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[为什么尚未发现终止tRNA?因为它们隐藏在大核糖体RNA中]

[Why termination tRNAs have not been found? Because they are hidden in the large ribosomal RNA].

作者信息

Ivanov V I, Beniaminov A D, Mikheev A N, Miniat E E

出版信息

Mol Biol (Mosk). 2001 Jul-Aug;35(4):718-26.

Abstract

It is well known that protein synthesis in ribosomes on mRNA requires two kinds of tRNAs: initiation and elongation. The former initiates the process (formylmethionine tRNA in prokaryotes and special methionine tRNA in eukaryotes). The latter participates in the synthesis proper, recognizing the sense codons. The synthesis is assisted by special proteins: initiation, elongation, and termination factors. The termination factors are necessary to recognize stop codons (UAG, UGA, and UAA) and to release the complete protein chain from the elongation tRNA preceding a stop codon. No termination tRNA capable of recognizing stop codons by its anticodon is known. The termination factors are thought to do this. We discovered in the large ribosomal RNA two regions that, like tRNAs, contain the anticodon hairpin, but with triplets complementary to stop codons. By analogy, we called them termination tRNAs (Ter-tRNA1 and Ter-tRNA2), though they transport no amino acids, and suggested them to directly recognize stop codons. The termination factors only condition such a recognition, making it specific and reliable (of course, they fulfill the hydrolysis of the ester bond between the polypeptide and tRNA). A strong argument in favor of our hypothesis came from vertebrate mitochondria. They acquired two new stop codons, AGA and AGG (in the standard code, they are two out of six arginine codons). We revealed that the corresponding anticodons appear in Ter-tRNA1.

摘要

众所周知,核糖体在信使核糖核酸(mRNA)上进行蛋白质合成需要两种转运核糖核酸(tRNA):起始tRNA和延伸tRNA。前者启动这一过程(原核生物中的甲酰甲硫氨酸tRNA和真核生物中的特殊甲硫氨酸tRNA)。后者参与实际的合成过程,识别有义密码子。合成过程由特殊蛋白质辅助:起始因子、延伸因子和终止因子。终止因子对于识别终止密码子(UAG、UGA和UAA)以及从终止密码子之前的延伸tRNA上释放完整的蛋白质链是必需的。目前还没有已知的能够通过其反密码子识别终止密码子的终止tRNA。人们认为终止因子能做到这一点。我们在大核糖体RNA中发现了两个区域,它们像tRNA一样,含有反密码子发夹结构,但带有与终止密码子互补的三联体。以此类推,我们称它们为终止tRNA(Ter-tRNA1和Ter-tRNA2),尽管它们不转运氨基酸,并建议它们直接识别终止密码子。终止因子只是促成这种识别,使其具有特异性和可靠性(当然,它们完成多肽与tRNA之间酯键的水解)。支持我们假设的一个有力证据来自脊椎动物线粒体。它们获得了两个新的终止密码子AGA和AGG(在标准密码子中,它们是六个精氨酸密码子中的两个)。我们发现相应的反密码子出现在Ter-tRNA1中。

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