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转运RNA的结构与编码特异性。I. D臂突变降低tRNA从核糖体解离的证据。

Transfer RNA structure and coding specificity. I. Evidence that a D-arm mutation reduces tRNA dissociation from the ribosome.

作者信息

Smith D, Yarus M

机构信息

Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder 80309.

出版信息

J Mol Biol. 1989 Apr 5;206(3):489-501. doi: 10.1016/0022-2836(89)90496-8.

Abstract

The mutation G to A24 in the D-arm of Escherichia coli tRNA(Trp) or its UAG suppressor derivative Su7 has two known phenotypes: (1) an altered or relaxed coding specificity at the codon third position; and (2) partial rescue of an anticodon loop mutation. In order to study the mechanism responsible for these effects we constructed, by in vitro mutagenesis, a series of tRNAs with alterations in the anticodon loop or at the third position of the anticodon. Evaluation of the effects of the A24 mutation on the in vivo ribosomal activity of these tRNAs leads us to conclude that the mutation reduces the rate at which the ribosome is able to reject tRNAs that are structurally defective or non-cognate. The apparent interaction of the D-arm mutation with the anticodon and anticodon loop is thus primarily kinetic, rather than through the structure of the tRNA. The Appendix describes the calculation of tRNA ribosomal activity from in vivo measurement of suppression efficiency.

摘要

大肠杆菌tRNA(Trp) D臂中从G到A24的突变或其UAG抑制衍生物Su7有两种已知表型:(1) 密码子第三位的编码特异性改变或松弛;(2) 反密码子环突变的部分挽救。为了研究造成这些效应的机制,我们通过体外诱变构建了一系列反密码子环或反密码子第三位有改变的tRNA。评估A24突变对这些tRNA体内核糖体活性的影响后,我们得出结论,该突变降低了核糖体拒绝结构有缺陷或非同源tRNA的速率。因此,D臂突变与反密码子及反密码子环之间明显的相互作用主要是动力学上的,而非通过tRNA的结构。附录描述了根据体内抑制效率测量计算tRNA核糖体活性的方法。

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