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小鼠滋养层干细胞中的转录调控

Transcriptional regulation of in mouse trophoblast stem cells.

作者信息

Yu Wei, Chakravarthi V Praveen, Borosha Shaon, Dilower Iman, Lee Eun Bee, Ratri Anamika, Starks Rebekah R, Fields Patrick E, Wolfe Michael W, Faruque M Omar, Tuteja Geetu, Rumi M A Karim

机构信息

Department of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, KS, United States.

Department of Genetics, Development and Cell Biology, Iowa State University, Ames, IA, United States.

出版信息

Front Cell Dev Biol. 2022 Dec 14;10:918235. doi: 10.3389/fcell.2022.918235. eCollection 2022.

Abstract

SATB homeobox proteins are important regulators of developmental gene expression. Among the stem cell lineages that emerge during early embryonic development, trophoblast stem (TS) cells exhibit robust SATB expression. Both SATB1 and SATB2 act to maintain the trophoblast stem-state. However, the molecular mechanisms that regulate TS-specific expression are not yet known. We identified Satb1 variant 2 as the predominant transcript in trophoblasts. Histone marks, and RNA polymerase II occupancy in TS cells indicated an active state of the promoter. A novel cis-regulatory region with active histone marks was identified ∼21 kbp upstream of the variant 2 promoter. CRISPR/Cas9 mediated disruption of this sequence decreased Satb1 expression in TS cells and chromosome conformation capture analysis confirmed looping of this distant regulatory region into the proximal promoter. Scanning position weight matrices across the enhancer predicted two ELF5 binding sites in close proximity to SATB1 sites, which were confirmed by chromatin immunoprecipitation. Knockdown of ELF5 downregulated Satb1 expression in TS cells and overexpression of ELF5 increased the enhancer-reporter activity. Interestingly, ELF5 interacts with SATB1 in TS cells, and the enhancer activity was upregulated following SATB overexpression. Our findings indicate that trophoblast-specific Satb1 expression is regulated by long-range chromatin looping of an enhancer that interacts with ELF5 and SATB proteins.

摘要

SATB同源框蛋白是发育基因表达的重要调节因子。在早期胚胎发育过程中出现的干细胞谱系中,滋养层干细胞(TS)表现出强烈的SATB表达。SATB1和SATB2都起到维持滋养层干细胞状态的作用。然而,调节TS特异性表达的分子机制尚不清楚。我们鉴定出Satb1变体2是滋养层细胞中的主要转录本。组蛋白标记以及TS细胞中的RNA聚合酶II占有率表明启动子处于活跃状态。在变体2启动子上游约21kbp处鉴定出一个具有活跃组蛋白标记的新型顺式调节区域。CRISPR/Cas9介导的该序列破坏降低了TS细胞中Satb1的表达,并且染色体构象捕获分析证实了这个远距离调节区域与近端启动子形成环化。对增强子进行扫描位置权重矩阵分析预测出两个紧邻SATB1位点的ELF5结合位点,这通过染色质免疫沉淀得到证实。敲低ELF5可下调TS细胞中Satb1的表达,而ELF5的过表达则增加增强子报告基因活性。有趣的是,ELF5在TS细胞中与SATB1相互作用,并且在SATB过表达后增强子活性上调。我们的研究结果表明,滋养层特异性Satb1表达受与ELF5和SATB蛋白相互作用的增强子的长程染色质环化调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a8/9795202/1cfe16d4e6b1/fcell-10-918235-g001.jpg

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