Division of Reproductive Sciences, Division of Developmental Biology, Perinatal Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH45229, USA.
Department of Molecular Biology, Keio University School of Medicine, Tokyo160-8582, Japan.
Nucleic Acids Res. 2023 Jul 21;51(13):6668-6683. doi: 10.1093/nar/gkad479.
Sperm chromatin retains small amounts of histones, and chromatin states of sperm mirror gene expression programs of the next generation. However, it remains largely unknown how paternal epigenetic information is transmitted through sperm chromatin. Here, we present a novel mouse model of paternal epigenetic inheritance, in which deposition of Polycomb repressive complex 2 (PRC2) mediated-repressive H3K27me3 is attenuated in the paternal germline. By applying modified methods of assisted reproductive technology using testicular sperm, we rescued infertility of mice missing Polycomb protein SCML2, which regulates germline gene expression by establishing H3K27me3 on bivalent promoters with other active marks H3K4me2/3. We profiled epigenomic states (H3K27me3 and H3K4me3) of testicular sperm and epididymal sperm, demonstrating that the epididymal pattern of the sperm epigenome is already established in testicular sperm and that SCML2 is required for this process. In F1 males of X-linked Scml2-knockout mice, which have a wild-type genotype, gene expression is dysregulated in the male germline during spermiogenesis. These dysregulated genes are targets of SCML2-mediated H3K27me3 in F0 sperm. Further, dysregulation of gene expression was observed in the mutant-derived wild-type F1 preimplantation embryos. Together, we present functional evidence that the classic epigenetic regulator Polycomb mediates paternal epigenetic inheritance through sperm chromatin.
精子染色质保留少量组蛋白,精子的染色质状态反映了下一代的基因表达程序。然而,父系表观遗传信息如何通过精子染色质传递仍然很大程度上未知。在这里,我们提出了一种新的父系表观遗传遗传模型,其中多梳抑制复合物 2 (PRC2) 介导的抑制性 H3K27me3 在父系生殖细胞中减弱。通过应用睾丸精子辅助生殖技术的改良方法,我们挽救了缺失多梳蛋白 SCML2 的小鼠的不育症,SCML2 通过在具有其他活性标记 H3K4me2/3 的双价启动子上建立 H3K27me3 来调节生殖细胞基因表达。我们对睾丸精子和附睾精子的表观基因组状态(H3K27me3 和 H3K4me3)进行了分析,结果表明,附睾精子的表观基因组模式已经在睾丸精子中建立,而 SCML2 是这个过程所必需的。在 X 连锁 Scml2 敲除小鼠的 F1 雄性中,其基因型为野生型,在精子发生过程中,生殖细胞中的基因表达出现失调。这些失调的基因是 F0 精子中 SCML2 介导的 H3K27me3 的靶标。此外,在突变体衍生的野生型 F1 着床前胚胎中观察到基因表达失调。总之,我们提供了功能证据表明,经典的表观遗传调节剂 Polycomb 通过精子染色质介导父系表观遗传遗传。