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Interaction of RhoD and ZIP kinase modulates actin filament assembly and focal adhesion dynamics

机译:RhoD和ZIP激酶的相互作用调节肌动蛋白丝装配和粘着动力学

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RhoD is a member of the classical Rho GTPases and it has an essential role in the regulation of actin dynamics. Furthermore, RhoD also localizes to early endosomes and recycling endosomes, indicating additional roles in the regulation of endosome trafficking. A yeast two-hybrid screen identified Zipper-Interacting Protein Kinase (ZIPK) as a RhoD target. We found that RhoD interacts with ZIP kinase in a GTP dependent manner and modulates actin and focal adhesion reorganization. Interestingly, while ectopic expression of ZIPK in fibroblasts induces actin reorganization and actomyosin contraction seen as stress fiber bundling and membrane blebbing, the concomitant expression of active RhoD suppressed this phenotype. Previously, RhoD has been associated with focal adhesion regulation, and in line with this notion, we observed that ZIPK resulted in reorganization of focal adhesion and increased adhesion size. Importantly, the RhoD activity suppressed ZIPK-dependent effects on FAK activity, indicating a functional interplay between RhoD and FAK in the focal adhesion dynamics.
机译:RhoD是经典Rho GTPases的成员,在肌动蛋白动力学的调节中起着至关重要的作用。此外,RhoD还定位于早期的内体和回收内体,这表明在调节内体运输中的其他作用。酵母双杂交筛选确定了拉链相互作用蛋白激酶(ZIPK)为RhoD靶标。我们发现RhoD与GTP依赖方式的ZIP激酶相互作用,并调节肌动蛋白和粘着斑的重组。有趣的是,虽然成纤维细胞中ZIPK的异位表达诱导肌动蛋白重组和肌动球蛋白收缩,如应力纤维束缚和膜起泡,但活性RhoD的伴随表达抑制了该表型。以前,RhoD与粘着斑调节有关,与此相一致,我们观察到ZIPK导致粘着斑的重组和粘连大小的增加。重要的是,RhoD活性抑制了对FAK活性的ZIPK依赖性作用,表明RhoD和FAK在粘着斑动力学中具有功能性相互作用。

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