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Identification of a potent MAR element from the human genome and assessment of its activity in stably transfected CHO cells
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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783848/ https://www.ncbi.nlm.nih.gov/pubmed/29077269 http://dx.doi.org/10.1111/jcmm.13361 |
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author | Tian, Zheng‐Wei Xu, Dan‐Hua Wang, Tian‐Yun Wang, Xiao‐Yin Xu, Hong‐Yan Zhao, Chun‐Peng Xu, Guang‐Hua |
author_facet | Tian, Zheng‐Wei Xu, Dan‐Hua Wang, Tian‐Yun Wang, Xiao‐Yin Xu, Hong‐Yan Zhao, Chun‐Peng Xu, Guang‐Hua |
author_sort | Tian, Zheng‐Wei |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5783848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57838482018-02-08 Identification of a potent MAR element from the human genome and assessment of its activity in stably transfected CHO cells Tian, Zheng‐Wei Xu, Dan‐Hua Wang, Tian‐Yun Wang, Xiao‐Yin Xu, Hong‐Yan Zhao, Chun‐Peng Xu, Guang‐Hua J Cell Mol Med Original Articles 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. John Wiley and Sons Inc. 2017-10-27 2018-02 /pmc/articles/PMC5783848/ /pubmed/29077269 http://dx.doi.org/10.1111/jcmm.13361 Text en © 2017 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Tian, Zheng‐Wei Xu, Dan‐Hua Wang, Tian‐Yun Wang, Xiao‐Yin Xu, Hong‐Yan Zhao, Chun‐Peng Xu, Guang‐Hua Identification of a potent MAR element from the human genome and assessment of its activity in stably transfected CHO cells |
title | Identification of a potent MAR element from the human genome and assessment of its activity in stably transfected CHO cells |
title_full | Identification of a potent MAR element from the human genome and assessment of its activity in stably transfected CHO cells |
title_fullStr | Identification of a potent MAR element from the human genome and assessment of its activity in stably transfected CHO cells |
title_full_unstemmed | Identification of a potent MAR element from the human genome and assessment of its activity in stably transfected CHO cells |
title_short | Identification of a potent MAR element from the human genome and assessment of its activity in stably transfected CHO cells |
title_sort | identification of a potent mar element from the human genome and assessment of its activity in stably transfected cho cells |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783848/ https://www.ncbi.nlm.nih.gov/pubmed/29077269 http://dx.doi.org/10.1111/jcmm.13361 |
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