Integrating post-transcriptional regulation into the embryonic stem cell gene regulatory network

被引:10
作者
Cassar, Paul A. [1 ]
Stanford, William L. [1 ,2 ,3 ,4 ]
机构
[1] Univ Toronto, Inst Med Sci, Toronto, ON M5S 3G9, Canada
[2] Univ Toronto, Inst Biomat & Biomed Engn, Toronto, ON M5S 3G9, Canada
[3] Inst Syst Biol, Seattle, WA USA
[4] Ottawa Hosp, Res Inst, Sprott Ctr Stem Cell Res, Ottawa, ON, Canada
关键词
RNA-BINDING PROTEIN; NOVO DNA METHYLATION; SELF-RENEWAL; MESSENGER-RNA; GENOME-WIDE; TARGETED DISRUPTION; RIBONUCLEOPROTEIN COMPLEXES; TRANSCRIPTIONAL NETWORKS; DEVELOPMENTAL REGULATORS; SIGNALING PATHWAYS;
D O I
10.1002/jcp.22787
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Stem cell behavior is orchestrated as a multilayered, concert of gene regulatory mechanisms collectively referred to as the gene regulatory network (GRN). Via cooperative mechanisms, transcriptional, epigenetic, and post-transcriptional regulators activate and repress gene expression to finely regulate stem cell self-renewal and commitment. Due to their tractability, embryonic stem cells (ESCs) serve as the model stem cell to dissect the complexities of the GRN, and discern its relation to stem cell fate. By way of high-throughput genomic analysis, targets of individual gene regulators have been established in ESCs. The compilation of these discrete networks has revealed convergent, multi-dimensional gene regulatory mechanisms involving transcription factors, epigenetic modifiers, non-coding RNA (ncRNA), and RNA-binding proteins. Here we highlight the seminal genomic studies that have shaped our understanding of the ESC GRN and describe alternate post-transcriptional gene regulatory mechanisms that require in depth analyses to draft networks that fully model ESC behavior. J. Cell. Physiol. 227: 439449, 2012. (C) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:439 / 449
页数:11
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