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

机译:在稀有精氨酸密码子之后的终止密码子是大肠杆菌中SsrA标签的有效决定因素

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摘要

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.
机译:当核糖体停滞在mRNA上时,SsrA或tmRNA质量控制系统会介入,并指示添加靶向修饰多肽降解的C末端肽标签。尽管可以防止降解时在细胞中检测到数百种带有SsrA标签的蛋白质,但尚未鉴定出大多数此类物质。因此,导致核糖体停滞和SsrA标签的mRNA序列决定因素了解得很少。大肠杆菌核糖激酶的SsrA标签发生在该蛋白C末端处或附近的三个特定位点。标签的位点对应于核糖体在终止密码子和编码Arg-307和Arg-309的稀有AGG密码子(大肠杆菌核糖激酶的前倒数第二个和C末端残基)处失速。突变分析和对过表达AGG的tRNA过度表达的影响的研究表明,C末端稀有精氨酸密码子和相邻的无效UGA终止密码子的结合起招募SsrA标签系统的作用,大概是通过减慢翻译速度伸长和终止。

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