Structural dissection of Hippo signaling

被引:12
作者
Shi, Zhubing [1 ,2 ]
Jiao, Shi [1 ]
Zhou, Zhaocai [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Natl Ctr Prot Sci Shanghai, State Key Lab Cell Biol,Inst Biochem & Cell Biol, Shanghai 200031, Peoples R China
[2] Tongji Univ, Sch Life Sci & Technol, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
Hippo pathway; three-dimensional structure; protein-protein; DNA interaction; regulatory mechanism; ORGAN SIZE CONTROL; PROTEIN-INTERACTION NETWORK; TEAD TRANSCRIPTION FACTORS; TUMOR-SUPPRESSOR LATS1; CELL SELF-RENEWAL; WW DOMAIN; PROMOTES APOPTOSIS; CRYSTAL-STRUCTURE; DROSOPHILA-MELANOGASTER; PROLIFERATION ARREST;
D O I
10.1093/abbs/gmu107
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
The Hippo pathway controls cell number and organ size by restricting cell proliferation and promoting apoptosis, and thus is a key regulator in development and homeostasis. Dysfunction of the Hippo pathway correlates with many pathological conditions, especially cancer. Hippo signaling also plays important roles in tissue regeneration and stem cell biology. Therefore, the Hippo pathway is recognized as a crucial target for cancer therapy and regeneration medicine. To date, structures of several key components in Hippo signaling have been determined. In this review, we summarize current available structural studies of the Hippo pathway, which may help to improve our understanding of its regulatory mechanisms, as well as to facilitate further functional studies and potential therapeutic interventions.
引用
收藏
页码:29 / 38
页数:10
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