Identification of a promoter motif regulating the major DNA damage response mechanism of Mycobacterium tuberculosis

FEMS Microbiol Lett. 2004 Sep 1;238(1):57-63. doi: 10.1016/j.femsle.2004.07.017.

Abstract

The principal response of many bacteria to DNA damage is mediated by a mechanism dependent on the LexA and RecA proteins. However, Mycobacterium tuberculosis was recently reported to regulate a majority of DNA repair genes independently of RecA and LexA, suggesting that an unknown RecA/LexA-independent mechanism controls the major DNA damage response pathway in this organism. Here we have identified a motif tTGTCRgtg-8nt-TAnnnT that defines a novel RecA/LexA-independent promoter (RecA-NDp) of M. tuberculosis. Furthermore, we show that the RecA-NDp type of promoter precedes DNA repair genes in other Actinomycetales.

MeSH terms

  • Actinomycetales / genetics
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Bacterial Proteins / physiology
  • Base Sequence
  • Consensus Sequence
  • DNA Damage*
  • DNA Repair / genetics*
  • Gene Expression Regulation, Bacterial*
  • Humans
  • Molecular Sequence Data
  • Mycobacterium tuberculosis / genetics*
  • Mycobacterium tuberculosis / metabolism*
  • Promoter Regions, Genetic*
  • Rec A Recombinases / genetics
  • Rec A Recombinases / metabolism
  • Regulon
  • Sequence Alignment
  • Serine Endopeptidases / genetics
  • Serine Endopeptidases / metabolism
  • Sigma Factor / physiology

Substances

  • Bacterial Proteins
  • LexA protein, Bacteria
  • Sigma Factor
  • Rec A Recombinases
  • Serine Endopeptidases