Division of Molecular Genetics, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Division of Molecular Carcinogenesis, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Gastroenterology. 2016 Oct;151(4):684-697.e12. doi: 10.1053/j.gastro.2016.06.020. Epub 2016 Jun 21.
BACKGROUND & AIMS: The polycomb repressive complex 2 (PRC2) regulates differentiation by contributing to repression of gene expression and thereby stabilizing the fate of stem cells and their progeny. PRC2 helps to maintain adult stem cell populations, but little is known about its functions in intestinal stem cells. We studied phenotypes of mice with intestine-specific deletion of the PRC2 proteins embryonic ectoderm development (EED) (a subunit required for PRC2 function) and enhancer of zeste homolog 2 (EZH2) (a histone methyltransferase).
We performed studies of AhCre;EedLoxP/LoxP (EED knockout) mice and AhCre;Ezh2LoxP/LoxP (EZH2 knockout) mice, which have intestine-specific disruption in EED and EZH2, respectively. Small intestinal crypts were isolated and subsequently cultured to grow organoids. Intestines and organoids were analyzed by immunohistochemical, in situ hybridization, RNA sequence, and chromatin immunoprecipitation methods.
Intestines of EED knockout mice had massive crypt degeneration and lower numbers of proliferating cells compared with wild-type control mice. Cdkn2a became derepressed and we detected increased levels of P21. We did not observe any differences between EZH2 knockout and control mice. Intestinal crypts from EED knockout mice had signs of aberrant differentiation of uncommitted crypt cells-these differentiated toward the secretory cell lineage. Furthermore, crypts from EED-knockout mice had impaired Wnt signaling and concomitant loss of intestinal stem cells, this phenotype was not reversed upon ectopic stimulation of Wnt and Notch signaling in organoids. Analysis of gene expression patterns from intestinal tissues of EED knockout mice showed dysregulation of several genes involved in Wnt signaling. Wnt signaling was regulated directly by PRC2.
In intestinal tissues of mice, PRC2 maintains small intestinal stem cells by promoting proliferation and preventing differentiation in the intestinal stem cell compartment. PRC2 controls gene expression in multiple signaling pathways that regulate intestinal homeostasis. Sequencing data are available in the genomics data repository GEO under reference series GSE81578; RNA sequencing data are available under subseries GSE81576; and ChIP sequencing data are available under subseries GSE81577.
多梳抑制复合物 2(PRC2)通过促进基因表达的抑制来调节分化,从而稳定干细胞及其后代的命运。PRC2 有助于维持成体干细胞群体,但对于其在肠道干细胞中的功能知之甚少。我们研究了肠道特异性缺失 PRC2 蛋白胚胎外胚层发育(EED)(PRC2 功能所必需的一个亚基)和增强子的 zeste 同源物 2(EZH2)(一种组蛋白甲基转移酶)的小鼠表型。
我们对 AhCre;EedLoxP/LoxP(EED 敲除)小鼠和 AhCre;Ezh2LoxP/LoxP(EZH2 敲除)小鼠进行了研究,这两种小鼠分别在肠道特异性缺失 EED 和 EZH2。从小肠隐窝中分离出并随后培养以生长类器官。通过免疫组织化学、原位杂交、RNA 测序和染色质免疫沉淀方法分析肠道和类器官。
与野生型对照小鼠相比,EED 敲除小鼠的小肠隐窝大量退化,增殖细胞数量减少。Cdkn2a 被去抑制,我们检测到 P21 水平升高。我们没有观察到 EZH2 敲除与对照小鼠之间的任何差异。EED 敲除小鼠的肠隐窝显示未分化隐窝细胞的异常分化迹象-这些细胞向分泌细胞谱系分化。此外,EED 敲除小鼠的隐窝中 Wnt 信号受损,同时伴有肠干细胞丧失,这种表型在类器官中异位刺激 Wnt 和 Notch 信号时并未逆转。对 EED 敲除小鼠肠道组织的基因表达模式分析显示,几个参与 Wnt 信号的基因发生了失调。Wnt 信号直接受 PRC2 调节。
在小鼠的肠道组织中,PRC2 通过促进增殖和防止肠干细胞区室中的分化来维持小肠干细胞。PRC2 控制调节肠道稳态的多个信号通路中的基因表达。测序数据可在基因组学数据存储库 GEO 中参考系列 GSE81578 中获得;RNA 测序数据可在子系列 GSE81576 中获得;ChIP 测序数据可在子系列 GSE81577 中获得。