Suppr超能文献

EED,多梳蛋白家族的一员,对于肾单位分化和肾祖细胞的维持是必需的。

EED, a member of the polycomb group, is required for nephron differentiation and the maintenance of nephron progenitor cells.

机构信息

Department of Urology, Boston Children's Hospital, Boston, MA 02115, USA.

Division of Nephrology, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Development. 2018 Jul 18;145(14):dev157149. doi: 10.1242/dev.157149.

Abstract

Epigenetic regulation of gene expression has a crucial role allowing for the self-renewal and differentiation of stem and progenitor populations during organogenesis. The mammalian kidney maintains a population of self-renewing stem cells that differentiate to give rise to thousands of nephrons, which are the functional units that carry out filtration to maintain physiological homeostasis. The polycomb repressive complex 2 (PRC2) epigenetically represses gene expression during development by placing the H3K27me3 mark on histone H3 at promoter and enhancer sites, resulting in gene silencing. To understand the role of PRC2 in nephron differentiation, we conditionally inactivated the gene, which encodes a nonredundant component of the PRC2 complex, in nephron progenitor cells. Resultant kidneys were smaller and showed premature loss of progenitor cells. The progenitors in mutant mice that were induced to differentiate did not develop into properly formed nephrons. , normally expressed in the renal vesicle, was overexpressed in kidneys of mutant mice. Thus, PRC2 has a crucial role in suppressing the expression of genes that maintain the progenitor state, allowing nephron differentiation to proceed.

摘要

基因表达的表观遗传调控在器官发生过程中对于干细胞和祖细胞群体的自我更新和分化起着至关重要的作用。哺乳动物的肾脏维持着一群自我更新的干细胞,这些干细胞分化为数千个肾单位,肾单位是执行过滤功能以维持生理内稳态的功能单位。多梳抑制复合物 2 (PRC2) 通过在启动子和增强子位点上将 H3K27me3 标记放置在组蛋白 H3 上来抑制发育过程中的基因表达,从而导致基因沉默。为了了解 PRC2 在肾单位分化中的作用,我们条件性地使编码 PRC2 复合物非冗余成分的 基因在肾祖细胞中失活。由此产生的肾脏较小,并显示出祖细胞的过早丧失。在诱导分化的 突变小鼠的祖细胞中,没有发育成适当形成的肾单位。 在 突变小鼠的肾脏中过表达,在肾小囊中正常表达。因此,PRC2 对于抑制维持祖细胞状态的基因的表达起着至关重要的作用,从而允许肾单位分化进行。

相似文献

3
Mdm2 is required for maintenance of the nephrogenic niche.Mdm2 对于肾源龛的维持是必需的。
Dev Biol. 2014 Mar 1;387(1):1-14. doi: 10.1016/j.ydbio.2014.01.009. Epub 2014 Jan 17.

引用本文的文献

3
Regulation of nephron progenitor cell lifespan and nephron endowment.调控肾祖细胞寿命和肾单位发生。
Nat Rev Nephrol. 2022 Nov;18(11):683-695. doi: 10.1038/s41581-022-00620-w. Epub 2022 Sep 14.
9
Epigenetic regulation of kidney progenitor cells.肾祖细胞的表观遗传调控
Stem Cells Transl Med. 2020 Jun;9(6):655-660. doi: 10.1002/sctm.19-0289. Epub 2020 Mar 12.
10
and -Decommissioned Fetal Enhancers are Linked to Kidney Disease.废弃的胎儿增强子与肾脏疾病有关。
J Am Soc Nephrol. 2020 Apr;31(4):765-782. doi: 10.1681/ASN.2019080797. Epub 2020 Mar 3.

本文引用的文献

1
Epigenetics of Renal Development and Disease.肾脏发育与疾病的表观遗传学
Yale J Biol Med. 2016 Dec 23;89(4):565-573. eCollection 2016 Dec.
2
Notch signaling promotes nephrogenesis by downregulating Six2.Notch信号通路通过下调Six2来促进肾发生。
Development. 2016 Nov 1;143(21):3907-3913. doi: 10.1242/dev.143503. Epub 2016 Sep 15.
3
Regulation of Genome Architecture and Function by Polycomb Proteins.多梳蛋白对基因组结构和功能的调控。
Trends Cell Biol. 2016 Jul;26(7):511-525. doi: 10.1016/j.tcb.2016.04.009. Epub 2016 May 16.
4
Development of the Mammalian Kidney.哺乳动物肾脏的发育
Curr Top Dev Biol. 2016;117:31-64. doi: 10.1016/bs.ctdb.2015.10.010. Epub 2016 Jan 23.
6
PRC2 mediated H3K27 methylations in cellular identity and cancer.PRC2介导的H3K27甲基化在细胞特性及癌症中的作用
Curr Opin Cell Biol. 2015 Dec;37:42-8. doi: 10.1016/j.ceb.2015.10.003. Epub 2015 Nov 11.
10
HTSeq--a Python framework to work with high-throughput sequencing data.HTSeq——一个用于处理高通量测序数据的Python框架。
Bioinformatics. 2015 Jan 15;31(2):166-9. doi: 10.1093/bioinformatics/btu638. Epub 2014 Sep 25.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验