TGF-β control of stem cell differentiation genes

被引:149
作者
Massague, Joan [1 ,2 ]
Xi, Qiaoran [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Canc Biol & Genet Program, New York, NY 10021 USA
[2] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
关键词
Stem cell; Chromatin; Epigenetic; Transcription; Differentiation; TGF-beta; GROWTH-FACTOR-BETA; UBIQUITIN LIGASE; VERTEBRATE DEVELOPMENT; EMBRYONIC-DEVELOPMENT; HISTONE MODIFICATIONS; TRANSCRIPTION FACTORS; BINDING PROTEIN; NUCLEAR IMPORT; SMAD PATHWAY; CHROMATIN;
D O I
10.1016/j.febslet.2012.03.023
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
The canonical TGF-beta/Smad signaling pathway was delineated in the mid 90s and enriched over the past decade with many findings about its specificity, regulation, networking, and malfunctions in disease. However, a growing understanding of the chromatin status of a critical class of TGF-beta target genes - the genes controlling differentiation of embryonic stem cells - recently prompted a reexamination of this pathway and its critical role in the regulation of stem cell differentiation. The new findings reveal master regulators of the pluripotent state set the stage for Smad-mediated activation of master regulators of the next differentiation stage. Furthermore, a novel branch of the TGF-beta/Smad pathway has been identified in which a chromatin-reading Smad complex makes the master differentiation genes accessible to canonical Smad complexes for transcriptional activation. These findings provide exciting new insights into the global role of TGF-beta signaling in the regulators of stem cell fate. (C) 2012 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1953 / 1958
页数:6
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