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Attachment expression vector of cells of human and other mammals, expression system, preparation method and application

An expression vector and mammalian technology, applied in the field of genetic engineering and gene therapy, can solve the problems of low expression level, widening gap, unstable expression, etc.

Active Publication Date: 2017-03-15
XINXIANG MEDICAL UNIV
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  • Abstract
  • Description
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Problems solved by technology

Publication number CN102703503A discloses a human and mammalian episomal expression vector, which is inserted with a synthetic β-interferon characteristic MAR sequence (387bp, specifically composed of human β-interferon MAR sequence 2200bp and human β-bead The 2150bp characteristic elements of the protein MAR sequence are cut and spliced), which can mediate the expression of foreign genes in mammalian cells, and because the foreign genes are attached rather than integrated into the host chromosome, it can also overcome the integration effect of traditional vectors However, the study also found that the transgene expression driven by the expression vector had defects such as low copy number, unstable expression and low expression level, which led to a widening gap between the research itself and clinical application

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  • Attachment expression vector of cells of human and other mammals, expression system, preparation method and application
  • Attachment expression vector of cells of human and other mammals, expression system, preparation method and application
  • Attachment expression vector of cells of human and other mammals, expression system, preparation method and application

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Experimental program
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Effect test

Embodiment 1

[0041] The construction of the expression vector pMAR-InE, the specific steps are as follows:

[0042] 1) using human peripheral blood genomic DNA as a template, using primers to perform PCR amplification on E1 / E2 to obtain MAR fragments;

[0043] The primer pair E1 / E2 is:

[0044] E1: 5′-ATC GGTACC TATCCATAGCTGATTGGTCT-3';

[0045] E2: 5′-TGA GGATCC CTATCAAGATATTTAAAGAAA-3′;

[0046] The amplification reaction system is: 10×PCR buffer 2.5μL, 25μmol / L dNTP 2.0μL, 5U / μL Taq enzyme 0.5μL, 100ng / μL template DNA 1.0μL, 10μmol / L primer E1 / E2 each 1.0μL, ddH 2 O 17.0 μL, a total of 25 μL;

[0047] The reaction program of the amplification is: 95°C for 3min, 94°C for 40s, 56°C for 30s, 72°C for 40s, 30 cycles, 72°C for 3min;

[0048] 2) Digest the above MAR fragment and pEGFP-C1 plasmid DNA with KpnⅠ and BamHI enzymes, recover the digested MAR fragment and pEGFP-C1 linear plasmid DNA from the gel, transform E.coli JM109 strain competent cells after ligation, and identify , to o...

Embodiment 2

[0053] The construction of the expression vector pMAR-InD, except that the primer pair D1 / D2 is used for PCR amplification, other operations are basically the same as in Example 1;

[0054] Primer pair D1 / D2 is:

[0055] D1: 5′-ATC GGTACC TACCCCATGGGCTTCCTCCC-3′;

[0056] D2: 5′-TGA GGATCC TCTCAATTTTGCTATGAACC-3'.

Embodiment 3

[0058] The construction of the expression vector pMAR-InC, except that the primer pair C1 / C2 is used for PCR amplification, other operations are basically the same as in Example 1;

[0059] Primer pair C1 / C2 is:

[0060] C1: 5′-ATC GGTACC CATGCCATCATGACTTCAGT-3';

[0061] C2: 5′-TGA GGATCC TATTTTTGATGACCTTGACA-3'.

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Abstract

The invention discloses an attachment expression vector of cells of human and other mammals, an expression system, a preparation method and application and belongs to the technical fields of genetic engineering and gene therapy. A segment beta-interferon MAR (matrix attachment region) sequence (or an nucleotide sequence which is 95 percent homologous with the sequence or more), which is shown as SEQ ID NO: 1, SEQ ID NO: 2 or SEQ ID NO: 3, is inserted into the attachment expression vector; compared with an expression vector containing a whole-length MAR sequence or a 387bp MAR sequence, the vector can efficiently, lastingly and stably express exogenous target genes; especially, the expression of the vector containing an E-segment MAR sequence is optimum and the expression vector can be used for the gene therapy. In the vector, a multiple cloning site where the segment MAR sequence is inserted into the vector is located at the downstream of eGFP (enhanced Green Fluorescent Protein); on one hand, transgene silencing can be overcome; on the other hand, an expression level of a target protein can be improved and the effectiveness of subsequent monoclonal cell strain screening are improved.

Description

technical field [0001] The invention relates to a human and other mammalian cell attachment expression vector, and also relates to the expression system, preparation method and application of the attachment expression vector, belonging to the technical field of genetic engineering and gene therapy. Background technique [0002] Gene therapy is to introduce normal and functional genes into target cells to correct or compensate for the defects produced by disease-causing genes, so as to achieve the purpose of treating diseases. Effective gene therapy depends on the efficient and stable expression of foreign genes in recipients, and depends to a large extent on the vector system used. Vectors are divided into viral vectors and plasmid vectors due to different ways of entering host cells. At present, viral vectors with high transfection efficiency are the most used, such as adenovirus and retroviral vectors. However, after the viral vector is transfected into the host cell, it ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N15/85
CPCC12N15/85C12N2800/107
Inventor 王小引王天云张玺王俐李琴王芳张俊河林艳付笑笑
Owner XINXIANG MEDICAL UNIV
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