Suppr超能文献

一种RNA假结作为IncIα质粒ColIb-P9复制起始因子repZ基因翻译的分子开关。

An RNA pseudoknot as the molecular switch for translation of the repZ gene encoding the replication initiator of IncIalpha plasmid ColIb-P9.

作者信息

Asano K, Mizobuchi K

机构信息

Department of Biophysics and Biochemistry, Graduate School of Science, University of Tokyo, Hongo, Tokyo 113, Japan.

出版信息

J Biol Chem. 1998 May 8;273(19):11815-25. doi: 10.1074/jbc.273.19.11815.

Abstract

Translation initiation of the repZ gene encoding the replication initiator of plasmid ColIb-P9 is not only negatively regulated by the action of the antisense Inc RNA encoded in the leader region, but is also coupled to the translation and termination of a transcribed leader sequence, repY, a positive regulatory element for repZ gene expression. This translational coupling depends on base pairing between two complementary sequences, 5'-rGGCG-3' and 5'-rCGCC-3', which are located upstream of and in the middle of repY, respectively, and have the potential to form a pseudoknot with the stem-loop structure I. Another stem-loop called structure III near the 3'-end of repY sequesters both the 5'-rCGCC-3' sequence and the repZ ribosome-binding site. Here we show that the RepZ mRNA leader sequence synthesized in vitro indeed contains several stem-loop structures including structures I and III, but not the pseudoknot. However, disruption of structure III, without changing the repZ ribosome-binding site, by means of base substitution and deletion induces base pairing between the two short complementary sequences distantly separated, resulting in the formation of a pseudoknot. When the pseudoknot is allowed to form in vivo due to the same mutations, a maximum level of repZ expression is obtained comparable to one observed in the absence of Inc RNA. These results strengthen our previously proposed model that the pseudoknot induced by the translation and termination of the repY reading frame functions as the molecular switch for translational initiation of the repZ gene.

摘要

编码质粒ColIb - P9复制起始蛋白的repZ基因的翻译起始不仅受到前导区编码的反义Inc RNA作用的负调控,还与转录的前导序列repY的翻译和终止相偶联,repY是repZ基因表达的正调控元件。这种翻译偶联依赖于两个互补序列5'-rGGCG-3'和5'-rCGCC-3'之间的碱基配对,它们分别位于repY的上游和中间,并且有可能与茎环结构I形成假结。在repY的3'端附近的另一个茎环结构III隔离了5'-rCGCC-3'序列和repZ核糖体结合位点。在这里我们表明,体外合成的RepZ mRNA前导序列确实包含几个茎环结构,包括结构I和结构III,但不包含假结。然而,通过碱基替换和缺失破坏结构III而不改变repZ核糖体结合位点,会诱导远距离分离的两个短互补序列之间的碱基配对,从而导致假结的形成。当由于相同的突变在体内允许假结形成时,可获得与在没有Inc RNA时观察到的最高水平相当的repZ表达。这些结果强化了我们之前提出的模型,即repY阅读框的翻译和终止诱导的假结作为repZ基因翻译起始的分子开关。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验