Differential expression of 10 sigma factor genes in Mycobacterium tuberculosis

• Published in: Molecular microbiology 1999-01, Vol.31 (2), p.715-724
• Main Authors: Manganelli, Riccardo, Dubnau, Eugenie, Tyagi, Sanjay, Kramer, Fred Russell, Smith, Issar
• Format: Article
• Language: English
• Subjects: Bacterial Proteins - genetics; Culture Media; DNA-Directed RNA Polymerases - genetics; Gene Expression Regulation, Bacterial; Mycobacterium tuberculosis; Mycobacterium tuberculosis - genetics; Mycobacterium tuberculosis - growth & development; Reverse Transcriptase Polymerase Chain Reaction - methods; RNA, Messenger; Sigma Factor - genetics; Time Factors
• ISSN: 0950-382X; 1365-2958
• DOI: 10.1046/j.1365-2958.1999.01212.x

The ability of Mycobacterium tuberculosis to adapt to different environments in the infected host is essential for its pathogenicity. Consequently, this organism must be able to modulate gene expression to respond to the changing conditions it encounters during infection. In this paper we begin a comprehensive study of M. tuberculosis gene regulation, characterizing the transcript levels of 10 of its 13 putative sigma factor genes. We developed a real‐time RT‐PCR assay using a family of novel fluorescent probes called molecular beacons to quantitatively measure the different mRNAs. Three sigma factor genes were identified that have increased mRNA levels after heat shock, two of which also responded to detergent stress. In addition, we also identified a sigma factor gene whose mRNA increased after mild cold shock and a second that responded to conditions of low aeration.