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一种用于缩短RNA的蛋白质延伸:延长的延伸因子-Tu识别线虫线粒体中无T臂tRNA的D臂。

A protein extension to shorten RNA: elongated elongation factor-Tu recognizes the D-arm of T-armless tRNAs in nematode mitochondria.

作者信息

Sakurai Masayuki, Watanabe Yoh-ichi, Watanabe Kimitsuna, Ohtsuki Takashi

机构信息

Department of Integrated Biosciences, Graduate School of Frontier Sciences, University of Tokyo, Kashiwa, Chiba 277-8562, Japan.

出版信息

Biochem J. 2006 Oct 15;399(2):249-56. doi: 10.1042/BJ20060781.

Abstract

Nematode mitochondria possess extremely truncated tRNAs. Of 22 tRNAs, 20 lack the entire T-arm. The T-arm is necessary for the binding of canonical tRNAs and EF (elongation factor)-Tu (thermo-unstable). The nematode mitochondrial translation system employs two different EF-Tu factors named EF-Tu1 and EF-Tu2. Our previous study showed that nematode Caenorhabditis elegans EF-Tu1 binds specifically to T-armless tRNA. C. elegans EF-Tu1 has a 57-amino acid C-terminal extension that is absent from canonical EF-Tu, and the T-arm-binding residues of canonical EF-Tu are not conserved. In this study, the recognition mechanism of T-armless tRNA by EF-Tu1 was investigated. Both modification interference assays and primer extension analysis of cross-linked ternary complexes revealed that EF-Tu1 interacts not only with the tRNA acceptor stem but also with the D-arm. This is the first example of an EF-Tu recognizing the D-arm of a tRNA. The binding activity of EF-Tu1 was impaired by deletion of only 14 residues from the C-terminus, indicating that the C-terminus of EF-Tu1 is required for its binding to T-armless tRNA. These results suggest that C. elegans EF-Tu1 recognizes the D-arm instead of the T-arm by a mechanism involving its C-terminal region. This study sheds light on the co-evolution of RNA and RNA-binding proteins in nematode mitochondria.

摘要

线虫线粒体拥有极度截短的tRNA。在22种tRNA中,有20种缺少完整的T臂。T臂对于经典tRNA与EF(延伸因子)-Tu(热不稳定)的结合是必需的。线虫线粒体翻译系统采用两种不同的EF-Tu因子,分别名为EF-Tu1和EF-Tu2。我们之前的研究表明,线虫秀丽隐杆线虫的EF-Tu1特异性结合无T臂的tRNA。秀丽隐杆线虫的EF-Tu1具有一个57个氨基酸的C末端延伸,这在经典EF-Tu中不存在,并且经典EF-Tu的T臂结合残基并不保守。在本研究中,对EF-Tu1识别无T臂tRNA的机制进行了研究。交联三元复合物的修饰干扰试验和引物延伸分析均表明,EF-Tu1不仅与tRNA的受体茎相互作用,还与D臂相互作用。这是EF-Tu识别tRNA的D臂的首个实例。仅从C末端缺失14个残基就会损害EF-Tu1的结合活性,这表明EF-Tu1的C末端是其与无T臂tRNA结合所必需的。这些结果表明,秀丽隐杆线虫的EF-Tu1通过一种涉及其C末端区域的机制识别D臂而非T臂。本研究揭示了线虫线粒体中RNA与RNA结合蛋白的共同进化。

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