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哺乳动物线粒体起始因子 3 存在下的翻译忠实性。

Fidelity of translation in the presence of mammalian mitochondrial initiation factor 3.

机构信息

Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore 560012, India.

Department of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3290, USA.

出版信息

Mitochondrion. 2018 Mar;39:1-8. doi: 10.1016/j.mito.2017.08.006. Epub 2017 Aug 10.

Abstract

Initiation factor 3 (IF3) is a conserved translation factor. Mutations in mitochondrial IF3 (IF3) have been implicated in disease pathology. Escherichia coli infCΔ55, compromised for IF3 activity, has provided an excellent heterologous system for IF3 structure-function analysis. IF3 allowed promiscuous initiation from AUA, AUU and ACG codons but avoided initiation with initiator tRNAs lacking the conserved 3GC pairs in their anticodon stems. Expression of IF3 N-terminal domain, or IF3 devoid of its typical N-, and C-terminal extensions improved fidelity of initiation in E. coli. The observations suggest that the IF3 terminal extensions relax the fidelity of translational initiation in mitochondria.

摘要

起始因子 3(IF3)是一种保守的翻译因子。线粒体 IF3(IF3)的突变与疾病发病机制有关。大肠杆菌 infCΔ55 缺乏 IF3 活性,为 IF3 结构功能分析提供了一个极好的异源系统。IF3 允许从 AUA、AUU 和 ACG 密码子随机起始,但避免与缺乏其反密码子茎中保守的 3GC 对的起始 tRNA 起始。IF3 N 端结构域的表达,或缺乏其典型的 N-和 C-端延伸的 IF3,提高了大肠杆菌起始的保真度。这些观察结果表明,IF3 末端延伸放松了线粒体翻译起始的保真度。

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