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首页> 外文期刊>Nucleic acids research >Nonsense suppressor and antisuppressor mutations at the 1409–1491 base pair in the decoding region of Escherichia coli 16S rRNA Steven
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Nonsense suppressor and antisuppressor mutations at the 1409–1491 base pair in the decoding region of Escherichia coli 16S rRNA Steven

机译:Escherichia coli 16S rRNA Steven区域中1409–1491碱基对的无意义抑制子和抗抑制子突变

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Using a genetic selection for suppressors of a UGA nonsense mutation in trpA, we have isolated a G to A transition mutation at position 1491 in the decoding region of 6S rRNA. This suppressor displayed no codon specificity, suppressing UGA, UAG and UAA nonsense mutations and +1 and ?1 frameshlft mutations in lacZ. ubsequent examination of a series of mutations at G1491 and its base-pairing partner 409 revealed various effects on nonsense suppression and frameshrfting. Mutations that prevented Watson-Crick base pairing between these residues were observed to increase misreading and frameshiftlng. However, double mutations that retained pairing potential produced an antisuppressor or hyperaccurate phenotype. Previous studies of antibiotic resistance mutations and antibiotic and tRNA footprints have placed G1491 and C1409 near the site of codon-anticodon pairing. The results of this study demonstrate that the nature of the interaction of these two residues influences the fidelity of tRNA selection.
机译:使用遗传选择trpA中的UGA无意义突变的抑制子,我们在6S rRNA解码区域的1491位分离出了从G到A的转变突变。该抑制剂没有密码子特异性,可抑制lacZ中的UGA,UAG和UAA无意义突变以及+1和?1 framehlft突变。对G1491及其碱基配对伴侣409处的一系列突变的后续检查揭示了对废话抑制和构图缩短的各种影响。观察到阻止这些残基之间的沃森-克里克碱基配对的突变会增加误读和移码。但是,保留配对潜力的双突变产生了抗抑制剂或超准确的表型。先前对抗生素抗性突变以及抗生素和tRNA足迹的研究已将G1491和C1409置于密码子与反密码子配对位点附近。这项研究的结果表明,这两个残基相互作用的性质影响tRNA选择的保真度。

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