DNA sequence-mediated, evolutionarily rapid redistribution of meiotic recombination hotspots

Genetics. 2011 Nov;189(3):685-94. doi: 10.1534/genetics.111.134130.

Abstract

Hotspots regulate the position and frequency of Spo11 (Rec12)-initiated meiotic recombination, but paradoxically they are suicidal and are somehow resurrected elsewhere in the genome. After the DNA sequence-dependent activation of hotspots was discovered in fission yeast, nearly two decades elapsed before the key realizations that (A) DNA site-dependent regulation is broadly conserved and (B) individual eukaryotes have multiple different DNA sequence motifs that activate hotspots. From our perspective, such findings provide a conceptually straightforward solution to the hotspot paradox and can explain other, seemingly complex features of meiotic recombination. We describe how a small number of single-base-pair substitutions can generate hotspots de novo and dramatically alter their distribution in the genome. This model also shows how equilibrium rate kinetics could maintain the presence of hotspots over evolutionary timescales, without strong selective pressures invoked previously, and explains why hotspots localize preferentially to intergenic regions and introns. The model is robust enough to account for all hotspots of humans and chimpanzees repositioned since their divergence from the latest common ancestor.

Publication types

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

MeSH terms

  • Animals
  • Base Pairing
  • Base Sequence
  • DNA / genetics*
  • Evolution, Molecular*
  • Humans
  • Meiosis / genetics*
  • Models, Genetic
  • Recombination, Genetic*
  • Selection, Genetic

Substances

  • DNA