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在大肠杆菌中,由稀有精氨酸密码子引导的终止密码子是SsrA标签的有效决定因素。

Stop codons preceded by rare arginine codons are efficient determinants of SsrA tagging in Escherichia coli.

作者信息

Hayes Christopher S, Bose Baundauna, Sauer Robert T

机构信息

Department of Biology, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.

出版信息

Proc Natl Acad Sci U S A. 2002 Mar 19;99(6):3440-5. doi: 10.1073/pnas.052707199. Epub 2002 Mar 12.

Abstract

The SsrA or tmRNA quality control system intervenes when ribosomes stall on mRNAs and directs the addition of a C-terminal peptide tag that targets the modified polypeptide for degradation. Although hundreds of SsrA-tagged proteins can be detected in cells when degradation is prevented, most of these species have not been identified. Consequently, the mRNA sequence determinants that cause ribosome stalling and SsrA tagging are poorly understood. SsrA tagging of Escherichia coli ribokinase occurs at three specific sites at or near the C terminus of this protein. The sites of tagging correspond to ribosome stalling at the termination codon and at rare AGG codons encoding Arg-307 and Arg-309, the antepenultimate and C-terminal residues of E. coli ribokinase. Mutational analyses and studies of the effects of overexpressing the tRNA that decodes AGG reveal that the combination of a rare arginine codon at the C terminus and the adjacent inefficient UGA termination codon act to recruit the SsrA-tagging system, presumably by slowing the rate of translation elongation and termination.

摘要

当核糖体在信使核糖核酸(mRNA)上停滞时,SsrA(或转运信使核糖核酸,tmRNA)质量控制系统会介入,并指导添加一个C末端肽标签,该标签会将修饰后的多肽靶向降解。尽管在防止降解时可以在细胞中检测到数百种带有SsrA标签的蛋白质,但其中大多数种类尚未被鉴定出来。因此,导致核糖体停滞和SsrA标签化的mRNA序列决定因素仍知之甚少。大肠杆菌核糖激酶的SsrA标签化发生在该蛋白质C末端或其附近的三个特定位点。标签化位点对应于核糖体在终止密码子以及编码大肠杆菌核糖激酶倒数第二个和C末端残基精氨酸-307和精氨酸-309的罕见AGG密码子处的停滞。对解码AGG的转运核糖核酸(tRNA)进行过表达的突变分析和研究表明,C末端的罕见精氨酸密码子与相邻的低效UGA终止密码子的组合作用是招募SsrA标签系统,大概是通过减缓翻译延伸和终止的速率来实现的。

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