Zhang J, Ichikawa H, Halberg R, Kroos L, Aronson A I
Department of Biological Sciences, Purdue University, West Lafayette, IN 47907.
J Mol Biol. 1994 Jul 29;240(5):405-15. doi: 10.1006/jmbi.1994.1456.
The pattern of transcription has been examined for a cluster of genes encoding polypeptides some or all of which are assembled into a cross-linked component of the Bacillus subtilis spore coat. Three promoters, designated PVWX, PX and PYZ, were indicated by reverse transcriptase mapping. On the basis of Northern hybridization, it appeared that the cotV, W and X genes were transcribed as a polycistronic mRNA from PVWX as well as a monocistronic cotX mRNA from Px. The cotY and cotZ genes are cotranscribed from the PYZ promoter with a smaller cotY mRNA resulting from premature termination or RNA processing. All four transcripts were synthesized late during sporulation and were not produced in mutants lacking sigma K, which directs RNA polymerase to transcribe genes in the mother-cell compartment of sporulating cells. The DNA-binding protein GerE, which affects transcription of many genes in the mother cell during the late stages of sporulation, was also shown to be involved. There was essentially no cotX mRNA in a gerE mutant and the amounts of cotVWX, cotYZ and cotY mRNAs were somewhat reduced. In vitro run-off transcription studies with sigma K RNA polymerase and GerE confirmed the presence of the three promoters, and directly showed that GerE was necessary for transcription from PX as well as enhanced transcription from the PVWX and PYZ promoters. The DNase I footprints of GerE for all three promoters were immediately upstream of the -35 regions. These GerE binding sites were compared to those in other GerE-responsive promoters and a larger consensus sequence for GerE binding was recognized. This complex transcriptional pattern of the cotVWXYZ cluster is probably necessary to ensure that an optimal amount of each protein is made for the assembly of the spore coat.
已经对一组编码多肽的基因的转录模式进行了研究,其中部分或全部多肽组装成枯草芽孢杆菌芽孢衣的交联成分。通过逆转录酶定位确定了三个启动子,分别命名为PVWX、PX和PYZ。根据Northern杂交结果,cotV、W和X基因似乎从PVWX转录为多顺反子mRNA,同时也从Px转录为单顺反子cotX mRNA。cotY和cotZ基因从PYZ启动子共转录,由于过早终止或RNA加工产生较小的cotY mRNA。所有这四种转录本在芽孢形成后期合成,在缺乏σK的突变体中不产生,σK可引导RNA聚合酶转录芽孢形成细胞母细胞区室中的基因。还表明,在芽孢形成后期影响母细胞中许多基因转录的DNA结合蛋白GerE也参与其中。在gerE突变体中基本上没有cotX mRNA,cotVWX、cotYZ和cotY mRNA的量有所减少。用σK RNA聚合酶和GerE进行的体外径流转录研究证实了这三个启动子的存在,并直接表明GerE对于从PX转录是必需的,同时增强了从PVWX和PYZ启动子的转录。GerE对所有三个启动子的DNase I足迹位于-35区的紧邻上游。将这些GerE结合位点与其他GerE反应性启动子中的位点进行比较,识别出了更大的GerE结合共有序列。cotVWXYZ基因簇这种复杂的转录模式可能是确保为芽孢衣组装产生最佳量的每种蛋白质所必需的。