Xu Chengpeng, Qin Dandan, Lu Xukun, Qi Qianqian, Wu Yu, Wang Qizhi, Han Zhuo, Nie Xiaoqing, Jiang Yongmei, Deng Dong, Xie Wei, Gao Zheng, Li Lei
State Key Laboratory of Organ Regeneration and Reconstruction, Beijing Institute for Stem Cell and Regenerative Medicine, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
University of Chinese Academy of Sciences, Chinese Academy of Sciences, Beijing, China.
Nat Struct Mol Biol. 2025 Apr 17. doi: 10.1038/s41594-025-01538-0.
How cytoplasmic regulators control nuclear events in mammalian oocytes and early embryos remains largely enigmatic. We previously identified a subcortical maternal complex (SCMC) that specifically resides in the cytoplasm of mammalian oocytes and early embryos but is also involved in nuclear events. Nevertheless, how the cytoplasmic SCMC exerts its role in nuclear processes remains unknown. In this study, we unveil SPIN1, a histone methylation reader, as a novel member of the SCMC. The SCMC component FILIA tightly regulates the expression and cytoplasmic localization of SPIN1 through direct interaction. When the expression of FILIA is decreased because of genetic mutations of SCMC genes, SPIN1 expression is dramatically reduced but the residual SPIN1 translocates into the nucleus. The abnormal nuclear presence of SPIN1 impairs H3K4me3 reprogramming, zygotic genome activation and physiological embryonic development. Inhibiting the interaction between SPIN1 and H3K4me3 partially rescues the abnormal phenotype in FILIA-null embryos. Mechanistically, SPIN1 partially perturbs the demethylation process by competing with KDM5B for binding to H3K4me3. Collectively, our work highlights the complexity of the mammalian SCMC and oocyte-to-embryo transition, revealing an intricate regulatory mechanism that facilitates the smooth progression of this process.
细胞质调节因子如何控制哺乳动物卵母细胞和早期胚胎中的核事件在很大程度上仍然是个谜。我们之前鉴定出一种皮质下母体复合体(SCMC),它特异性地存在于哺乳动物卵母细胞和早期胚胎的细胞质中,但也参与核事件。然而,细胞质中的SCMC如何在核过程中发挥作用仍然未知。在这项研究中,我们揭示了一种组蛋白甲基化阅读器SPIN1,它是SCMC的一个新成员。SCMC组分FILIA通过直接相互作用紧密调节SPIN1的表达和细胞质定位。当由于SCMC基因的基因突变导致FILIA表达降低时,SPIN1的表达会显著减少,但残余的SPIN1会转运到细胞核中。SPIN1在细胞核中的异常存在会损害H3K4me3重编程、合子基因组激活和胚胎的正常发育。抑制SPIN1与H3K4me3之间的相互作用可部分挽救FILIA基因敲除胚胎中的异常表型。从机制上讲,SPIN1通过与KDM5B竞争结合H3K4me3来部分扰乱去甲基化过程。总的来说,我们的工作突出了哺乳动物SCMC和卵母细胞向胚胎转变的复杂性,揭示了一种复杂的调节机制,有助于这一过程的顺利进行。