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枯草芽孢杆菌中一个对依赖Spo0A的启动子活性必需的σH区域。

A region in Bacillus subtilis sigmaH required for Spo0A-dependent promoter activity.

作者信息

Buckner C M, Moran C P

机构信息

Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

出版信息

J Bacteriol. 1998 Sep;180(18):4987-90. doi: 10.1128/JB.180.18.4987-4990.1998.

Abstract

Spo0A activates transcription in Bacillus subtilis from promoters that are used by two types of RNA polymerase, RNA polymerase containing the primary sigma factor, sigmaA, and RNA polymerase containing a secondary sigma factor, known as sigmaH. The region of sigmaA near positions 356 to 359 is required for Spo0A-dependent promoter activation, possibly because Spo0A interacts with this region of sigmaA at these promoters. To determine if the amino acids in the corresponding region of sigmaH are also important in Spo0A-dependent promoter activation, we examined the effects of single alanine substitutions at 10 positions in sigmaH (201 to 210). Two alanine substitutions in sigmaH, at glutamine 201 (Q201A) and at arginine 205 (R205A), significantly decreased activity from the Spo0A-dependent, sigmaH-dependent promoter spoIIA but did not affect expression from the sigmaH-dependent, Spo0A-independent promoters citGp2 and spoVG. Therefore, promoter activation by Spo0A requires homologous regions in sigmaA and sigmaH. A mutant form of Spo0A, S231F, that suppresses the sporulation defect caused by several amino acid substitutions in sigmaA did not suppress the sporulation defects caused by the Q201A and R205A substitutions in sigmaH. This result and others indicate that different surfaces of Spo0A probably interact with sigmaA and sigmaH RNA polymerases.

摘要

Spo0A在枯草芽孢杆菌中可激活两种RNA聚合酶所使用的启动子的转录,这两种RNA聚合酶分别是含有主要σ因子σA的RNA聚合酶和含有次要σ因子(称为σH)的RNA聚合酶。σA靠近356至359位的区域是Spo0A依赖性启动子激活所必需的,这可能是因为Spo0A在这些启动子处与σA的该区域相互作用。为了确定σH相应区域中的氨基酸在Spo0A依赖性启动子激活中是否也很重要,我们研究了σH中10个位置(201至210)的单个丙氨酸取代的影响。σH中的两个丙氨酸取代,即谷氨酰胺201(Q201A)和精氨酸205(R205A),显著降低了Spo0A依赖性、σH依赖性启动子spoIIA的活性,但不影响σH依赖性、Spo0A非依赖性启动子citGp2和spoVG的表达。因此,Spo0A对启动子的激活需要σA和σH中的同源区域。一种抑制由σA中几个氨基酸取代引起的孢子形成缺陷的Spo0A突变形式S231F,不能抑制由σH中的Q201A和R205A取代引起的孢子形成缺陷。这一结果及其他结果表明,Spo0A的不同表面可能与σA和σH RNA聚合酶相互作用。

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