Structural analysis of alternate sigma factor ComX with RpoC, RpoB and its cognate CIN promoter reveals a distinctive promoter melting mechanism

J Biomol Struct Dyn. 2022 Sep;40(14):6272-6285. doi: 10.1080/07391102.2021.1882338. Epub 2021 Feb 8.

Abstract

Alternate sigma factors play a major role in the survival of pathogenic bacteria such as Streptococcus pyogenes in adverse environment conditions. Stress induced sigma factors mediate gene expression under conditions of pathogenesis, dormancy and unusual environmental cues. In the present work, ComX, an alternate sigma factor from S. pyogenes has been characterized. The structures of ComX, RpoB β subunit and RpoC β' subunit of RNA polymerase have been predicted using comparative and homology modelling respectively and validated. Attempts have been made to study RpoB-RpoC-ComX complex interactions with Double Strand (DS) and Single Strand (SS) promoter regions. Stability of these complexes and the promoter melting mechanism have been analysed using Molecular Dynamic (MD) simulations. This study suggests that ComX, although identifies promoter analogous to the alternate sigma factor SigH of M. tuberculosis, follows a distinctive promoter flip out mechanism.Communicated by Ramaswamy H. Sarma.

Keywords: Alternate sigma factor; RNA polymerase; protein-protein docking; protein–DNA docking.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / chemistry
  • Bacterial Proteins / metabolism
  • DNA-Directed RNA Polymerases / chemistry*
  • DNA-Directed RNA Polymerases / metabolism
  • Gene Expression Regulation, Bacterial
  • Mycobacterium tuberculosis / genetics
  • Promoter Regions, Genetic
  • Sigma Factor / chemistry
  • Sigma Factor / genetics
  • Streptococcus pyogenes / chemistry*
  • Streptococcus pyogenes / metabolism
  • Transcription Factors / chemistry
  • Transcription Factors / metabolism
  • Transcription, Genetic

Substances

  • Bacterial Proteins
  • ComX protein, Streptococcus
  • Sigma Factor
  • Transcription Factors
  • DNA-Directed RNA Polymerases