| Literature DB >> 30472188 |
Zhengkui Zhang1, Jinjin Du2, Shuai Wang3, Li Shao4, Ke Jin2, Fang Li2, Bajin Wei5, Wei Ding5, Peifen Fu5, Hans van Dam6, Aijun Wang7, Jin Jin2, Chen Ding8, Bing Yang2, Min Zheng4, Xin-Hua Feng2, Kun-Liang Guan9, Long Zhang10.
Abstract
The transcriptional regulators YAP and TAZ play important roles in development, physiology, and tumorigenesis and are negatively controlled by the Hippo pathway. It is yet unknown why the YAP/ TAZ proteins are frequently activated in human malignancies in which the Hippo pathway is still active. Here, by a gain-of-function cancer metastasis screen, we discovered OTUB2 as a cancer stemness and metastasis-promoting factor that deubiquitinates and activates YAP/TAZ. We found OTUB2 to be poly-SUMOylated on lysine 233, and this SUMOylation enables it to bind YAP/TAZ. We also identified a yet-unknown SUMO-interacting motif (SIM) in YAP and TAZ required for their association with SUMOylated OTUB2. Importantly, EGF and oncogenic KRAS induce OTUB2 poly-SUMOylation and thereby activate YAP/TAZ. Our results establish OTUB2 as an essential modulator of YAP/TAZ and also reveal a novel mechanism via which YAP/TAZ activity is induced by oncogenic KRAS.Entities:
Keywords: OTUB2; SUMOylation; YAP/TAZ; deubiquitination; metastasis
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Year: 2018 PMID: 30472188 DOI: 10.1016/j.molcel.2018.10.030
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970