Inhibition of the DevSR Two-Component System by Overexpression of Mycobacterium tuberculosis PknB in Mycobacterium smegmatis

Mol Cells. 2017 Sep 30;40(9):632-642. doi: 10.14348/molcells.2017.0076. Epub 2017 Aug 25.

Abstract

The DevSR (DosSR) two-component system, which is a major regulatory system involved in oxygen sensing in mycobacteria, plays an important role in hypoxic induction of many genes in mycobacteria. We demonstrated that overexpression of the kinase domain of Mycobacterium tuberculosis (Mtb) PknB inhibited transcriptional activity of the DevR response regulator in Mycobacterium smegmatis and that this inhibitory effect was exerted through phosphorylation of DevR on Thr180 within its DNA-binding domain. Moreover, the purified kinase domain of Mtb PknB significantly phosphorylated RegX3, NarL, KdpE, TrcR, DosR, and MtrA response regulators of Mtb that contain the Thr residues corresponding to Thr180 of DevR in their DNA-binding domains, implying that transcriptional activities of these response regulators might also be inhibited when the kinase domain of PknB is overexpressed.

Keywords: DevSR; Ser/Thr protein kinase; mycobacterium; two-component system.

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Cell Hypoxia / genetics*
  • DNA-Binding Proteins
  • Gene Expression Regulation, Bacterial / genetics
  • Humans
  • Mycobacterium smegmatis / genetics*
  • Mycobacterium smegmatis / metabolism
  • Mycobacterium tuberculosis / genetics*
  • Mycobacterium tuberculosis / metabolism
  • Mycobacterium tuberculosis / pathogenicity
  • Oxygen / chemistry
  • Oxygen / metabolism
  • Phosphorylation
  • Protamine Kinase / genetics
  • Protamine Kinase / metabolism
  • Protein Kinases / genetics
  • Protein Kinases / metabolism
  • Protein Serine-Threonine Kinases / genetics*
  • Protein Serine-Threonine Kinases / metabolism
  • Tuberculosis / genetics
  • Tuberculosis / microbiology

Substances

  • Bacterial Proteins
  • DNA-Binding Proteins
  • DosR protein, Mycobacterium tuberculosis
  • Protein Kinases
  • PknB protein, Mycobacterium tuberculosis
  • DevS protein, Mycobacterium tuberculosis
  • Protamine Kinase
  • Protein Serine-Threonine Kinases
  • Oxygen