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MSH2 stimulates interfering and inhibits non-interfering crossovers in response to genetic polymorphism.

Julia DluzewskaWojciech DziegielewskiMaja Szymanska-LejmanMonika GazeckaIan R HendersonJames D HigginsPiotr A Ziolkowski
Published in: Nature communications (2023)
Meiotic crossovers can be formed through the interfering pathway, in which one crossover prevents another from forming nearby, or by an independent non-interfering pathway. In Arabidopsis, local sequence polymorphism between homologs can stimulate interfering crossovers in a MSH2-dependent manner. To understand how MSH2 regulates crossovers formed by the two pathways, we combined Arabidopsis mutants that elevate non-interfering crossovers with msh2 mutants. We demonstrate that MSH2 blocks non-interfering crossovers at polymorphic loci, which is the opposite effect to interfering crossovers. We also observe MSH2-independent crossover inhibition at highly polymorphic sites. We measure recombination along the chromosome arms in lines differing in patterns of heterozygosity and observe a MSH2-dependent crossover increase at the boundaries between heterozygous and homozygous regions. Here, we show that MSH2 is a master regulator of meiotic DSB repair in Arabidopsis, with antagonistic effects on interfering and non-interfering crossovers, which shapes the crossover landscape in relation to interhomolog polymorphism.
Keyphrases
  • transcription factor
  • randomized controlled trial
  • gene expression
  • genome wide
  • double blind
  • dna methylation
  • single cell
  • study protocol
  • cell wall