The transcriptional regulation of pluripotency

被引:97
|
作者
Yeo, Jia-Chi [1 ,2 ]
Ng, Huck-Hui [1 ,2 ,3 ,4 ,5 ]
机构
[1] Genome Inst Singapore, Gene Regulat Lab, Singapore 138672, Singapore
[2] Nanyang Technol Univ, Sch Biol Sci, Singapore 637551, Singapore
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Singapore 117597, Singapore
[4] Natl Univ Singapore, Dept Biol Sci, Singapore 117543, Singapore
[5] Natl Univ Singapore, NUS Grad Sch Integrat Sci & Engn, Singapore 117456, Singapore
关键词
embryonic stem cells; pluripotency; ESCs; EpiSCs; transcriptional regulation; gene expression; signaling pathways; naive; primed; EMBRYONIC STEM-CELLS; PROTEIN-INTERACTION NETWORK; SELF-RENEWAL; MOUSE EPIBLAST; GROUND-STATE; RNAI SCREEN; C-MYC; HOMOLOGOUS RECOMBINATION; SIGNALING PATHWAYS; GENE-EXPRESSION;
D O I
10.1038/cr.2012.172
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The defining features of embryonic stem cells (ESCs) are their self-renewing and pluripotent capacities. Indeed, the ability to give rise into all cell types within the organism not only allows ESCs to function as an ideal in vitro tool to study embryonic development, but also offers great therapeutic potential within the field of regenerative medicine. However, it is also this same remarkable developmental plasticity that makes the efficient control of ESC differentiation into the desired cell type very difficult. Therefore, in order to harness ESCs for clinical applications, a detailed understanding of the molecular and cellular mechanisms controlling ESC pluripotency and lineage commitment is necessary. In this respect, through a variety of transcriptomic approaches, ESC pluripotency has been found to be regulated by a system of ESC-associated transcription factors; and the external signalling environment also acts as a key factor in modulating the ESC transcriptome. Here in this review, we summarize our current understanding of the transcriptional regulatory network in ESCs, discuss how the control of various signalling pathways could influence pluripotency, and provide a future outlook of ESC research.
引用
收藏
页码:20 / 32
页数:13
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