucose. Hence it can be concluded that HSP along with MAR sequence in pBGMESV vector makes the culture stress resistant.

During heat shock, both constitutive and stress-inducible HSPs bind to and inhibit irreversible aggregation of denatured protein and facilitate their refolding once normal cellular conditions are re-established. The dual role of HSP's in both normal and stressed cells, evidently requires the existence of complex regulatory processes which ensure that the correct expression pattern is produced. MAR helps to generate and maintain an open chromatin domain that is favourable to transcription and may also facilitate the integration of several copies of the transgene. Thus, incorporating HSP in presence of MAR gene in a pBGMESV vector leads to an elongated fermentation cycles at industrial scale resulting to higher production of recombinant proteins.

From the foregoing, it will be observed that numerous modifications and variations can be effectuated without departing from the true spirit and scope of the novel concepts of the present invention. It is to be understood that no limitation with respect to the specific embodiments illustrated is intended or should be inferred.