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小鼠胚胎和生殖系中基因特异性DNA甲基化的发育模式。

Developmental pattern of gene-specific DNA methylation in the mouse embryo and germ line.

作者信息

Kafri T, Ariel M, Brandeis M, Shemer R, Urven L, McCarrey J, Cedar H, Razin A

机构信息

Department of Cellular Biochemistry, Hebrew University Medical School, Jerusalem, Israel.

出版信息

Genes Dev. 1992 May;6(5):705-14. doi: 10.1101/gad.6.5.705.

Abstract

Methylation patterns of specific genes have been studied by polymerase chain reaction and found to undergo dynamic changes in the germ line and early embryo. Some CpG sites are methylated in sperm DNA and unmodified in mature oocytes, indicating that the parental genomes have differential methylation profiles. These differences, however, are erased by a series of early embryonic demethylation and postblastula remodification events, which serve to reestablish the basic adult methylation pattern prior to organogenesis. During gametogenesis, all of these sites are unmethylated in primordial germ cells but eventually become remodified by 18.5 days postcoitum in both males and females. The final methylation profile of the mature germ cells is then formed by a multistep process of site-specific demethylation events. These results form a basis for the understanding of the biochemical mechanisms and role of DNA methylation in embryonic development.

摘要

通过聚合酶链反应研究了特定基因的甲基化模式,发现其在生殖系和早期胚胎中会发生动态变化。一些CpG位点在精子DNA中被甲基化,而在成熟卵母细胞中未被修饰,这表明亲代基因组具有不同的甲基化谱。然而,这些差异会被一系列早期胚胎去甲基化和囊胚后期重塑事件消除,这些事件有助于在器官发生之前重新建立基本的成年甲基化模式。在配子发生过程中,所有这些位点在原始生殖细胞中都是未甲基化的,但最终在雄性和雌性中都会在交配后18.5天被重塑。成熟生殖细胞的最终甲基化谱是通过位点特异性去甲基化事件的多步骤过程形成的。这些结果为理解DNA甲基化在胚胎发育中的生化机制和作用奠定了基础。

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