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转运RNA中的反密码子移位:错义抑制和无义抑制的一种新机制。

Anticodon shift in tRNA: a novel mechanism in missense and nonsense suppression.

作者信息

Murgola E J, Prather N E, Mims B H, Pagel F T, Hijazi K A

出版信息

Proc Natl Acad Sci U S A. 1983 Aug;80(16):4936-9. doi: 10.1073/pnas.80.16.4936.

Abstract

In a previous publication, an unusual UGG-reading missense suppressor caused by insertion of an extra adenylate residue in the anticodon loop of an Escherichia coli glycine tRNA was described. In this study, we provide in vivo evidence that the additional nucleotide causes an "anticodon shift" by one nucleotide in the 3' direction and that the "new" anticodon can explain the unanticipated coding properties of the suppressor. We converted the UGG suppressor with ethyl methanesulfonate, a base-substitution mutagen, to suppressors that read codons related to UGG by a single base change. Sequence analysis of each mutant tRNA revealed that its mutational alteration was an anticipated base change in one of the three nucleotides of the "new" anticodon. Although the new suppressors read codons beginning with A or U, the mutant tRNAs lack the customary hypermodified nucleosides on the 3' side of the anticodon. As determined on the basis of their in vivo coding specificities, the new mutant tRNAs do not continue to utilize the original anticodon triplet for decoding. Furthermore, the failure of the UGG suppressor to correct frameshift mutations throughout each of three genes of the trp operon suggests that the addition of a nucleotide to the anticodon loop of a tRNA does not necessarily result in out-of-frame decoding by the tRNA. Therefore, a "frameshift" mutation in a tRNA has principally changed the triplet codon recognition properties of the molecule.

摘要

在之前的一篇出版物中,描述了一种不寻常的UGG阅读错义抑制子,它是由在大肠杆菌甘氨酸tRNA的反密码子环中插入一个额外的腺苷酸残基引起的。在本研究中,我们提供了体内证据,表明额外的核苷酸会导致反密码子在3'方向上发生一个核苷酸的“反密码子移位”,并且“新的”反密码子可以解释该抑制子意外的编码特性。我们用甲磺酸乙酯(一种碱基置换诱变剂)将UGG抑制子转化为通过单个碱基变化读取与UGG相关密码子的抑制子。对每个突变tRNA的序列分析表明,其突变改变是“新的”反密码子三个核苷酸之一的预期碱基变化。尽管新的抑制子读取以A或U开头的密码子,但突变tRNA在反密码子的3'侧缺乏通常的超修饰核苷。根据它们在体内的编码特异性确定,新的突变tRNA不再利用原来的反密码子三联体进行解码。此外,UGG抑制子未能校正色氨酸操纵子三个基因中每个基因的移码突变,这表明在tRNA的反密码子环中添加一个核苷酸不一定会导致tRNA进行移码解码。因此,tRNA中的“移码”突变主要改变了该分子的三联体密码子识别特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9262/384162/3493e4771dff/pnas00642-0069-a.jpg

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