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Extensive and orderly reprogramming of genome-wide chromatin modifications associated with specification and early development of germ cells in mice

机译:广泛和有序地重编程与小鼠生殖细胞的规格和早期发育有关的全基因组染色质修饰

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Induction of mouse germ cells occurs from the proximal epiblast at around embryonic day (E) 7.0. These germ cells then migrate to, and enter the gonads at about E10.5 after which they undergo epigenetic reprogramming including erasure of parental imprints. However, the epigenetic properties acquired by nascent germ cells and the potential remodeling of these epigenetic marks in the subsequent migratory period have been largely unexplored. Here we have used immunohistochemistry to examine several genome-wide epigenetic modifications occurring in germ cells from their specification to their colonization of the genital ridges. We show that at around E8.0, germ cells concomitantly and significantly reduce H3-K9 dimethylation and DNA methylation, two major repressive modifications for gene expression. These events are preceded by the transient loss of all the DNA methyltransferases from their nuclei. By contrast, germ cells substantially increase the levels of H3-K27 trimethylation, another repressive modification with more plasticity, at E8.5-9.0 and maintain this state until at least E12.5. H3-K4 methylation and H3-K9 acetylation, modifications associated with transcriptionally permissive/active chromatin, are similar in germ and surrounding somatic cells but germ cells transiently increase these marks sharply upon their entry into the genital ridge. H3-K9 trimethylation, a hallmark of centromeric heterochromatin, is kept relatively constant during the periods examined. We suggest that this orderly and extensive epigenetic reprogramming in premigratory and migratory germ cells might be necessary for their reacquisition of underlying totipotency, for subsequent specific epigenetic remodeling, including the resetting of parental imprints, and for the production of gametes with an appropriate epigenotype for supporting normal development. (C) 2004 Elsevier Inc. All rights reserved.
机译:小鼠生殖细胞的诱导在胚胎日(E)7.0左右从近端上皮细胞发生。这些生殖细胞然后迁移到性腺,并在大约E10.5处进入性腺,之后它们进行表观遗传重编程,包括擦除父母的印记。然而,尚未充分探索新生生殖细胞获得的表观遗传特性以及这些表观遗传标记在随后的迁徙期中的潜在重塑。在这里,我们已经使用免疫组织化学检查了生殖细胞中发生的数种全基因组表观遗传修饰,从其规格到生殖脊定植。我们显示,在E8.0左右,生殖细胞伴随并显着减少H3-K9二甲基化和DNA甲基化,这是基因表达的两个主要抑制性修饰。在这些事件发生之前,所有DNA甲基转移酶都从其核中暂时丢失。相比之下,生殖细胞在E8.5-9.0时会显着提高H3-K27三甲基化的水平,这是另一种具有更多可塑性的阻遏性修饰,并且至少在E12.5之前保持这种状态。 H3-K4甲基化和H3-K9乙酰化(与转录许可/活性染色质相关的修饰)在生殖细胞和周围的体细胞中相似,但是生殖细胞在进入生殖器ridge部后会暂时急剧增加这些标记。 H3-K9三甲基化是着丝粒异染色质的标志,在检查期间保持相对恒定。我们建议在迁徙和迁徙的生殖细胞中进行这种有序且广泛的表观遗传重编程对于其潜在的全能性的重新获得,随后的特定表观遗传重塑(包括父母亲印记的重置)以及具有适当表观基因型的配子的生产支持可能是必要的。正常发展。 (C)2004 Elsevier Inc.保留所有权利。

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