Mei Hailiang, Hayashi Ryoya, Kozuka Chisayo, Kumon Mami, Koseki Haruhiko, Inoue Azusa
Laboratory for Epigenome Inheritance, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Tokyo Metropolitan University, Hachioji, Japan.
Nat Struct Mol Biol. 2025 Jun 13. doi: 10.1038/s41594-025-01573-x.
Mammalian oocytes establish a unique landscape of histone modifications, some of which are inherited by early embryos. How histone variants shape the maternal histone landscape remains unknown. Here we map histone H2A variants in mouse fully grown oocytes (FGOs) and find that H2A.Z forms broad domains across intergenic regions, along non-canonical H3K4me3 (ncH3K4me3). During oocyte growth, H2A.Z progressively transitions from an active promoter-rich, canonical distribution to a non-canonical broad distribution (ncH2A.Z). Depletion of H2A.Z in oocytes partially impairs ncH3K4me3 formation and causes severe defects in meiotic progression, which resemble Mll2-knockout oocytes. Conversely, depletion of ncH3K4me3 by Mll2 knockout also causes a reduction of ncH2A.Z in FGOs. Thus, our study suggests that ncH2A.Z and ncH3K4me3 reinforce each other to form functional oocytes.
哺乳动物卵母细胞建立了独特的组蛋白修饰格局,其中一些修饰会被早期胚胎继承。组蛋白变体如何塑造母源组蛋白格局仍不清楚。在这里,我们绘制了小鼠完全成熟卵母细胞(FGOs)中的组蛋白H2A变体图谱,发现H2A.Z在基因间区域形成广泛结构域,沿着非经典H3K4me3(ncH3K4me3)分布。在卵母细胞生长过程中,H2A.Z逐渐从富含活性启动子的经典分布转变为非经典的广泛分布(ncH2A.Z)。卵母细胞中H2A.Z的缺失部分损害了ncH3K4me3的形成,并导致减数分裂进程出现严重缺陷,这与Mll2基因敲除的卵母细胞相似。相反,通过敲除Mll2来消耗ncH3K4me3也会导致FGOs中ncH2A.Z减少。因此,我们的研究表明,ncH2A.Z和ncH3K4me3相互加强,以形成功能正常的卵母细胞。