The role of YAP transcription coactivator in regulating stem cell self-renewal and differentiation

被引:627
作者
Lian, Ian [1 ]
Kim, Joungmok [1 ]
Okazawa, Hideki [1 ]
Zhao, Jiagang [1 ]
Zhao, Bin [1 ]
Yu, Jindan [2 ]
Chinnaiyan, Arul [3 ]
Israel, Mason A. [4 ]
Goldstein, Lawrence S. B. [4 ]
Abujarour, Ramzey [5 ]
Ding, Sheng [5 ]
Guan, Kun-Liang [1 ,6 ]
机构
[1] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
[2] Northwestern Univ, Feinberg Med Sch, Robert H Lurie Canc Ctr, Div Hematol Oncol, Chicago, IL 60611 USA
[3] Univ Michigan, Sch Med, Michigan Ctr Translat Pathol, Ann Arbor, MI 48109 USA
[4] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[5] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[6] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
关键词
YAP; Hippo; stem cells; TEAD; YES-ASSOCIATED PROTEIN; WW DOMAIN; TEAD/TEF FAMILY; ORGAN SIZE; PATHWAY; DROSOPHILA; INDUCTION; TEAD4; GENE; LATS;
D O I
10.1101/gad.1903310
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Yes-associated protein (YAP) is a potent transcription coactivator acting via binding to the TEAD transcription factor, and plays a critical role in organ size regulation. YAP is phosphorylated and inhibited by the Lats kinase, a key component of the Hippo tumor suppressor pathway. Elevated YAP protein levels and gene amplification have been implicated in human cancer. In this study, we report that YAP is inactivated during embryonic stem (ES) cell differentiation, as indicated by decreased protein levels and increased phosphorylation. Consistently, YAP is elevated during induced pluripotent stem (iPS) cell reprogramming. YAP knockdown leads to a loss of ES cell pluripotency, while ectopic expression of YAP prevents ES cell differentiation in vitro and maintains stem cell phenotypes even under differentiation conditions. Moreover, YAP binds directly to promoters of a large number of genes known to be important for stem cells and stimulates their expression. Our observations establish a critical role of YAP in maintaining stem cell pluripotency.
引用
收藏
页码:1106 / 1118
页数:13
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