作者: Heui-Dong Park , Kristi M. Guinn , Maria I. Harrell , Reiling Liao , Martin I. Voskuil
DOI: 10.1046/J.1365-2958.2003.03474.X
关键词: Regulatory sequence 、 Biology 、 Regulation of gene expression 、 Response regulator 、 Gene 、 Gene targeting 、 Cell biology 、 Genetics 、 Mutant 、 Mycobacterium tuberculosis 、 Transcription factor
摘要: Unlike many pathogens that are overtly harmful to their hosts, Mycobacterium tuberculosis can persist for years within humans in a clinically latent state. Latency is often linked hypoxic conditions the host. Among M. genes induced by hypoxia putative transcription factor, Rv3133c/DosR. We performed targeted disruption of this locus followed transcriptome analysis wild-type and mutant bacilli. Nearly all powerfully regulated require Rv3133c/DosR induction. Computer identified consensus motif, variant which located upstream nearly rapidly hypoxia. Further, binds two copies motif response gene alpha-crystallin. Mutations binding sites abolish both as well induction downstream reporter gene. Also, mutation experiments with confirmed sequence-based predictions C-terminus responsible DNA aspartate at position 54 essential function. Together, these results demonstrate factor two-component regulator class, it primary mediator signal tuberculosis.