Wnt信号通路
生物
细胞生物学
WNT3A型
连环蛋白
转录因子
LRP6型
LRP5
信号转导
效应器
遗传学
基因
作者
Hyun Woo Park,Young Chul Kim,Bo Yu,Toshiro Moroishi,Jung-Soon Mo,Steven W. Plouffe,Zhipeng Meng,Kimberly C. Lin,Fa‐Xing Yu,Caroline M. Alexander,Cun-Yu Wang,Kun‐Liang Guan
出处
期刊:Cell
[Elsevier]
日期:2015-08-01
卷期号:162 (4): 780-794
被引量:574
标识
DOI:10.1016/j.cell.2015.07.013
摘要
The transcriptional co-activators YAP and TAZ are key regulators of organ size and tissue homeostasis, and their dysregulation contributes to human cancer. Here, we discover YAP/TAZ as bona fide downstream effectors of the alternative Wnt signaling pathway. Wnt5a/b and Wnt3a induce YAP/TAZ activation independent of canonical Wnt/β-catenin signaling. Mechanistically, we delineate the “alternative Wnt-YAP/TAZ signaling axis” that consists of Wnt-FZD/ROR-Gα12/13-Rho GTPases-Lats1/2 to promote YAP/TAZ activation and TEAD-mediated transcription. YAP/TAZ mediate the biological functions of alternative Wnt signaling, including gene expression, osteogenic differentiation, cell migration, and antagonism of Wnt/β-catenin signaling. Together, our work establishes YAP/TAZ as critical mediators of alternative Wnt signaling.
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