Exploring the Potential Application of Short Non-Coding RNA-Based Genetic Circuits in Chinese Hamster Ovary Cells

被引:7
|
作者
Curell, Ricardo Valdes-Bango [1 ]
Barron, Niall [2 ,3 ]
机构
[1] Dublin City Univ, Natl Inst Cellular Biotechnol, Dublin, Ireland
[2] Natl Inst Bioproc Res & Training, Fosters Ave, Dublin, Ireland
[3] Univ Coll Dublin, Dublin, Ireland
基金
欧盟地平线“2020”;
关键词
cellular engineering; CHO cells; genetic circuits; miRNA; protein expression control; RNA interference; synthetic biology; MAMMALIAN-CELLS; PROTEIN-PRODUCTION; CHO-CELLS; TRANSGENE EXPRESSION; RECOMBINANT PROTEIN; ENDOGENOUS MICRORNA; MESSENGER-RNAS; IDENTIFICATION; DESIGN; DIFFERENTIATION;
D O I
10.1002/biot.201700220
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The majority of cell engineering for recombinant protein production to date has relied on traditional genetic engineering strategies, such as gene overexpression and gene knock-outs, to substantially improve the production capabilities of Chinese Hamster Ovary (CHO) cells. However, further improvements in cellular productivity or control over product quality is likely to require more sophisticated rational approaches to coordinate and balance cellular pathways. For these strategies to be implemented, novel molecular tools need to be developed to facilitate more refined control of gene expression. Multiple gene control strategies are developed over the last decades in the field of synthetic biology, including DNA and RNA-based systems, which allows tight and timely control over gene expression. microRNAs has received a lot of attention over the last decade in the CHO field and are used to engineer and improve CHO cells. In this review we focus on microRNA-based gene control systems and discuss their potential use as tools rather than targets in order to gain better control over gene expression.
引用
收藏
页数:8
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