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哺乳动物胚胎植入前的基因组折叠和胚胎基因组激活。

Genome folding and zygotic genome activation in mammalian preimplantation embryos.

机构信息

Department of Totipotency, Max Planck Institute of Biochemistry, Martinsried, Munich, Germany.

Department of Totipotency, Max Planck Institute of Biochemistry, Martinsried, Munich, Germany.

出版信息

Curr Opin Genet Dev. 2024 Dec;89:102268. doi: 10.1016/j.gde.2024.102268. Epub 2024 Oct 9.

Abstract

The totipotent one-cell embryo, or zygote, gives rise to all germ layers and extraembryonic tissues that culminate in the development of a new organism. A zygote is produced at fertilisation by the fusion of differentiated germ cells, egg and sperm. The chromatin of parental genomes is reprogrammed and spatially reorganised in the early embryo. The 3D chromatin organisation is established de novo after fertilisation by a cohesin-dependent mechanism of loop extrusion that forms chromatin loops and topologically associating domains (TADs). Strengthening of TAD insulation is concomitant with the transcriptional 'awakening' of the embryo known as zygotic genome activation (ZGA). Whether and how these processes are causally linked remains poorly understood. In this review, we discuss recent findings of 3D chromatin organisation in mammalian gametes and embryos and how these are potentially related to ZGA.

摘要

全能的单细胞胚胎,或受精卵,产生所有的胚层和胚胎外组织,最终发育成一个新的生物体。受精卵是由分化的生殖细胞、卵子和精子融合而在受精时产生的。亲本基因组的染色质在早期胚胎中被重新编程和空间重组。在受精后,通过依赖于黏连蛋白的环挤出机制形成染色质环和拓扑关联域(TAD),从头建立三维染色质组织。TAD 绝缘的增强伴随着胚胎转录“觉醒”,即合子基因组激活(ZGA)。这些过程是否以及如何因果相关仍知之甚少。在这篇综述中,我们讨论了哺乳动物配子和胚胎中三维染色质组织的最新发现,以及这些发现如何与 ZGA 相关。

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