4.5 Review

Regulation of transcription by eukaryotic-like serine-threonine kinases and phosphatases in Gram-positive bacterial pathogens

Journal

VIRULENCE
Volume 5, Issue 8, Pages 863-885

Publisher

TAYLOR & FRANCIS INC
DOI: 10.4161/21505594.2014.983404

Keywords

bacteria; infection; phosphorylation; serine threonine kinase; serine threonine phosphatase; transcription; TCS; two-component signaling; OCS; one-component signaling; eSTK; eukaryotic-like serine-threonine kinase; eSTP; eukaryotic-like serine-threonine phosphatase; PASTA; penicillin-binding protein and Ser; Thr kinase associated; REC; receiver; wHTH; winged helix-turn-helix; PTM; posttranslational modification; PPM; protein phosphatase metal binding; ROS; reactive oxygen species

Funding

  1. Imperial College London Department of Medicine
  2. Medical Research Council
  3. MRC [MR/J006874/1] Funding Source: UKRI
  4. Medical Research Council [MR/J006874/1B, MR/J006874/1] Funding Source: researchfish

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Bacterial eukaryotic-like serine threonine kinases (eSTKs) and serine threonine phosphatases (eSTPs) have emerged as important signaling elements that are indispensable for pathogenesis. Differing considerably from their histidine kinase counterparts, few eSTK genes are encoded within the average bacterial genome, and their targets are pleiotropic in nature instead of exclusive. The growing list of important eSTK/P substrates includes proteins involved in translation, cell division, peptidoglycan synthesis, antibiotic tolerance, resistance to innate immunity and control of virulence factors. Recently it has come to light that eSTK/Ps also directly modulate transcriptional machinery in many microbial pathogens. This novel form of regulation is now emerging as an additional means by which bacteria can alter their transcriptomes in response to host-specific environmental stimuli. Here we focus on the ability of eSTKs and eSTPs in Gram-positive bacterial pathogens to directly modulate transcription, the known mechanistic outcomes of these modifications, and their roles as an added layer of complexity in controlling targeted RNA synthesis to enhance virulence potential.

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