Structural basis of the mycobacterial stress-response RNA polymerase auto-inhibition via oligomerization

Nat Commun. 2023 Jan 30;14(1):484. doi: 10.1038/s41467-023-36113-y.

Abstract

Self-assembly of macromolecules into higher-order symmetric structures is fundamental for the regulation of biological processes. Higher-order symmetric structure self-assembly by the gene expression machinery, such as bacterial DNA-dependent RNA polymerase (RNAP), has never been reported before. Here, we show that the stress-response σB factor from the human pathogen, Mycobacterium tuberculosis, induces the RNAP holoenzyme oligomerization into a supramolecular complex composed of eight RNAP units. Cryo-electron microscopy revealed a pseudo-symmetric structure of the RNAP octamer in which RNAP protomers are captured in an auto-inhibited state and display an open-clamp conformation. The structure shows that σB is sequestered by the RNAP flap and clamp domains. The transcriptional activator RbpA prevented octamer formation by promoting the initiation-competent RNAP conformation. Our results reveal that a non-conserved region of σ is an allosteric controller of transcription initiation and demonstrate how basal transcription factors can regulate gene expression by modulating the RNAP holoenzyme assembly and hibernation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / metabolism
  • Cryoelectron Microscopy
  • DNA-Directed RNA Polymerases* / metabolism
  • Holoenzymes / metabolism
  • Humans
  • Mycobacterium tuberculosis* / genetics
  • Sigma Factor* / metabolism
  • Transcription Factors / metabolism
  • Transcription, Genetic

Substances

  • Bacterial Proteins
  • DNA-Directed RNA Polymerases
  • Holoenzymes
  • Sigma Factor
  • Transcription Factors