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枯草芽孢杆菌σD依赖型操纵子中鞭毛合成调控基因和结构基因的鉴定。

Identification of flagellar synthesis regulatory and structural genes in a sigma D-dependent operon of Bacillus subtilis.

作者信息

Mirel D B, Lauer P, Chamberlin M J

机构信息

Division of Biochemistry and Molecular Biology, University of California, Berkeley 94720.

出版信息

J Bacteriol. 1994 Aug;176(15):4492-500. doi: 10.1128/jb.176.15.4492-4500.1994.

Abstract

The sigma D form of RNA polymerase from Bacillus subtilis has been shown previously to direct the synthesis of several transcription units bearing genes for flagellin, motility proteins, and autolysins. In this report, we describe an operon of genes transcribed from the sigma D-dependent promoter PD-1. We have identified three complete open reading frames and one partial one downstream of this promoter; immediately upstream is the previously identified comF locus. The PD-1 operon encodes the presumptive B. subtilis homologs of two Salmonella typhimurium late flagellar genes, flgM and flgK. Also present in this operon are two genes of unknown function, orf139 and orf160, whose products show similarities to the eukaryotic cytoskeletal proteins myosin and vimentin, respectively. orf139 and orf160 may encode proteins that form extended alpha-helical secondary structures and coiled-coil quaternary structures which may be filamentous components of the gram-positive bacterial flagellum. We have characterized the B. subtilis flgM gene further by constructing an in-frame deletion mutation, flgM delta 80, and creating strains of B. subtilis in which this allele has replaced the wild-type copy. By primer extension analysis of cellular RNA, we have shown that the flgM delta 80 mutation relieves the block to transcription of two other sigma D-dependent operons imposed by an unlinked mutation in a gene directing early flagellar synthesis. We conclude that, as in the case of S. typhimurium, early flagellar synthesis in B. subtilis is coupled to late flagellar synthesis through repression of sigma D-dependent transcription by the flgM gene product.

摘要

先前已表明,来自枯草芽孢杆菌的RNA聚合酶的σD形式可指导合成多个转录单元,这些转录单元带有鞭毛蛋白、运动蛋白和自溶素的基因。在本报告中,我们描述了一个从依赖σD的启动子PD-1转录的基因操纵子。我们在该启动子下游鉴定出三个完整的开放阅读框和一个部分开放阅读框;紧挨着上游的是先前鉴定出的comF基因座。PD-1操纵子编码两种鼠伤寒沙门氏菌晚期鞭毛基因flgM和flgK在枯草芽孢杆菌中的推测同源物。该操纵子中还存在两个功能未知的基因orf139和orf160,它们的产物分别与真核细胞骨架蛋白肌球蛋白和波形蛋白相似。orf139和orf160可能编码形成延伸的α-螺旋二级结构和卷曲螺旋四级结构的蛋白质,这些结构可能是革兰氏阳性细菌鞭毛的丝状成分。我们通过构建框内缺失突变flgM delta 80并创建该等位基因已取代野生型拷贝的枯草芽孢杆菌菌株,进一步对枯草芽孢杆菌flgM基因进行了表征。通过对细胞RNA的引物延伸分析表明,flgM delta 80突变消除了由一个指导早期鞭毛合成的基因中的非连锁突变对另外两个依赖σD的操纵子转录的阻碍。我们得出结论,与鼠伤寒沙门氏菌的情况一样,枯草芽孢杆菌中的早期鞭毛合成通过flgM基因产物对依赖σD的转录的抑制与晚期鞭毛合成相偶联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/479c/196267/e87181b52706/jbacter00033-0041-a.jpg

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