RT Journal Article SR Electronic T1 Epigenetic activation of meiotic recombination in Arabidopsis centromeres via loss of H3K9me2 and non-CG DNA methylation JF bioRxiv FD Cold Spring Harbor Laboratory SP 160929 DO 10.1101/160929 A1 Charles J. Underwood A1 Kyuha Choi A1 Christophe Lambing A1 Xiaohui Zhao A1 Heïdi Serra A1 Filipe Borges A1 Joe Simorowski A1 Evan Ernst A1 Yannick Jacob A1 Ian R. Henderson A1 Robert A. Martienssen YR 2017 UL http://biorxiv.org/content/early/2017/07/08/160929.abstract AB Eukaryotic centromeres contain the kinetochore, which connects chromosomes to the spindle allowing segregation. During meiosis centromeres are suppressed for crossovers, as recombination in these regions can cause chromosome mis-segregation. Plant centromeres are surrounded by repetitive, transposon-dense heterochromatin that is epigenetically silenced by histone 3 lysine 9 dimethylation (H3K9me2), and DNA methylation in CG and non-CG sequence contexts. Here we show that disruption of Arabidopsis H3K9me2 and non-CG DNA methylation pathways increases meiotic DNA double strand breaks (DSBs) within centromeres, whereas crossovers increase within pericentromeric heterochromatin. Increased pericentromeric crossovers in H3K9me2/non-CG mutants occurs in both inbred and hybrid backgrounds, and involves the interfering crossover repair pathway. Epigenetic activation of recombination may also account for the curious tendency of maize transposon Ds to disrupt CHROMOMETHYLASE3 when launched from proximal loci. Thus H3K9me2 and non-CG DNA methylation exert differential control of meiotic DSB and crossover formation in centromeric and pericentromeric heterochromatin.