期刊
GENES & DEVELOPMENT
卷 29, 期 20, 页码 2183-2202出版社
COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.270876.115
关键词
meiosis; crossover; hot spots; epigenetics; DNA methylation; centromeres
资金
- Broodbank Fellowship
- Royal Society University Research Fellowship
- Gatsby Charitable Foundation [GAT2962]
- Biotechnology and Biological Sciences Research Council [BB/L006847/1]
- BBSRC [BB/K007882/1, BB/L006847/1, BB/M004937/1] Funding Source: UKRI
- Biotechnology and Biological Sciences Research Council [BB/M004937/1, BB/K007882/1, BB/L006847/1] Funding Source: researchfish
During meiosis, homologous chromosomes undergo crossover recombination, which is typically concentrated in narrow hot spots that are controlled by genetic and epigenetic information. Arabidopsis chromosomes are highly DNA methylated in the repetitive centromeres, which are also crossover-suppressed. Here we demonstrate that RNA-directed DNA methylation is sufficient to locally silence Arabidopsis euchromatic crossover hot spots and is associated with increased nucleosome density and H3K9me2. However, loss of CG DNA methylation maintenance in met1 triggers epigenetic crossover remodeling at the chromosome scale, with pericentromeric decreases and euchromatic increases in recombination. We used recombination mutants that alter interfering and noninterfering crossover repair pathways (fancm and zip4) to demonstrate that remodeling primarily involves redistribution of interfering crossovers. Using whole-genome bisulfite sequencing, we show that crossover remodeling is driven by loss ofCG methylation within the centromeric regions. Using cytogenetics, we profiled meiotic DNA double-strand break (DSB) foci in met1 and found them unchanged relative to wild type. We propose that met1 chromosome structure is altered, causing centromere-proximal DSBs to be inhibited frommaturation into interfering crossovers. These data demonstrate that DNA methylation is sufficient to silence crossover hot spots and plays a key role in establishing domains of meiotic recombination along chromosomes.
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