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胚胎发育中的 DNA 甲基化:ART(辅助生殖技术)的表观遗传学影响。

DNA Methylation in Embryo Development: Epigenetic Impact of ART (Assisted Reproductive Technologies).

机构信息

Physiology of Reproduction Group, University of Murcia, Murcia, Spain.

IMIB-Arrixaca Spain, Murcia, Spain.

出版信息

Bioessays. 2017 Nov;39(11). doi: 10.1002/bies.201700106. Epub 2017 Sep 21.

Abstract

DNA methylation can be considered a component of epigenetic memory with a critical role during embryo development, and which undergoes dramatic reprogramming after fertilization. Though it has been a focus of research for many years, the reprogramming mechanism is still not fully understood. Recent results suggest that absence of maintenance at DNA replication is a major factor, and that there is an unexpected role for TET3-mediated oxidation of 5mC to 5hmC in guarding against de novo methylation. Base-resolution and genome-wide profiling methods are enabling more comprehensive assessments of the extent to which ART might impair DNA methylation reprogramming, and which sequence elements are most vulnerable. Indeed, as we also review here, studies showing the effect of culture media, ovarian stimulation or embryo transfer on the methylation pattern of embryos emphasize the need to face ART-associated defects and search for strategies to mitigate adverse effects on the health of ART-derived children.

摘要

DNA 甲基化可被视为表观遗传记忆的一个组成部分,在胚胎发育过程中起着关键作用,并在受精后经历剧烈的重编程。尽管它已经成为多年来研究的焦点,但重编程机制仍未完全被理解。最近的结果表明,DNA 复制时缺乏维持是一个主要因素,并且 TET3 介导的 5mC 氧化为 5hmC 在防止从头甲基化方面起着意想不到的作用。基于分辨率和全基因组分析方法正在使更全面地评估 ART 可能损害 DNA 甲基化重编程的程度以及哪些序列元素最脆弱。事实上,正如我们在这里回顾的那样,研究显示培养基、卵巢刺激或胚胎移植对胚胎甲基化模式的影响强调了需要面对与 ART 相关的缺陷,并寻找减轻对 ART 衍生儿童健康的不利影响的策略。

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