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放线菌中的T盒核糖开关:通过新型tRNA相互作用进行翻译调控

T box riboswitches in Actinobacteria: translational regulation via novel tRNA interactions.

作者信息

Sherwood Anna V, Grundy Frank J, Henkin Tina M

机构信息

Molecular, Cellular, and Developmental Biology Graduate Program, Center for RNA Biology, and.

Center for RNA Biology, and Department of Microbiology, The Ohio State University, Columbus, OH 43210.

出版信息

Proc Natl Acad Sci U S A. 2015 Jan 27;112(4):1113-8. doi: 10.1073/pnas.1424175112. Epub 2015 Jan 12.

Abstract

The T box riboswitch regulates many amino acid-related genes in Gram-positive bacteria. T box riboswitch-mediated gene regulation was shown previously to occur at the level of transcription attenuation via structural rearrangements in the 5' untranslated (leader) region of the mRNA in response to binding of a specific uncharged tRNA. In this study, a novel group of isoleucyl-tRNA synthetase gene (ileS) T box leader sequences found in organisms of the phylum Actinobacteria was investigated. The Stem I domains of these RNAs lack several highly conserved elements that are essential for interaction with the tRNA ligand in other T box RNAs. Many of these RNAs were predicted to regulate gene expression at the level of translation initiation through tRNA-dependent stabilization of a helix that sequesters a sequence complementary to the Shine-Dalgarno (SD) sequence, thus freeing the SD sequence for ribosome binding and translation initiation. We demonstrated specific binding to the cognate tRNA(Ile) and tRNA(Ile)-dependent structural rearrangements consistent with regulation at the level of translation initiation, providing the first biochemical demonstration, to our knowledge, of translational regulation in a T box riboswitch.

摘要

T盒核糖开关调控革兰氏阳性菌中许多与氨基酸相关的基因。先前研究表明,T盒核糖开关介导的基因调控发生在转录衰减水平,通过mRNA的5'非翻译(前导)区域的结构重排来响应特定空载tRNA的结合。在本研究中,对放线菌门生物中发现的一组新的异亮氨酰-tRNA合成酶基因(ileS)T盒前导序列进行了研究。这些RNA的茎I结构域缺乏一些高度保守的元件,而这些元件对于与其他T盒RNA中的tRNA配体相互作用至关重要。据预测,许多此类RNA通过依赖tRNA稳定一个螺旋来调控翻译起始水平的基因表达,该螺旋可隔离与Shine-Dalgarno(SD)序列互补的序列,从而使SD序列可用于核糖体结合和翻译起始。我们证明了与同源tRNA(Ile)的特异性结合以及依赖tRNA的结构重排,这与翻译起始水平的调控一致,据我们所知,这首次在生化层面证明了T盒核糖开关中的翻译调控。

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