Structural Insights into the Regulation of Hippo Signaling

被引:18
作者
Cairns, Leah [1 ]
Thao Tran [1 ]
Kavran, Jennifer M. [1 ,2 ]
机构
[1] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Biochem & Mol Biol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Biophys & Biophys Chem, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
HYDROPHOBIC MOTIF PHOSPHORYLATION; NDR-PROTEIN-KINASE; ORGAN SIZE CONTROL; CELL-CYCLE EXIT; TUMOR-SUPPRESSOR; FERM-DOMAIN; WW DOMAIN; NEUROFIBROMATOSIS TYPE-2; PROMOTES APOPTOSIS; CRYSTAL-STRUCTURE;
D O I
10.1021/acschembio.6b01058
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
During development, the Hippo pathway regulates the balance between cell proliferation and apoptosis to control organ size. Appropriate Hippo signaling is associated with stem cell maintenance, while inappropriate signaling can result in tumorigenesis and cancer. Cellular and genetic investigations have identified core components and determined that complex formation and protein phosphorylation are crucial regulatory events. The recent spate of high-resolution structures of Hippo pathway components have begun to reveal the molecular mechanisms controlling these events, including the molecular determinates of complex formation between YAP and TEAD, the role of phosphorylation in controlling complex formation by Mob, and the conformational changes accompanying Mst1/2 kinase domain activation. We will review these advances and revisit previous structures to provide a comprehensive overview of the structural changes associated with the regulation of this pathway as well as discuss areas that could benefit from further mechanistic studies.
引用
收藏
页码:601 / 610
页数:10
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