首页> 外文期刊>The Journal of biological chemistry >Involvement of 14-3-3 Proteins in the Second Epidermal Growth Factor-induced Wave of Rac1 Activation in the Process of Cell Migration
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Involvement of 14-3-3 Proteins in the Second Epidermal Growth Factor-induced Wave of Rac1 Activation in the Process of Cell Migration

机译:在细胞迁移过程中,14-3-3蛋白在第二表皮生长因子诱导的RAC1激活波中的参与

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Immense previous efforts have elucidated the core machinery in cell migration, actin remodeling regulated by Rho family small GTPases including RhoA, Cdc42, and Rac1; however, the spatiotemporal regulation of these molecules remains largely unknown. Here, we report that EGF induces biphasic Rac1 activation in the process of cell migration, and UTKO1, a cell migration inhibitor, inhibits the second EGF-induced wave of Rac1 activation but not the first wave. To address the regulation mechanism and role of the second wave of Rac1 activation, we identified 14-3-3ζ as a target protein of UTKO1 and also showed that UTKO1 abrogated the binding of 14-3-3ζ to Tiam1 that was responsible for the second wave of Rac1 activation, suggesting that the interaction of 14-3-3ζ with Tiam1 is involved in this event. To our knowledge, this is the first report to use a chemical genetic approach to demonstrate the mechanism of temporal activation of Rac1.
机译:巨大的以前的努力阐明了细胞迁移中的核心机械,由rho家族小GTP酶调节的肌动蛋白重塑,包括RhoA,CDC42和RAC1;然而,这些分子的时空调节仍然很大程度上是未知的。这里,我们报告说,EGF在细胞迁移过程中引起双相环RAC1激活,并且UTKO1,细胞迁移抑制剂抑制RAC1激活的第二EGF感应波,但不是第一波。为了解决第二波RAC1激活的调节机制和作用,我们鉴定了14-3-3- utko1的靶蛋白,并且还显示UTKO1废除了14-3-3-3-3-3-的结合,这是对第二次负责的TIAM1 RAC1激活浪潮,表明,在此事件中涉及14-3-3ζ的相互作用。为了我们的知识,这是第一份使用化学遗传方法来证明RAC1的时间激活机制的报告。

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