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Intersectin-1 interacts with the golgin GCC88 to couple the actin network and Golgi architecture

机译:Intersectin-1与golgin GCC88相互作用以将肌动蛋白网络和高尔基体结构耦合

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摘要

The maintenance of the Golgi ribbon relies on a dynamic balance between the actin and microtubule networks; however, the pathways controlling actin networks remain poorly defined. Previously, we showed that the trans-Golgi network (TGN) membrane tether/golgin, GCC88, modulates the Golgi ribbon architecture. Here, we show that dispersal of the Golgi ribbon by GCC88 is dependent on actin and the involvement of nonmuscle myosin IIA. We have identified the long isoform of intersectin-1 (ITSN-1), a guanine nucleotide exchange factor for Cdc42, as a novel Golgi component and an interaction partner of GCC88 responsible for mediating the actin-dependent dispersal of the Golgi ribbon. We show that perturbation of Golgi morphology by changes in membrane flux, mediated by silencing the retromer subunit Vps26, or in a model of neurodegeneration, induced by Tau overexpression, are also dependent on the ITSN-1-GCC88 interaction. Overall, our study reveals a role for a TGN golgin and ITSN-1 in linking to the actin cytoskeleton and regulating the balance between a compact Golgi ribbon and a dispersed Golgi, a pathway with relevance to pathophysiological conditions.
机译:高尔基带的维持依赖于肌动蛋白和微管网络之间的动态平衡。然而,控制肌动蛋白网络的途径仍然定义不清。先前,我们显示了反高尔基体网络(TGN)膜系带/高尔金体GCC88可以调节高尔基体带结构。在这里,我们表明GCC88的高尔基体功能带的扩散取决于肌动蛋白和非肌肉肌球蛋白IIA的参与。我们已经确定了intersectin-1(ITSN-1),Cdc42的鸟嘌呤核苷酸交换因子的长同工型,作为一种新型的高尔基体成分和GCC88的相互作用伙伴,负责介导高尔基体带的肌动蛋白依赖性分散。我们表明,由膜通量变化引起的高尔基体形态扰动,通过沉默逆转体亚基Vps26介导,或在由Tau过表达诱导的神经变性模型中也依赖于ITSN-1-GCC88相互作用。总的来说,我们的研究揭示了TGN golgin和ITSN-1在连接肌动蛋白细胞骨架和调节致密高尔基体带与分散高尔基体之间的平衡方面的作用,该途径与病理生理状况相关。

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