Stabilizing and Anti-Repressor Elements Effectively Increases Transgene Expression in Transfected CHO Cells.
Autor: | Li Q; School of Basic Medicine, Xinxiang Medical University, Xinxiang, China.; International Joint Research Laboratory for Recombinant Pharmaceutical Protein Expression System of Henan, Xinxiang Medical University, Xinxiang, China., Yan RF; School of Basic Medicine, Xinxiang Medical University, Xinxiang, China., Yang YX; International Joint Research Laboratory for Recombinant Pharmaceutical Protein Expression System of Henan, Xinxiang Medical University, Xinxiang, China., Mi CL; School of Basic Medicine, Xinxiang Medical University, Xinxiang, China.; International Joint Research Laboratory for Recombinant Pharmaceutical Protein Expression System of Henan, Xinxiang Medical University, Xinxiang, China., Jia YL; International Joint Research Laboratory for Recombinant Pharmaceutical Protein Expression System of Henan, Xinxiang Medical University, Xinxiang, China., Wang TY; School of Basic Medicine, Xinxiang Medical University, Xinxiang, China.; International Joint Research Laboratory for Recombinant Pharmaceutical Protein Expression System of Henan, Xinxiang Medical University, Xinxiang, China. |
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Jazyk: | angličtina |
Zdroj: | Frontiers in bioengineering and biotechnology [Front Bioeng Biotechnol] 2022 May 26; Vol. 10, pp. 840600. Date of Electronic Publication: 2022 May 26 (Print Publication: 2022). |
DOI: | 10.3389/fbioe.2022.840600 |
Abstrakt: | Chinese hamster ovary (CHO) cells are currently the most widely used host cells for recombinant therapeutic protein (RTP) production. Currently, the RTP yields need to increase further to meet the market needs and reduce costs. In this study, three stabilizing and anti-repressor (SAR) elements from the human genome were selected, including human SAR7, SAR40, and SAR44 elements. SAR elements were cloned upstream of the promoter in the eukaryotic vector, followed by transfection into CHO cells, and were screened under G418 pressure. Flow cytometry was used to detect enhanced green fluorescent protein (eGFP) expression levels. The gene copy numbers and mRNA expression levels were determined through quantitative real-time PCR. Furthermore, the effect of the stronger SAR elements on adalimumab was investigated. The results showed that transgene expression levels in the SAR-containing vectors were higher than that of the control vector, and SAR7 and SAR40 significantly increased and maintained the long-term expression of the transgene in CHO cells. In addition, the transgene expression level increase was related with gene copy numbers and mRNA expression levels. Collectively, SAR elements can enhance the transgene expression and maintain the long-term expression of a transgene in transfected CHO cells, which may be used to increase recombinant protein production in CHO cells. Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. (Copyright © 2022 Li, Yan, Yang, Mi, Jia and Wang.) |
Databáze: | MEDLINE |
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