Kibra Is a Regulator of the Salvador/Warts/Hippo Signaling Network

被引:333
作者
Genevet, Alice [2 ]
Wehr, Michael C. [2 ]
Brain, Ruth [1 ]
Thompson, Barry J. [1 ]
Tapon, Nicolas [2 ]
机构
[1] Canc Res UK, London Res Inst, Epithelial Biol Lab, London WC2A 3PX, England
[2] Canc Res UK, London Res Inst, Apoptosis & Proliferat Control Lab, London WC2A 3PX, England
关键词
PROTEIN-PROTEIN INTERACTIONS; WARTS-HIPPO PATHWAY; CELL-PROLIFERATION; AXIS SPECIFICATION; DROSOPHILA; GROWTH; APOPTOSIS; PROMOTES; HOMOLOG; GENES;
D O I
10.1016/j.devcel.2009.12.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Salvador (Sav)/Warts (Wts)/Hippo (Hpo) (SWH) network controls tissue growth by inhibiting cell proliferation and promoting apoptosis. The core of the pathway consists of a MST and LATS family kinase cascade that ultimately phosphorylates and inactivates the YAP/Yorkie (Yki) transcription coactivator. The FERM domain proteins Merlin (Mer) and Expanded (Ex) represent one mode of upstream regulation controlling pathway activity. Here, we identify Kibra as a member of the SWH network. Kibra, which colocalizes and associates with Mer and Ex, also promotes the Mer/Ex association. Furthermore, the Kibra/Mer association is conserved in human cells. Finally, Kibra complexes with Wts and kibra depletion in tissue culture cells induces a marked reduction in Yki phosphorylation without affecting the Yki/Wts interaction. We suggest that Kibra is part of an apical scaffold that promotes SWH pathway activity.
引用
收藏
页码:300 / 308
页数:9
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