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Transcription analysis of the dnaA gene and oriC region of the chromosome of Mycobacterium smegmatis and Mycobacterium bovis BCG, and its regulation by the DnaA protein

机译:分枝杆菌染色体和肉杆菌BOVG染色体的DNAA基因和ORIC区的转录分析及其对DNAA蛋白的调控

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摘要

The regions flanking the Mycobacterium dnaA gene have extensive sequence conservation, and comprise various DnaA boxes. Comparative analysis of the dnaA promoter and oriC region from several mycobacterial species revealed that the localization, spacing and orientation of the DnaA boxes are conserved. Detailed transcriptional analysis in M. smegmatis and M. bovis BCG shows that the dnaN gene of both species and the dnaA gene of M. bovis BCG are transcribed from two promoters, whereas the dnaA gene of M. smegmatis is transcribed from a single promoter. RT-PCR with total RNA showed that dnaA and dnaN were expressed in both species at all growth stages. Analysis of the promoter activity using dnaA–gfp fusion plasmids and DnaA expression plasmids indicates that the dnaA gene is autoregulated, although the degree of transcriptional autorepression was moderate. Transcription was also detected in the vicinity of oriC of M. bovis BCG, but not of M. smegmatis. These results suggest that a more complex transcriptional mechanism may be involved in the slow-growing mycobacteria, which regulates the expression of dnaA and initiation of chromosomal DNA replication.
机译:侧翼所述分枝杆菌基因的地区具有广泛的序列保护,并包含各种DNAA箱。来自几种分枝杆菌物种的DNAA启动子和口腔区域的比较分析显示,DNAA箱的定位,间隔和取向是保守的。 M. Smogmatis和M.Bovis BCG的详细转录分析表明,来自两个启动子的肉豆肉BCG的DNAA基因的DNAN基因与两个启动子转录,而M. Smogmatis的DNAA基因由单一启动子转录。具有总RNA的RT-PCR显示DNAA和DNAN在所有生长阶段的两种物种中表达。使用DNAA-GFP融合质粒和DNAA表达质粒的启动子活性分析表明,虽然转录自动压缩程度为中等,但是自动调节DNAA基因。在M.Bovis Bcg的oric的oric附近也检测到转录,但不是M. Smogmatis。这些结果表明,更复杂的转录机制可能涉及缓慢生长的分枝杆菌,其调节DNAA的表达和染色体DNA复制的开始。

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