Wang You, Li Chunying, Khan Md Rezaul Islam, Wang Yushu, Ruan Yunfeng, Zhao Bin, Zhang Bo, Ma Xiaopan, Zhang Kaisi, Zhao Xiwen, Ye Guanhao, Guo Xizhi, Feng Guoyin, He Lin, Ma Gang
Bio-X institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai 200240, PR China.
2011 SJTU-BioX-Shanghai Team for The International Genetically Engineered Machine Competition (iGEM), Shanghai Jiao Tong University, Shanghai, PR China.
Sci Rep. 2016 Feb 8;6:20608. doi: 10.1038/srep20608.
Rare codons generally arrest translation due to rarity of their cognate tRNAs. This property of rare codons can be utilized to regulate protein expression. In this study, a linear relationship was found between expression levels of genes and copy numbers of rare codons inserted within them. Based on this discovery, we constructed a molecular device in Escherichia coli using the rare codon AGG, its cognate tRNA (tRNA(Arg) (CCU)), modified tRNA(Asp) (GUC → CCU), and truncated aspartyl-tRNA synthetase (TDRS) to switch the expression of reporter genes on or off as well as to precisely regulate their expression to various intermediate levels. To underscore the applicability of our work, we used the rare codon device to alter the expression levels of four genes of the fatty acid synthesis II (FASII) pathway (i.e. fabZ, fabG, fabI, and tesA') in E. coli to optimize steady-state kinetics, which produced nearly two-fold increase in fatty acid yield. Thus, the proposed method has potential applications in regulating target protein expression at desired levels and optimizing metabolic pathways by precisely tuning in vivo molar ratio of relevant enzymes.
稀有密码子通常因其同源tRNA的稀缺性而导致翻译终止。稀有密码子的这一特性可用于调控蛋白质表达。在本研究中,发现基因的表达水平与其中插入的稀有密码子拷贝数之间存在线性关系。基于这一发现,我们在大肠杆菌中构建了一种分子装置,利用稀有密码子AGG、其同源tRNA(tRNA(Arg) (CCU))、修饰的tRNA(Asp) (GUC → CCU)和截短的天冬氨酰-tRNA合成酶(TDRS)来开启或关闭报告基因的表达,并将其表达精确调控至各种中间水平。为强调我们工作的适用性,我们使用稀有密码子装置改变大肠杆菌中脂肪酸合成II(FASII)途径的四个基因(即fabZ、fabG、fabI和tesA')的表达水平,以优化稳态动力学,这使脂肪酸产量提高了近两倍。因此,所提出的方法在将靶蛋白表达调控至所需水平以及通过精确调节体内相关酶的摩尔比来优化代谢途径方面具有潜在应用。