Amot130 Adapts Atrophin-1 Interacting Protein 4 to Inhibit Yes-associated Protein Signaling and Cell Growth

被引:55
作者
Adler, Jacob J. [1 ]
Heller, Brigitte L. [1 ]
Bringman, Lauren R. [1 ]
Ranahan, William P. [1 ]
Cocklin, Ross R. [1 ]
Goebl, Mark G. [1 ]
Oh, Misook [1 ]
Lim, Hyun-Suk [1 ]
Ingham, Robert J. [2 ]
Wells, Clark D. [1 ]
机构
[1] Indiana Univ Sch Med, Dept Biochem & Mol Biol, Indianapolis, IN 46202 USA
[2] Univ Alberta, Dept Med Microbiol & Immunol, Li Ka Shing Inst Virol, Edmonton, AB T6G 2E1, Canada
基金
美国国家卫生研究院;
关键词
E3 UBIQUITIN LIGASE; TUMOR-SUPPRESSOR; WW DOMAINS; NEGATIVE REGULATOR; HIPPO PATHWAY; COILED-COIL; ANGIOMOTIN; ITCH; YAP; COMPLEX;
D O I
10.1074/jbc.M112.446534
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 adaptor protein Amot130 scaffolds components of the Hippo pathway to promote the inhibition of cell growth. This study describes how Amot130 through binding and activating the ubiquitin ligase AIP4/Itch achieves these effects. AIP4 is found to bind and ubiquitinate Amot130 at residue Lys-481. This both stabilizes Amot130 and promotes its residence at the plasma membrane. Furthermore, Amot130 is shown to scaffold a complex containing overexpressed AIP4 and the transcriptional co-activator Yes-associated protein (YAP). Consequently, Amot130 promotes the ubiquitination of YAP by AIP4 and prevents AIP4 from binding to large tumor suppressor 1. Amot130 is found to reduce YAP stability. Importantly, Amot130 inhibition of YAP dependent transcription is reversed by AIP4 silencing, whereas Amot130 and AIP4 expression interdependently suppress cell growth. Thus, Amot130 repurposes AIP4 from its previously described role in degrading large tumor suppressor 1 to the inhibition of YAP and cell growth.
引用
收藏
页码:15181 / 15193
页数:13
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