Overexpression of YTHDF3 increases the specific productivity of the recombinant protein in CHO cells by promoting the translation process

Author:

Cui Zhao‐ming123,Feng Ying‐ying4,Gao Yan‐ping123,Wang Hai‐tong123,Lu Jiang‐tao1235,Guo Jia‐liang123,Xu Hong‐yan1,Qiu Le‐le6,Wang Tian‐yun236ORCID,Jia Yan‐long123ORCID

Affiliation:

1. School of Pharmacy Xinxiang Medical University Xinxiang Henan China

2. International Joint Research Laboratory for Recombinant Pharmaceutical Protein Expression System of Henan Xinxiang Medical University Xinxiang Henan China

3. Henan Engineering Research Center for Biopharmaceutical Innovation Xinxiang Medical University Xinxiang Henan China

4. The Second Affiliated Hospital of Xinxiang Medical University Xinxiang Henan China

5. State Key Laboratory of Medicinal Chemical Biology Nankai University Tianjin China

6. School of Basic Medicine Xinxiang Medical University Xinxiang Henan China

Abstract

AbstractDue to their high‐quality characteristics, Chinese hamster ovary (CHO) cells have become the most widely used and reliable host cells for the production of recombinant therapeutic proteins in the biomedical field. Previous studies have shown that the m6A reader YTHDF3, which contains the YTH domain, can affect a variety of biological processes by regulating the translation and stability of target mRNAs. This study investigates the effect of YTHDF3 on transgenic CHO cells. The results indicate that stable overexpression of YTHDF3 significantly enhances recombinant protein expression without affecting host cell growth. Transcriptome sequencing indicated that several genes, including translation initiation factor, translation extension factor, and ribosome assembly factor, were upregulated in CHO cells overexpressing YTHDF3. In addition, cycloheximide experiments confirmed that YTHDF3 enhanced transgene expression by promoting translation in CHO cells. In conclusion, the findings in this study provide a novel approach for mammalian cell engineering to increase protein productivity by regulating m6A.

Funder

National Natural Science Foundation of China

Henan Provincial Science and Technology Research Project

Natural Science Foundation of Henan Province

Publisher

Wiley

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