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母体因素对小鼠植入前胚胎发育的调控。

Maternal factors regulating preimplantation development in mice.

机构信息

Laboratory of Cellular and Developmental Biology, NIDDK, National Institutes of Health, Bethesda, MD, United States.

出版信息

Curr Top Dev Biol. 2020;140:317-340. doi: 10.1016/bs.ctdb.2019.10.006. Epub 2019 Nov 19.

DOI:10.1016/bs.ctdb.2019.10.006
PMID:32591079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8394711/
Abstract

Mammalian embryogenesis depends on maternal factors accumulated in eggs prior to fertilization and on placental transfers later in gestation. In this review, we focus on initial events when the organism has insufficient newly synthesized embryonic factors to sustain development. These maternal factors regulate preimplantation embryogenesis both uniquely in pronuclear formation, genome reprogramming and cell fate determination and more universally in regulating cell division, transcription and RNA metabolism. Depletion, disruption or inappropriate persistence of maternal factors can result in developmental defects in early embryos. To better understand the origins of these maternal effects, we include oocyte maturation processes that are responsible for their production. We focus on recent publications and reference comprehensive reviews that include earlier scientific literature of early mouse development.

摘要

哺乳动物胚胎发生依赖于受精前卵子中积累的母体因子和妊娠后期胎盘的转运。在这篇综述中,我们重点关注当生物体没有足够新合成的胚胎因子来维持发育时的初始事件。这些母体因子在原核形成、基因组重编程和细胞命运决定方面独特地调节着胚胎的着床前发育,在调节细胞分裂、转录和 RNA 代谢方面也具有普遍性。母体因子的耗尽、破坏或不适当的持续存在可能导致早期胚胎发育缺陷。为了更好地理解这些母体效应的起源,我们包括了负责其产生的卵母细胞成熟过程。我们重点关注最近的出版物,并参考了包括早期小鼠发育在内的更广泛的科学文献的综合评论。

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Maternal factors regulating preimplantation development in mice.母体因素对小鼠植入前胚胎发育的调控。
Curr Top Dev Biol. 2020;140:317-340. doi: 10.1016/bs.ctdb.2019.10.006. Epub 2019 Nov 19.
2
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本文引用的文献

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Cytoplasmic aggregation of DDX1 in developing embryos: Early embryonic lethality associated with Ddx1 knockout.DDX1 在发育胚胎中的细胞质聚集:与 Ddx1 敲除相关的早期胚胎致死。
Dev Biol. 2019 Nov 15;455(2):420-433. doi: 10.1016/j.ydbio.2019.07.014. Epub 2019 Jul 19.
2
Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo Development.多形性腺瘤基因 1 对于合子基因组激活和早期胚胎发育是必需的。
Sci Rep. 2019 Jun 10;9(1):8411. doi: 10.1038/s41598-019-44882-0.
3
Loss of DUX causes minor defects in zygotic genome activation and is compatible with mouse development.DUX 的缺失导致合子基因组激活中的轻微缺陷,并且与小鼠的发育兼容。
Nat Genet. 2019 Jun;51(6):947-951. doi: 10.1038/s41588-019-0418-7. Epub 2019 May 27.
4
Anchoring cortical granules in the cortex ensures trafficking to the plasma membrane for post-fertilization exocytosis.将皮质颗粒锚定在皮质中可确保其运输到质膜,以进行受精后的胞吐作用。
Nat Commun. 2019 May 22;10(1):2271. doi: 10.1038/s41467-019-10171-7.
5
Maintenance of CTCF- and Transcription Factor-Mediated Interactions from the Gametes to the Early Mouse Embryo.从配子到早期小鼠胚胎中维持 CTCF 和转录因子介导的相互作用。
Mol Cell. 2019 Jul 11;75(1):154-171.e5. doi: 10.1016/j.molcel.2019.04.014. Epub 2019 May 2.
6
A slow transcription rate causes embryonic lethality and perturbs kinetic coupling of neuronal genes.转录速度缓慢会导致胚胎致死,并扰乱神经元基因的动力学偶联。
EMBO J. 2019 May 2;38(9). doi: 10.15252/embj.2018101244. Epub 2019 Apr 15.
7
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EMBO J. 2018 Dec 14;37(24). doi: 10.15252/embj.201899333. Epub 2018 Nov 26.
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EMBO J. 2018 Sep 14;37(18). doi: 10.15252/embj.201898981. Epub 2018 Aug 14.
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Aging Cell. 2018 Aug;17(4):e12789. doi: 10.1111/acel.12789. Epub 2018 May 29.