Structural highlights
FunctionPublication Abstract from PubMedMycobacterium tuberculosis thrives in oxidative environments such as the macrophage. In order to survive the bacterium must sense and adapt to the oxidative conditions. Several antioxidant defenses including a thick cell wall, millimolar concentrations of small molecule thiols and protective enzymes are known to help the bacterium withstand the oxidative stress. However, oxidation-sensing regulators that control these defenses have remained elusive. In this paper, we report a new oxidation-sensing regulator, Rv1049 or MosR (Mycobacterium tuberculosis oxidation-sensing Regulator). MosR is a transcriptional repressor of the MarR family, which, similarly to B. subtilis OhrR and S. aureus MgrA, dissociates from DNA in the presence of oxidants, enabling transcription. MosR senses oxidation through a pair of cysteines near the N-terminus (Cys10 and Cys12) that upon oxidation forms a disulfide bond. Disulfide formation rearranges a network of hydrogen bonds which leads to a large conformational change of the protein and dissociation from DNA. MosR has been shown previously to play an important role on survival of the bacterium in the macrophage. In this study we show that the main role of MosR is to upregulate expression of rv1050 (a putative exported oxidoreductase that has not yet been characterized) in response to oxidants and propose that it is through this role that MosR contributes to the bacterium survival in the macrophage. The oxidation-sensing regulator (MosR) is a new redox dependent transcription factor in Mycobacterium tuberculosis.,Brugarolas P, Movahedzadeh F, Wang Y, Zhang N, Bartek IL, Gao YN, Voskuil MI, Franzblau SG, He C J Biol Chem. 2012 Sep 18. PMID:22992749[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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