遗传密码
终止密码子
基因
遗传学
密码子使用偏好性
氨基酸
生物
翻译(生物学)
基因组
大肠杆菌
释放系数
噬菌体
计算生物学
转移RNA
核糖核酸
信使核糖核酸
作者
J. G. Lajoie,Sriram Kosuri,Joshua A. Mosberg,Christopher Gregg,Di Zhang,George M. Church
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2013-10-17
卷期号:342 (6156): 361-363
被引量:134
标识
DOI:10.1126/science.1241460
摘要
Engineering radically altered genetic codes will allow for genomically recoded organisms that have expanded chemical capabilities and are isolated from nature. We have previously reassigned the translation function of the UAG stop codon; however, reassigning sense codons poses a greater challenge because such codons are more prevalent, and their usage regulates gene expression in ways that are difficult to predict. To assess the feasibility of radically altering the genetic code, we selected a panel of 42 highly expressed essential genes for modification. Across 80 Escherichia coli strains, we removed all instances of 13 rare codons from these genes and attempted to shuffle all remaining codons. Our results suggest that the genome-wide removal of 13 codons is feasible; however, several genome design constraints were apparent, underscoring the importance of a strategy that rapidly prototypes and tests many designs in small pieces.
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