Nanog Expression in Embryonic Stem Cells - An Ideal Model System to Dissect Enhancer Function

被引:19
作者
Blinka, Steven [1 ,2 ]
Rao, Sridhar [1 ,2 ,3 ]
机构
[1] Med Coll Wisconsin, Dept Cell Biol Neurobiol & Anat, Milwaukee, WI 53226 USA
[2] Blood Ctr Wisconsin, Blood Res Inst, 8733 West Watertown Plank Rd, Milwaukee, WI 53226 USA
[3] Med Coll Wisconsin, Dept Pediat, 8701 Watertown Plank Rd, Milwaukee, WI 53226 USA
关键词
embryonic stem cells; eRNAs; higher order chromosome structure; looping; transcriptional regulation; super-enhancers; SUPER-ENHANCERS; GROUND-STATE; TRANSCRIPTIONAL NETWORK; GENE-EXPRESSION; INSULATED NEIGHBORHOODS; CHROMATIN ARCHITECTURE; REGULATORY CIRCUITRY; PLURIPOTENCY FACTORS; TOPOLOGICAL DOMAINS; SIGNALING PATHWAYS;
D O I
10.1002/bies.201700086
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Embryonic stem cells (ESCs) are derived from the preimplantation embryo and can differentiate into virtually any other cell type (termed pluripotency), which is governed by lineage specific transcriptions factors (TFs) binding to cis regulatory elements (CREs) to mediate changes in gene expression. The reliance on transcriptional regulation to maintain pluripotency makes ESCs a valuable model to study the role of distal CREs such as enhancers in modulating gene expression to affect cell fate decisions. This review will highlight recent advance on transcriptional enhancers, focusing on studies performed in ESCs. In addition, we argue that the Nanog locus, which encodes for an ESC-critical TF, is particularly informative because it contains multiple co-regulated genes and enhancers in close proximity to one another. The unique landscape at Nanog permits the study of ongoing questions including whether multiple enhancers function additively versus synergistically, determinants of gene specificity, and cell-to-cell variability in gene expression. See also the video abstract here: https://youtu.be/tnW2Z6bYF8E.
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页数:11
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