Homologous recombination within repetitive DNA

Curr Opin Genet Dev. 2021 Dec:71:143-153. doi: 10.1016/j.gde.2021.08.005. Epub 2021 Aug 28.

Abstract

Many microsatellite DNA sequences are able to form non-B form DNA secondary structures, such as hairpin loops, cruciforms, triplex DNA or G-quadruplexes. These DNA structures can form a significant impediment to DNA replication and repair, leading to DNA nicks, gaps, and breaks, which can be repaired by homologous recombination (HR). Recent work understanding HR at structure-forming repeats has focused on genetic requirements for replication fork restart, break induced replication (BIR) at broken forks, recombination during and after relocalization of breaks or stalled forks to the nuclear periphery, and how repair pathway choice and kinetics are navigated in the presence of a repeat tract. In this review, we summarize recent developments that illuminate the role of recombination in repairing DNA damage or causing tract length changes within repetitive DNA and its role in maintaining genome stability.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • DNA / chemistry
  • DNA Damage
  • DNA Repair / genetics
  • DNA Replication* / genetics
  • Genomic Instability / genetics
  • Homologous Recombination* / genetics
  • Humans

Substances

  • DNA