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参与大肠杆菌菌毛表达和相变的甲基化阻断因子(mbf)基因座的证据。

Evidence for a methylation-blocking factor (mbf) locus involved in pap pilus expression and phase variation in Escherichia coli.

作者信息

Braaten B A, Blyn L B, Skinner B S, Low D A

机构信息

Department of Pathology, University of Utah Medical Center, Salt Lake City 84132.

出版信息

J Bacteriol. 1991 Mar;173(5):1789-800. doi: 10.1128/jb.173.5.1789-1800.1991.

Abstract

Transcription of the pyelonephritis-associated pilus (pap) operon of Escherichia coli is subject to regulation by a phase variation control mechanism in which the pap pilin gene alternates between transcriptionally active (phase-on) and inactive (phase-off) states. Pap phase variation appears to involve differential inhibition of deoxyadenosine methylase (Dam) methylation of two pap GATC sites, GATC1028 and GATC1130, located in the regulatory region upstream of the papBA promoter. DNA from phase-on cells contains an unmethylated adenosine in the GATC1028 site, whereas DNA from phase-off cells contains an unmethylated adenosine in the GATC1130 site. papI and papB are two regulatory genes in the pap operon. Analysis of pap deletion mutants suggests that papI is required for methylation inhibition at the GATC1028 site; however, neither papI nor papB is required for inhibition of methylation at the GATC1130 site. We have identified a chromosomal locus, mbf (methylation-blocking factor), that is required for methylation protection of both the pap GATC1028 and GATC1130 sites. The mbf locus was identified after transposon mTn10 mutagenesis and mapped to 19.6 min on the E. coli chromosome. The effect of transposon mutations within mbf on pap pilin transcription was determined by using a papBAp-lac operon fusion which places lacZ under control of the papBA promoter. E. coli containing mbf::mTn10 and phase-off mbf+ E. coli cells both expressed beta-galactosidase levels about 30-fold lower than the beta-galactosidase level measured for phase-on mbf+ E. coli cells. These results indicated that mbf was necessary for pap pilin transcription and were supported by Northern (RNA) blotting and primer extension analyses. Moreover, transposon insertion within mbf greatly reduced Pap pilus expression. The mbf locus was isolated on a low-copy-number cosmid, pMBF1. Complementation analysis indicated that each of seven mbf::mTn10 mutants isolated contained a transposon insertion within the same gene or operon. The identification of the mbf locus, required for pap transcription, supports the hypothesis that pap phase variation is controlled by a mechanism involving alternation between different methylation states.

摘要

大肠杆菌肾盂肾炎相关菌毛(pap)操纵子的转录受一种相变控制机制的调节,在该机制中,pap菌毛蛋白基因在转录活性状态(开启相)和非活性状态(关闭相)之间交替。Pap相变似乎涉及对位于papBA启动子上游调控区域的两个pap GATC位点(GATC1028和GATC1130)的脱氧腺苷甲基化酶(Dam)甲基化的差异抑制。开启相细胞的DNA在GATC1028位点含有一个未甲基化的腺苷,而关闭相细胞的DNA在GATC1130位点含有一个未甲基化的腺苷。papI和papB是pap操纵子中的两个调控基因。对pap缺失突变体的分析表明,papI是GATC1028位点甲基化抑制所必需的;然而,GATC1130位点的甲基化抑制既不需要papI也不需要papB。我们鉴定出一个染色体位点mbf(甲基化阻断因子),它是pap GATC1028和GATC1130位点甲基化保护所必需的。mbf位点是在转座子mTn10诱变后鉴定出来的,并定位在大肠杆菌染色体的19.6分钟处。通过使用将lacZ置于papBA启动子控制下的papBAp - lac操纵子融合体,确定了mbf内转座子突变对pap菌毛蛋白转录的影响。含有mbf::mTn10的大肠杆菌和关闭相的mbf +大肠杆菌细胞表达的β - 半乳糖苷酶水平均比开启相的mbf +大肠杆菌细胞测得的β - 半乳糖苷酶水平低约30倍。这些结果表明mbf是pap菌毛蛋白转录所必需的,Northern(RNA)印迹和引物延伸分析也支持了这一点。此外,mbf内的转座子插入极大地降低了Pap菌毛的表达。mbf位点在一个低拷贝数粘粒pMBF1上分离出来。互补分析表明,分离出的七个mbf::mTn10突变体中的每一个都在同一基因或操纵子内含有一个转座子插入。对pap转录所必需的mbf位点的鉴定支持了这样一种假说,即pap相变是由一种涉及不同甲基化状态之间交替的机制控制的。

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