The histone modification reader ZCWPW1 is required for meiosis prophase I in male but not in female mice.

Abstract

Meiosis is a specialized type of cell division that creates haploid germ cells and ensures their genetic diversity through homologous recombination. We show that the H3K4me3 reader ZCWPW1 is specifically required for meiosis prophase I progression in male but not in female germ cells in mice. Loss of <i>Zcwpw1</i> in male mice caused a complete failure of synapsis, resulting in meiotic arrest at the zygotene to pachytene stage, accompanied by incomplete DNA double-strand break repair and lack of crossover formation, leading to male infertility. In oocytes, deletion of <i>Zcwpw1</i> only somewhat slowed down meiosis prophase I progression; <i>Zcwpw1^-/-</i> oocytes were able to complete meiosis, and <i>Zcwpw1^-/-</i> female mice had normal fertility until mid-adulthood. We conclude that the H3K4me3 reader ZCWPW1 is indispensable for meiosis synapsis in males but is dispensable for females. Our results suggest that ZCWPW1 may represent a previously unknown, sex-dependent epigenetic regulator of germ cell meiosis in mammals.