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证据表明——piRNA 通路在小鼠胚胎生殖细胞中的分隔化。

Bodies of evidence - compartmentalization of the piRNA pathway in mouse fetal prospermatogonia.

机构信息

Department of Embryology, Carnegie Institution for Science, Baltimore, MD 21218, USA.

出版信息

Curr Opin Cell Biol. 2010 Dec;22(6):752-7. doi: 10.1016/j.ceb.2010.08.014. Epub 2010 Sep 6.

Abstract

Epigenetic reprogramming of embryonic mouse germ cells involves DNA demethylation of the genome that is accompanied by derepression of transposable elements (TEs). Threatening the genome's integrity, TE activation is efficiently countered by the concerted action of de novo DNA methylation and PIWI-interacting small RNAs (piRNAs). Recent studies have closely examined the subcellular localization of various piRNA pathway proteins in fetal prospermatogonia of wild-type and piRNA pathway mutant mice. Our survey highlights hierarchies and partnerships between the members of this ancient defensive mechanism. Overall, the elaborate cytoplasmic compartmentalization of the piRNA pathway in fetal prospermatogonia provides a highly informative context to aid our understanding of the mouse piRNA pathway.

摘要

胚胎期小鼠生殖细胞的表观遗传重编程涉及基因组的 DNA 去甲基化,伴随着转座元件(TEs)的去抑制。TE 的激活威胁着基因组的完整性,而新合成的 DNA 甲基化和 PIWI 相互作用的小 RNA(piRNAs)的协同作用有效地阻止了这一过程。最近的研究密切观察了各种 piRNA 途径蛋白在野生型和 piRNA 途径突变体小鼠的胎儿原生殖细胞中的亚细胞定位。我们的调查突出了这个古老防御机制成员之间的层次结构和伙伴关系。总的来说,piRNA 途径在胎儿原生殖细胞中的精细细胞质区室化提供了一个非常有信息量的背景,有助于我们理解小鼠 piRNA 途径。

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