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spo0E基因产物对枯草芽孢杆菌芽孢形成的负调控

Negative regulation of Bacillus subtilis sporulation by the spo0E gene product.

作者信息

Perego M, Hoch J A

机构信息

Department of Molecular and Experimental Medicine, Research Institute of Scripps Clinic, La Jolla, California 92037.

出版信息

J Bacteriol. 1991 Apr;173(8):2514-20. doi: 10.1128/jb.173.8.2514-2520.1991.

DOI:10.1128/jb.173.8.2514-2520.1991
PMID:1901567
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC207815/
Abstract

Transcription of the Bacillus subtilis spo0E gene is controlled by the AbrB transition state regulator. In AbrB+ strains, a single transcript, P1, was observed for the spo0E gene. In an abrB4 mutant strain, a second transcription start site 3 bases upstream from P1 was found to be used for the predominant transcript. P1 transcription was insensitive to the state of the abrB gene. Mutants carrying deletion or antibiotic cassette insertion mutations in the spo0E gene were Spo+. Multiple copies of the spo0E gene, not just the promoter region, were found to render strains incapable of sporulation. Spo+ strains that arose spontaneously from such Spo- strains were found to have deletions in the spo0E coding sequence on the plasmid. Strains carrying a deletion of the spo0E gene segregated Spo- colonies. These colonies were found to have secondary mutations in or near the spo0A, spo0B, or spo0F gene, suggesting that deletion of the spo0E gene results in increased pressure to sporulate that is compensated for by inactivation of one or more of the components of the signal transduction system leading to the initiation of sporulation. spo0E deletions were suppressors of the spo0F221 missense mutation but had no effect on the regulation of the spo0F, kinA, spo0A, or spo0B genes. The results suggest that the spo0E gene product is a negative regulator of the signal transduction pathway leading to sporulation.

摘要

枯草芽孢杆菌spo0E基因的转录受AbrB过渡态调节因子的控制。在AbrB+菌株中,spo0E基因观察到一个单一转录本P1。在abrB4突变菌株中,发现P1上游3个碱基处的第二个转录起始位点被用于主要转录本。P1转录对abrB基因的状态不敏感。在spo0E基因中携带缺失或抗生素盒插入突变的突变体是Spo+。发现spo0E基因的多个拷贝(不仅仅是启动子区域)会使菌株无法形成芽孢。从这些Spo-菌株中自发产生的Spo+菌株在质粒上的spo0E编码序列中存在缺失。携带spo0E基因缺失的菌株分离出Spo-菌落。发现这些菌落在spo0A、spo0B或spo0F基因中或其附近有二次突变,这表明spo0E基因的缺失导致形成芽孢的压力增加,这通过导致芽孢形成起始的信号转导系统的一个或多个组分的失活来补偿。spo0E缺失是spo0F221错义突变的抑制子,但对spo0F、kinA、spo0A或spo0B基因的调控没有影响。结果表明spo0E基因产物是导致芽孢形成的信号转导途径的负调节因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/820e/207815/5be7f330846b/jbacter00098-0114-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/820e/207815/5be7f330846b/jbacter00098-0114-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/820e/207815/5be7f330846b/jbacter00098-0114-a.jpg

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