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一个枯草芽孢杆菌芽孢形成操纵子的特征分析,该操纵子包含一个RNA聚合酶σ因子基因和一个假定的D-羧肽酶基因。

Characterization of a Bacillus subtilis sporulation operon that includes genes for an RNA polymerase sigma factor and for a putative DD-carboxypeptidase.

作者信息

Wu J J, Schuch R, Piggot P J

机构信息

Department of Microbiology and Immunology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140.

出版信息

J Bacteriol. 1992 Aug;174(15):4885-92. doi: 10.1128/jb.174.15.4885-4892.1992.

DOI:10.1128/jb.174.15.4885-4892.1992
PMID:1629150
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC206299/
Abstract

At early stages of sporulation, the spoIIA locus is transcribed as a tricistronic (1.7-kb) operon, coding for sigma F and for two proteins that modulate the activity of sigma F. The locus is transcribed as a longer (2.9-kb) transcript at the late stages of sporulation. We show here that the longer transcript contains an additional open reading frame whose product has extensive sequence homology with DD-carboxypeptidases; the corresponding gene is designated dacF. Cotranscription of a morphogene, such as dacF, with the gene for a sigma factor suggests a way to couple transcription regulation with morphogenesis. The predicted N-terminal sequence of the DacF protein and the inhibition of sporulation by a translational dacF-lacZ fusion both suggest that the protein has a signal peptide for transport into or across a membrane. Expression of a dacF-lacZ transcriptional fusion was in the forespore. The 5' end of the 2.9-kb transcript was determined by primer extension analysis. The region 5' to the end showed no homology to promoters recognized by known sigma factors but was homologous to the corresponding region of the forespore-specific 0.3-kb gene of Bacillus subtilis.

摘要

在芽孢形成的早期阶段,spoIIA基因座作为一个三顺反子(1.7kb)操纵子进行转录,编码σF以及两种调节σF活性的蛋白质。在芽孢形成的后期阶段,该基因座转录为一个更长的(2.9kb)转录本。我们在此表明,更长的转录本包含一个额外的开放阅读框,其产物与DD-羧肽酶具有广泛的序列同源性;相应的基因被命名为dacF。一个形态发生基因(如dacF)与一个σ因子基因的共转录提示了一种将转录调控与形态发生相偶联的方式。DacF蛋白预测的N端序列以及一个翻译型dacF-lacZ融合对芽孢形成的抑制作用均表明该蛋白具有一个用于转运进入或穿过膜的信号肽。一个dacF-lacZ转录融合的表达发生在前芽孢中。通过引物延伸分析确定了2.9kb转录本的5'端。该末端5'端区域与已知σ因子识别的启动子没有同源性,但与枯草芽孢杆菌前芽孢特异性0.3kb基因的相应区域同源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c55a/206299/f19640b9fe63/jbacter00081-0035-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c55a/206299/244b4e71727f/jbacter00081-0033-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c55a/206299/bef0c2f7042e/jbacter00081-0035-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c55a/206299/f19640b9fe63/jbacter00081-0035-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c55a/206299/244b4e71727f/jbacter00081-0033-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c55a/206299/bef0c2f7042e/jbacter00081-0035-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c55a/206299/f19640b9fe63/jbacter00081-0035-b.jpg

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