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RNA小螺旋的氨酰化:对氨酰tRNA合成酶结构设计和进化的启示

Aminoacylation of RNA minihelices: implications for tRNA synthetase structural design and evolution.

作者信息

Buechter D D, Schimmel P

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.

出版信息

Crit Rev Biochem Mol Biol. 1993;28(4):309-22. doi: 10.3109/10409239309078438.

Abstract

The genetic code is based on the aminoacylation of tRNA with amino acids catalyzed by the aminoacyl-tRNA synthetases. The synthetases are constructed from discrete domains and all synthetases possess a core catalytic domain that catalyzes amino acid activation, binds the acceptor stem of tRNA, and transfers the amino acid to tRNA. Fused to the core domain are additional domains that mediate RNA interactions distal to the acceptor stem. Several synthetases catalyze the aminoacylation of RNA oligonucleotide substrates that recreate only the tRNA acceptor stems. In one case, a relatively small catalytic domain catalyzes the aminoacylation of these substrates independent of the rest of the protein. Thus, the active site domain may represent a primordial synthetase in which polypeptide insertions that mediate RNA acceptor stem interactions are tightly integrated with determinants for aminoacyl adenylate synthesis. The relationship between nucleotide sequences in small RNA oligonucleotides and the specific amino acids that are attached to these oligonucleotides could constitute a second genetic code.

摘要

遗传密码基于氨酰 - tRNA合成酶催化的tRNA与氨基酸的氨酰化反应。合成酶由离散结构域构成,所有合成酶都拥有一个核心催化结构域,该结构域催化氨基酸活化、结合tRNA的受体茎,并将氨基酸转移至tRNA。与核心结构域融合的是其他结构域,这些结构域介导受体茎远端的RNA相互作用。几种合成酶催化仅重现tRNA受体茎的RNA寡核苷酸底物的氨酰化反应。在一种情况下,一个相对较小的催化结构域独立于蛋白质的其余部分催化这些底物的氨酰化反应。因此,活性位点结构域可能代表一种原始合成酶,其中介导RNA受体茎相互作用的多肽插入与氨酰腺苷酸合成的决定因素紧密整合。小RNA寡核苷酸中的核苷酸序列与连接到这些寡核苷酸上的特定氨基酸之间的关系可能构成第二种遗传密码。

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