首页> 外文期刊>The Journal of biological chemistry >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
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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

机译:肿瘤坏死因子受体相关因子4(TRAF4)通过SMAD泛素调节因子1(SMURF1)调节乳腺上皮和癌细胞的运动

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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.
机译:SMAD泛素调节因子(SMURF)是杂交域泛素E3连接酶,其调节不同的细胞过程,包括正常和肿瘤细胞迁移。然而,水肿在细胞迁移中的角色的潜在机制尚不完全理解。在这里,我们表明SMURF1在K190处诱导肿瘤坏死因子受体相关因子4(TRAF4)的泛素。使用Traf4的K190R突变体,我们证明了SMURF1诱导的泛素化是为了将TRAF4的适当定位到汇合上皮细胞中的紧密交叉点。我们进一步表明,TRAF4对于常规乳腺上皮和乳腺癌细胞的迁移至关重要。 TRAF4促进细胞迁移的能力也依赖于SMURF1介导的泛素,其与TRAF4的RAC1激活相关。这些结果揭示了细胞迁移的新调节赛,由Smurf1介导的Traf4和Rac1活化的泛素化。

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