AI Article Synopsis

  • Low-level and unstable transgene expression in CHO cell systems is a common problem, but matrix attachment regions (MARs) can enhance these expression levels, requiring further research for optimization.
  • In a study analyzing two new MARs and MAR-6, one new element, the human CSP-B MAR, was identified as significantly boosting transgene expression in recombinant CHO cells.
  • Bioinformatics suggested that specific elements within the MAR sequences, NFAT and VIBP, may play a role in this enhancement of eGFP expression.

Article Abstract

Low-level and unstable transgene expression are common issues using the CHO cell expression system. Matrix attachment regions (MARs) enhance transgene expression levels, but additional research is needed to improve their function and to determine their mechanism of action. MAR-6 from CHO chromosomes actively mediates high and consistent gene expression. In this study, we compared the effects of two new MARs and MAR-6 on transgene expression in recombinant CHO cells and found one potent MAR element that can significantly increase transgene expression. Two MARs, including the human CSP-B MAR element and DHFR intron MAR element from CHO cells, were cloned and inserted downstream of the poly(A) site in a eukaryotic vector. The constructs were transfected into CHO cells, and the expression levels and stability of eGFP were detected by flow cytometry. The three MAR sequences can be ranked in terms of overall eGFP expression, in decreasing order, as follows: human CSP-B, DHFR intron MAR element and MAR-6. Additionally, as expected, the three MAR-containing vectors showed higher transfection efficiencies and transient transgene expression in comparison with those of the non-MAR-containing vector. Bioinformatics analysis indicated that the NFAT and VIBP elements within MAR sequences may contribute to the enhancement of eGFP expression. In conclusion, the human CSP-B MAR element can improve transgene expression and its effects may be related to the NFAT and VIBP elements.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783848PMC
http://dx.doi.org/10.1111/jcmm.13361DOI Listing

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