Y-family DNA polymerases in Escherichia coli

Trends Microbiol. 2007 Feb;15(2):70-7. doi: 10.1016/j.tim.2006.12.004. Epub 2007 Jan 4.

Abstract

The observation that mutations in the Escherichia coli genes umuC+ and umuD+ abolish mutagenesis induced by UV light strongly supported the counterintuitive notion that such mutagenesis is an active rather than passive process. Genetic and biochemical studies have revealed that umuC+ and its homolog dinB+ encode novel DNA polymerases with the ability to catalyze synthesis past DNA lesions that otherwise stall replication--a process termed translesion synthesis (TLS). Similar polymerases have been identified in nearly all organisms, constituting a new enzyme superfamily. Although typically viewed as unfaithful copiers of DNA, recent studies suggest that certain TLS polymerases can perform proficient and moderately accurate bypass of particular types of DNA damage. Moreover, various cellular factors can modulate their activity and mutagenic potential.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • DNA Damage
  • DNA Polymerase beta / physiology*
  • DNA Repair / physiology
  • DNA-Directed DNA Polymerase / chemistry
  • DNA-Directed DNA Polymerase / genetics
  • DNA-Directed DNA Polymerase / physiology*
  • Escherichia coli / enzymology*
  • Escherichia coli / genetics
  • Escherichia coli Proteins / chemistry
  • Escherichia coli Proteins / physiology*
  • Models, Molecular
  • Mutagenesis / radiation effects
  • Ultraviolet Rays

Substances

  • DinB protein, E coli
  • Escherichia coli Proteins
  • UmuC protein, E coli
  • DNA Polymerase beta
  • DNA-Directed DNA Polymerase
  • UmuD protein, E coli