Ubiquitination of Tumor Necrosis Factor Receptor-associated Factor 4 (TRAF4) by Smad Ubiquitination Regulatory Factor 1 (Smurf1) Regulates Motility of Breast Epithelial and Cancer Cells

被引:45
作者
Wang, Xiangchun [1 ]
Jin, Chaoyang [1 ]
Tang, Yi [1 ]
Tang, Liu-Ya [1 ]
Zhang, Ying E. [1 ]
机构
[1] NCI, Lab Cellular & Mol Biol, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
Breast Cancer; Cell Migration; E3 Ubiquitin Ligase; Rac1; Tight Junctions; TRAF; Ubiquitination; Smurf1; TRAF4; Monoubiquitination; LIGASE SMURF2; TRAF4-DEFICIENT MICE; TGF-BETA; DEGRADATION; POLARITY; PATHWAY; MIGRATION; TARGETS; PROTEIN; DIFFERENTIATION;
D O I
10.1074/jbc.M113.472704
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
Smad ubiquitin regulatory factors (Smurfs) are HECT-domain ubiquitin E3 ligases that regulate diverse cellular processes, including normal and tumor cell migration. However, the underlying mechanism of the Smurfs' role in cell migration is not fully understood. Here we show that Smurf1 induces ubiquitination of tumor necrosis factor receptor-associated factor 4 (TRAF4) at K190. Using the K190R mutant of TRAF4, we demonstrate that Smurf1-induced ubiquitination is required for proper localization of TRAF4 to tight junctions in confluent epithelial cells. We further show that TRAF4 is essential for the migration of both normal mammary epithelial and breast cancer cells. The ability of TRAF4 to promote cell migration is also dependent on Smurf1-mediated ubiquitination, which is associated with Rac1 activation by TRAF4. These results reveal a new regulatory circuit for cell migration, consisting of Smurf1-mediated ubiquitination of TRAF4 and Rac1 activation.
引用
收藏
页码:21784 / 21792
页数:9
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