Suppr超能文献

编码σE的基因在枯草芽孢杆菌中从一个类似σA的启动子转录而来。

Gene encoding sigma E is transcribed from a sigma A-like promoter in Bacillus subtilis.

作者信息

Kenney T J, Kirchman P A, Moran C P

机构信息

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

出版信息

J Bacteriol. 1988 Jul;170(7):3058-64. doi: 10.1128/jb.170.7.3058-3064.1988.

Abstract

Bacillus subtilis produces several RNA polymerase sigma factors. At least two of these factors are essential for endospore formation, sigma H, which is present in vegetative cells, and sigma E, which is produced exclusively after the start of endospore formation. The structural gene that encodes sigma E is part of the spoIIG operon, which is transcribed after the onset of sporulation. We have determined the starting point of transcription and the nucleotide sequence of the spoIIG promoter. This promoter contains sequences that are similar to those found at the -10 and -35 regions of promoters that are used by E sigma A, the primary form of RNA polymerase in vegetative cells. The unusual feature of this promoter is that these putative sigma A contact sites are separated by 22 base pairs, rather than the typical 17 or 18 base pairs. Single-base substitutions in the -10-like sequence reduced utilization of the spoIIG promoter in vivo. Furthermore, E sigma A, but not E sigma H and other secondary forms of RNA polymerase, accurately initiated transcription from the spoIIG promoter in an in vitro assay; therefore, we suggest that E sigma A transcribes the spoIIG operon in vivo. A base substitution in the -35-like sequence caused constitutive transcription from the promoter in vegetative cells; therefore, regulation of this sporulation-specific transcription may involve a novel mechanism.

摘要

枯草芽孢杆菌可产生多种RNA聚合酶σ因子。其中至少有两种因子对芽孢形成至关重要,即存在于营养细胞中的σH和仅在芽孢形成开始后产生的σE。编码σE的结构基因是spoIIG操纵子的一部分,该操纵子在芽孢形成开始后转录。我们已确定spoIIG启动子的转录起始点和核苷酸序列。该启动子含有与营养细胞中RNA聚合酶的主要形式EσA所使用的启动子的-10和-35区域中发现的序列相似的序列。该启动子的不同寻常之处在于,这些假定的σA接触位点相隔22个碱基对,而不是典型的17或18个碱基对。-10样序列中的单碱基取代降低了spoIIG启动子在体内的利用率。此外,在体外试验中,EσA能准确地从spoIIG启动子起始转录,而EσH和其他RNA聚合酶的二级形式则不能;因此,我们认为EσA在体内转录spoIIG操纵子。-35样序列中的一个碱基取代导致营养细胞中该启动子的组成型转录;因此,这种芽孢形成特异性转录的调控可能涉及一种新机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9214/211249/8b35282f3d52/jbacter00185-0181-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验