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Pap 相位变异的调控。在体外,Lrp 足以建立 pap DNA 甲基化模式的关闭相位并抑制 pap 转录。

Regulation of Pap phase variation. Lrp is sufficient for the establishment of the phase off pap DNA methylation pattern and repression of pap transcription in vitro.

作者信息

Weyand N J, Low D A

机构信息

Department of Molecular Biology, University of California, Santa Barbara, California 93106, USA.

出版信息

J Biol Chem. 2000 Feb 4;275(5):3192-200. doi: 10.1074/jbc.275.5.3192.

Abstract

The pyelonephritis-associated pili (pap) operon in Escherichia coli is regulated by an epigenetic mechanism involving the formation of specific DNA methylation patterns characteristic of transcriptionally active (phase ON) and inactive (phase OFF) cells. The formation of pap DNA methylation patterns in vivo was previously shown to require the leucine-responsive regulatory protein (Lrp) and DNA adenine methylase (Dam). To monitor the binding of Lrp to pap DNA, an in vitro methylation protection assay was developed. Binding of Lrp to a Dam target site proximal to the papBA promoter (designated GATC(prox)) blocked methylation of this site and specifically repressed transcription. The DNA methylation pattern and transcription state are identical to those observed in vivo in phase OFF cells. To determine if binding of Lrp at GATC(prox) was necessary for repression of papBA transcription, we analyzed a pap mutation (pap-13) that reduced the affinity of Lrp for the GATC(prox) region. Binding of Lrp to pap-13 DNA was shifted to a promoter distal Dam target site (designated GATC(dist)). Lrp blocked methylation of GATC(dist) in the pap-13 mutant, but did not repress papBA transcription. Together, these results show that binding of Lrp to the GATC(prox) region is sufficient for the establishment of the phase OFF DNA methylation pattern and repression of papBA transcription.

摘要

大肠杆菌中与肾盂肾炎相关的菌毛(pap)操纵子受一种表观遗传机制调控,该机制涉及形成具有转录活性(开启状态)和无活性(关闭状态)细胞特征的特定DNA甲基化模式。先前研究表明,体内pap DNA甲基化模式的形成需要亮氨酸应答调节蛋白(Lrp)和DNA腺嘌呤甲基化酶(Dam)。为监测Lrp与pap DNA的结合情况,开发了一种体外甲基化保护试验。Lrp与papBA启动子近端的Dam靶位点(命名为GATC(prox))结合会阻止该位点的甲基化,并特异性抑制转录。DNA甲基化模式和转录状态与体内关闭状态细胞中观察到的相同。为确定Lrp在GATC(prox)处的结合对于抑制papBA转录是否必要,我们分析了一个降低Lrp对GATC(prox)区域亲和力的pap突变(pap-13)。Lrp与pap-13 DNA的结合转移到了启动子远端的Dam靶位点(命名为GATC(dist))。在pap-13突变体中,Lrp阻止了GATC(dist)的甲基化,但并未抑制papBA转录。这些结果共同表明,Lrp与GATC(prox)区域的结合足以建立关闭状态的DNA甲基化模式并抑制papBA转录。

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