A ZO-2 scaffolding mechanism regulates the Hippo signalling pathway.

Olivia Xuan Liu, Lester Bocheng Lin, Soumya Bunk, Tiweng Chew, Selwin K Wu, Fumio Motegi, Boon Chuan Low
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引用次数: 0

Abstract

Contact inhibition of proliferation is a critical cell density control mechanism governed by the Hippo signalling pathway. The biochemical signalling underlying cell density-dependent cues regulating Hippo signalling and its downstream effectors, YAP, remains poorly understood. Here, we reveal that the tight junction protein ZO-2 is required for the contact-mediated inhibition of proliferation. We additionally determined that the well-established molecular players of this process, namely Hippo kinase LATS1 and YAP, are regulated by ZO-2 and that the scaffolding function of ZO-2 promotes the interaction with and phosphorylation of YAP by LATS1. Mechanistically, YAP is phosphorylated when ZO-2 brings LATS1 and YAP together via its SH3 and PDZ domains, respectively, subsequently leading to the cytoplasmic retention and inactivation of YAP. In conclusion, we demonstrate that ZO-2 maintains Hippo signalling pathway activation by promoting the stability of LATS1 to inactivate YAP.

ZO-2支架机制调节Hippo信号通路。
增殖的接触抑制是一种关键的细胞密度控制机制,由 Hippo 信号通路控制。细胞密度依赖性线索调控 Hippo 信号及其下游效应物 YAP 的生化信号仍然鲜为人知。在这里,我们发现紧密连接蛋白 ZO-2 是接触介导的增殖抑制所必需的。此外,我们还确定了这一过程中公认的分子角色(即 Hippo 激酶 LATS1 和 YAP)受 ZO-2 调节,并且 ZO-2 的支架功能促进了 LATS1 与 YAP 的相互作用和 YAP 的磷酸化。从机理上讲,当 ZO-2 分别通过其 SH3 和 PDZ 结构域将 LATS1 和 YAP 结合在一起时,YAP 就会被磷酸化,随后导致 YAP 在细胞质中滞留和失活。总之,我们证明了ZO-2通过促进LATS1的稳定性使YAP失活来维持Hippo信号通路的激活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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