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枯草芽孢杆菌gerK操纵子的转录,该操纵子编码一种芽孢萌发受体,并与编码其他萌发受体的操纵子进行比较。

Transcription of the Bacillus subtilis gerK operon, which encodes a spore germinant receptor, and comparison with that of operons encoding other germinant receptors.

作者信息

Igarashi Takao, Setlow Peter

机构信息

Department of Molecular, Microbial, and Structural Biology, University of Connecticut Health Center, Farmington, CT 06030-3305, USA.

出版信息

J Bacteriol. 2006 Jun;188(11):4131-6. doi: 10.1128/JB.00265-06.

Abstract

The gerA, gerB, and gerK operons, which encode germinant receptors in spores of Bacillus subtilis, were transcribed only in sporulation, and their mRNA levels peaked initially approximately 3 h before the initiation of accumulation of the spore's dipicolinic acid. After a rapid fall, levels of these mRNAs peaked again approximately 5 h later. In one wild-type strain (PS832), gerA mRNA was the most abundant, with levels of gerB and gerK mRNAs approximately 50% of that of gerA mRNA, whereas gerB mRNA was the most abundant in another wild-type strain (PY79). The synthesis of gerK mRNA in sporulation was abolished by loss of the forespore-specific RNA polymerase sigma factor, sigma(G), and induction of sigma(G) synthesis in vegetative cells led to synthesis of gerK mRNA. SpoVT, a regulator of sigma(G)-dependent gene expression, repressed gerK expression. The gerK promoter showed sequence similarities to sigma(G)-dependent promoters, and deletion of elements of this putative promoter abolished gerK expression in sporulation.

摘要

编码枯草芽孢杆菌孢子中萌发受体的gerA、gerB和gerK操纵子仅在孢子形成过程中被转录,且它们的mRNA水平最初在孢子中吡啶二羧酸积累开始前约3小时达到峰值。在快速下降后,这些mRNA水平约5小时后再次达到峰值。在一个野生型菌株(PS832)中,gerA mRNA最为丰富,gerB和gerK mRNA的水平约为gerA mRNA的50%,而在另一个野生型菌株(PY79)中gerB mRNA最为丰富。孢子形成过程中gerK mRNA的合成因前芽孢特异性RNA聚合酶σ因子σ(G)的缺失而被消除,在营养细胞中诱导σ(G)的合成导致gerK mRNA的合成。SpoVT是σ(G)依赖性基因表达的调节因子,可抑制gerK的表达。gerK启动子与σ(G)依赖性启动子具有序列相似性,该假定启动子元件的缺失消除了孢子形成过程中gerK的表达。

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