TY - JOUR TI - Dual histone methyl reader ZCWPW1 facilitates repair of meiotic double strand breaks in male mice AU - Mahgoub, Mohamed AU - Paiano, Jacob AU - Bruno, Melania AU - Wu, Wei AU - Pathuri, Sarath AU - Zhang, Xing AU - Ralls, Sherry AU - Cheng, Xiaodong AU - Nussenzweig, André AU - Macfarlan, Todd S A2 - de Massy, Bernard A2 - Tyler, Jessica K A2 - de Massy, Bernard VL - 9 PY - 2020 DA - 2020/04/30 SP - e53360 C1 - eLife 2020;9:e53360 DO - 10.7554/eLife.53360 UR - https://doi.org/10.7554/eLife.53360 AB - Meiotic crossovers result from homology-directed repair of DNA double-strand breaks (DSBs). Unlike yeast and plants, where DSBs are generated near gene promoters, in many vertebrates DSBs are enriched at hotspots determined by the DNA binding activity of the rapidly evolving zinc finger array of PRDM9 (PR domain zinc finger protein 9). PRDM9 subsequently catalyzes tri-methylation of lysine 4 and lysine 36 of Histone H3 in nearby nucleosomes. Here, we identify the dual histone methylation reader ZCWPW1, which is tightly co-expressed during spermatogenesis with Prdm9, as an essential meiotic recombination factor required for efficient repair of PRDM9-dependent DSBs and for pairing of homologous chromosomes in male mice. In sum, our results indicate that the evolution of a dual histone methylation writer/reader (PRDM9/ZCWPW1) system in vertebrates remodeled genetic recombination hotspot selection from an ancestral static pattern near genes towards a flexible pattern controlled by the rapidly evolving DNA binding activity of PRDM9. KW - ZCWPW1 KW - PRDM9 KW - END-seq KW - co-evolution KW - dual histone reader KW - meiotic recombination JF - eLife SN - 2050-084X PB - eLife Sciences Publications, Ltd ER -