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小肠结肠炎耶尔森菌III型分泌系统:yscM1和yscM2通过一种靶向yop mRNA 5'非翻译区的转录后机制调节yop基因表达。

Yersinia enterocolitica type III secretion: yscM1 and yscM2 regulate yop gene expression by a posttranscriptional mechanism that targets the 5' untranslated region of yop mRNA.

作者信息

Cambronne Eric D, Schneewind Olaf

机构信息

Committee on Microbiology, University of Chicago, 920 East 85th Street, Chicago, IL 60637, USA.

出版信息

J Bacteriol. 2002 Nov;184(21):5880-93. doi: 10.1128/JB.184.21.5880-5893.2002.

Abstract

Pathogenic Yersinia spp. secrete Yops (Yersinia outer proteins) via the type III pathway. The expression of yop genes is regulated in response to environmental cues, which results in a cascade of type III secretion reactions. yscM1 and yscM2 negatively regulate the expression of Yersinia enterocolitica yop genes. It is demonstrated that yopD and lcrH are required for yscM1 and yscM2 function and that all four genes act synergistically at the same regulatory step. Further, SycH binding to the protein products of yscM1 and yscM2 can activate yop gene expression even without promoting type III transport of YscM1 and YscM2. Reverse transcription-PCR analysis of yopQ mRNA as well as yopQ and yopE gene fusion experiments with the npt (neomycin phosphotransferase) reporter suggest that yscM1 and yscM2 regulate expression at a posttranscriptional step. The 178-nucleotide 5' untranslated region (UTR) of yopQ mRNA was sufficient to confer yscM1 and yscM2-mediated regulation on the fused reporter, as was the 28-nucleotide UTR of yopE. The sequence 5'-AUAAA-3' is located in the 5' yop UTRs, and mutations that alter the sequence motif either reduced or abolished yscM1- and yscM2-mediated regulation. A model is proposed whereby YopD, LcrH, YscM1, YscM2, and SycH regulate yop expression in response to specific environmental cues and by a mechanism that may involve binding of some of these factors to a specific target sequence within the UTR of yop mRNAs.

摘要

致病性耶尔森氏菌属通过III型分泌途径分泌Yops(耶尔森氏菌外膜蛋白)。yop基因的表达受环境信号调节,从而引发一系列III型分泌反应。yscM1和yscM2对小肠结肠炎耶尔森氏菌yop基因的表达起负调控作用。研究表明,yopD和lcrH是yscM1和yscM2发挥功能所必需的,且这四个基因在同一调控步骤协同作用。此外,SycH与yscM1和yscM2的蛋白质产物结合,即使不促进YscM1和YscM2的III型转运,也能激活yop基因表达。对yopQ mRNA的逆转录聚合酶链反应分析以及使用npt(新霉素磷酸转移酶)报告基因进行的yopQ和yopE基因融合实验表明,yscM1和yscM2在转录后水平调节表达。yopQ mRNA的178个核苷酸的5'非翻译区(UTR)足以赋予yscM1和yscM2对融合报告基因的调控作用,yopE的28个核苷酸的UTR也是如此。序列5'-AUAAA-3'位于yop的5'UTR中,改变该序列基序的突变会降低或消除yscM1和yscM2介导的调控。据此提出一个模型,即YopD、LcrH、YscM1、YscM2和SycH根据特定环境信号,通过一种可能涉及这些因子中某些与yop mRNA的UTR内特定靶序列结合的机制来调节yop表达。

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