Urli Teresa, Greenberg Maxim V C
Université Paris Cité, CNRS, Institut Jacques Monod, Paris, France.
PLoS Genet. 2025 Sep 15;21(9):e1011854. doi: 10.1371/journal.pgen.1011854. eCollection 2025 Sep.
In mammals, repression of germline-specific gene expression is essential for preserving somatic cell identity and preventing disease. Germline gene silencing is often dependent on the presence of promoter 5-cytosine DNA methylation (5meC). Early mammalian development, however, is marked by a dramatic loss of 5meC levels genome-wide. Recent research has highlighted a specialized variant of the Polycomb Repressive Complex 1, PRC1.6, as a key regulator that maintains transient silencing of germline genes in this embryonic window. Eventually, PRC1.6 seems to stimulate the recruitment of de novo DNA methyltransferases (DNMTs), although the precise mechanisms remain to be fully elucidated. Evidence suggests a coordinated epigenetic relay, potentially involving direct protein interactions and shaping the local histone modification landscape. This review explores PRC1.6 as a central epigenetic hub that connects Polycomb repression, histone 3 lysine 9 (H3K9) methylation, and DNA methylation pathways. Unraveling this interplay will provide key insights into the mechanisms that maintain the critical barrier between the germline and the soma, essential not only for proper development but also for preserving somatic cell function and health throughout life.
在哺乳动物中,抑制生殖系特异性基因表达对于维持体细胞特性和预防疾病至关重要。生殖系基因沉默通常依赖于启动子5-胞嘧啶DNA甲基化(5meC)的存在。然而,早期哺乳动物发育的特征是全基因组范围内5meC水平急剧下降。最近的研究强调了多梳抑制复合体1(PRC1)的一个特殊变体PRC1.6,它是在这个胚胎期维持生殖系基因短暂沉默的关键调节因子。最终,PRC1.6似乎会刺激从头DNA甲基转移酶(DNMT)的募集,尽管其精确机制仍有待充分阐明。有证据表明存在一种协调的表观遗传传递,可能涉及直接的蛋白质相互作用并塑造局部组蛋白修饰格局。本综述探讨了PRC1.6作为一个核心表观遗传枢纽,它连接了多梳抑制、组蛋白3赖氨酸9(H3K9)甲基化和DNA甲基化途径。揭示这种相互作用将为维持生殖系和体细胞之间关键屏障的机制提供关键见解,这不仅对正常发育至关重要,而且对终身维持体细胞功能和健康也至关重要。