Tuning the Mycobacterium tuberculosis Alternative Sigma Factor SigF through the Multidomain Regulator Rv1364c and Osmosensory Kinase Protein Kinase D
Author(s) -
Richa Misra,
Dilip Me,
Gunjan Arora,
R Virmani,
Mohita Gaur,
Saba Naz,
Neetika Jaisinghani,
Asani Bhaduri,
Ankur Bothra,
Abhijit Maji,
Anshika Singhal,
Preeti Karwal,
Christian Hentschker,
Dörte Becher,
Vivek Rao,
Vinay Kumar Nandicoori,
Sheetal Gandotra,
Yogendra Singh
Publication year - 2019
Publication title -
journal of bacteriology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.652
H-Index - 246
eISSN - 1067-8832
pISSN - 0021-9193
DOI - 10.1128/jb.00725-18
Subject(s) - sigma factor , regulon , biology , mycobacterium tuberculosis , virulence factor , autophosphorylation , microbiology and biotechnology , regulator , phosphorylation , transcription factor , rna polymerase , protein kinase a , biochemistry , virulence , gene , rna , medicine , tuberculosis , pathology
Mycobacterium tuberculosis , capable of latently infecting the host and causing aggressive tissue damage during active tuberculosis, is endowed with a complex regulatory capacity built of several sigma factors, protein kinases, and phosphatases. These proteins regulate expression of genes that allow the bacteria to adapt to various host-derived stresses, like nutrient starvation, acidic pH, and hypoxia. The cross talk between these systems is not well understood. SigF is one such regulator of gene expression that helpsM. tuberculosis to adapt to stresses and imparts virulence. This work provides evidence for its inhibition by the multidomain regulator Rv1364c and activation by the kinase PknD. The coexistence of negative and positive regulators of SigF in pathogenic bacteria reveals an underlying requirement for tight control of virulence factor expression.
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