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PNAS Plus: Dual function for Tango1 in secretion of bulky cargo and in ER-Golgi morphology

机译:PNAS Plus:Tango1的双重功能可用于散装货物和ER-高尔基体形态

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摘要

Tango1 enables ER-to-Golgi trafficking of large proteins. We show here that loss of Tango1, in addition to disrupting protein secretion and ER/Golgi morphology, causes ER stress and defects in cell shape. We find that the previously observed dependence of smaller cargos on Tango1 is a secondary effect. If large cargos like Dumpy, which we identify as a Tango1 cargo, are removed from the cell, nonbulky proteins reenter the secretory pathway. Removal of blocking cargo also restores cell morphology and attenuates the ER-stress response. Thus, failures in the secretion of nonbulky proteins, ER stress, and defective cell morphology are secondary consequences of bulky cargo retention. By contrast, ER/Golgi defects in Tango1-depleted cells persist in the absence of bulky cargo, showing that they are due to a secretion-independent function of Tango1. Therefore, maintenance of ER/Golgi architecture and bulky cargo transport are the primary functions for Tango1.
机译:Tango1支持大蛋白从ER到高尔基体的运输。我们在这里显示,Tango1的损失,除了破坏蛋白质分泌和ER /高尔基体形态外,还会引起ER应激和细胞形态缺陷。我们发现先前观察到的较小货物对Tango1的依赖性是次要影响。如果将像Dumpy这样的大杂货(我们认为是Tango1杂货)从细胞中移出,则非大块蛋白会重新进入分泌途径。去除堵塞的货物还可以恢复细胞形态并减弱内质网应激反应。因此,非大块蛋白质的分泌失败,内质网应激和细胞形态缺陷是大量货物滞留的次要结果。相比之下,Tango1耗尽的细胞中的ER /高尔基体缺陷在没有大体积货物的情况下仍然存在,这表明它们是由于Tango1的非分泌依赖性功能所致。因此,维护ER /高尔基架构和大宗货物运输是Tango1的主要功能。

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