细胞器间竞价战:竞争性细胞器特异性适配器的Vps13定位

Contact Pub Date : 2018-11-27 DOI:10.1177/2515256418814621
Samantha K. Dziurdzik, Björn D. M. Bean, E. Conibear
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引用次数: 1

摘要

膜接触部位是通过控制组成蛋白的招募来调节的。酵母液泡蛋白分选13 (Vps13)在不同的细胞条件下动态定位于核内体、液泡、线粒体和内质网的膜接触位点,并在减数分裂期间被招募到前体膜上。在我们最近的工作之前,接触部位定位的机制在很大程度上是未知的。我们发现Ypt35是核内体和核-液泡连接的新型Vps13接头。此外,我们在Ypt35中发现了一个保守的募集基序,并在前体膜和线粒体接头Spo71和Mcp1中分别发现了相关的基序。所有三个适配器竞争结合到Vps13的六重复区域,表明适配器竞争调节Vps13的定位。在这里,我们总结和讨论了我们工作的意义,突出了关键的悬而未决的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Interorganellar Bidding War: Vps13 Localization by Competitive Organelle-Specific Adaptors
Membrane contact sites are regulated through the controlled recruitment of constituent proteins. Yeast vacuolar protein sorting 13 (Vps13) dynamically localizes to membrane contact sites at endosomes, vacuoles, mitochondria, and the endoplasmic reticulum under different cellular conditions and is recruited to the prospore membrane during meiosis. Prior to our recent work, the mechanism for localization at contact sites was largely unknown. We identified Ypt35 as a novel Vps13 adaptor for endosomes and the nucleus-vacuole junction. Furthermore, we discovered a conserved recruitment motif in Ypt35 and found related motifs in the prospore membrane and mitochondrial adaptors, Spo71 and Mcp1, respectively. All three adaptors compete for binding to a six-repeat region of Vps13, suggesting adaptor competition regulates Vps13 localization. Here, we summarize and discuss the implications of our work, highlighting key outstanding questions.
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