The Hippo signaling pathway coordinately regulates cell proliferation and apoptosis by inactivating Yorkie, the Drosophila homolog of YAP

被引:1501
作者
Huang, JB [1 ]
Wu, S [1 ]
Barrera, J [1 ]
Matthews, K [1 ]
Pan, DJ [1 ]
机构
[1] Univ Texas, SW Med Ctr, Dept Physiol, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.cell.2005.06.007
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
Coordination between cell proliferation and cell death is essential to maintain homeostasis in multicellular organisms. In Drosophila, these two processes are regulated by a pathway involving the Ste20-like kinase Hippo (Hpo) and the NDR family kinase Warts (Wts; also called Lats). Hpo phosphorylates and activates Wts, which in turn, through unknown mechanisms, negatively regulates the transcription of cell-cycle and cell-death regulators such as cycE and diap1. Here we identify Yorkie (Yki), the Drosophila ortholog of the mammalian transcriptional coactivator yes-associated protein (YAP), as a missing link between Wts and transcriptional regulation. Yki is required for normal tissue growth and diapl transcription and is phosphorylated and inactivated by Wts. Overexpression of yki phenocopies loss-of-function mutations of hpo or wts, including elevated transcription of cycE and diapl, increased proliferation, defective apoptosis, and tissue overgrowth. Thus, Yki Is a critical target of the Wts/Lats protein kinase and a potential oncogene.
引用
收藏
页码:421 / 434
页数:14
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