Cairns Leah, Tran Thao, Kavran Jennifer M
Department of Biochemistry and Molecular Biology, Bloomberg School of Public Health and ‡Department of Biophysics and Biophysical Chemistry, School of Medicine, Johns Hopkins University , Baltimore, Maryland 21205, United States.
ACS Chem Biol. 2017 Mar 17;12(3):601-610. doi: 10.1021/acschembio.6b01058. Epub 2017 Feb 9.
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.
在发育过程中,河马通路调节细胞增殖和凋亡之间的平衡以控制器官大小。适当的河马信号传导与干细胞维持相关,而不适当的信号传导可导致肿瘤发生和癌症。细胞和遗传学研究已经确定了核心成分,并确定复合物形成和蛋白质磷酸化是关键的调节事件。最近一系列河马通路成分的高分辨率结构已开始揭示控制这些事件的分子机制,包括YAP和TEAD之间复合物形成的分子决定因素、磷酸化在通过Mob控制复合物形成中的作用以及伴随Mst1/2激酶结构域激活的构象变化。我们将回顾这些进展并重新审视以前的结构,以全面概述与该通路调节相关的结构变化,并讨论可能从进一步的机制研究中受益的领域。