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另一个用于自噬体-溶酶体融合的长 SNARE——Ykt6 如何发挥作用?

Another longin SNARE for autophagosome-lysosome fusion-how does Ykt6 work?

机构信息

a Department of Biochemistry, Yong Loo Lin School of Medicine , National University of Singapore , Singapore.

b NUS Graduate School for Integrative Sciences and Engineering , National University of Singapore , Singapore.

出版信息

Autophagy. 2019 Feb;15(2):352-357. doi: 10.1080/15548627.2018.1532261. Epub 2018 Oct 13.

Abstract

Formation of the autolysosome involves SNARE-mediated autophagosome-lysosome fusion, which is mediated by a combination of the Qa SNARE STX17 (syntaxin 17), the Qbc SNARE SNAP29 and the R-SNAREs VAMP7/8. 2 very recent reports have now implicated another R-SNARE with a longin domain, YKT6, in this fusion process. Interestingly, these reports painted two different pictures of YKT6's involvement. Studies in HeLa cells indicated that YKT6, acting independently of STX17, could form a separate SNARE complex with SNAP29 and another Qa SNARE to mediate autophagosome-lysosome fusion. Conversely, work in larvae fat cells showed that while Ykt6 could form a SNARE complex with Snap29 and Syx17/Stx17, it is readily outcompeted by lysosomal Vamp7 in this regard. Moreover, its activity in autophagosome-lysosome fusion is not impaired by mutation of the supposedly critical ionic zero-layer residue from R to Q. In this regard, YKT6 may therefore act in a noncanonical way to regulate fusion. Here, we ponder on the fresh mechanistic perspectives on the final membrane fusion step of macroautophagy/autophagy offered by these new findings. Further, we propose another possible mechanism as to how YKT6 might act, which may provide some reconciliation to the differences observed. LD: longin domain.

摘要

自噬溶酶体的形成涉及 SNARE 介导的自噬体-溶酶体融合,这是由 Qa SNARE STX17(突触融合蛋白 17)、Qbc SNARE SNAP29 和 R-SNAREs VAMP7/8 的组合介导的。最近的两项研究报告现在表明另一个具有 longin 结构域的 R-SNARE,YKT6,参与了这个融合过程。有趣的是,这些报告描绘了 YKT6 参与的两种不同画面。在 HeLa 细胞中的研究表明,YKT6 可以独立于 STX17 作用,与 SNAP29 和另一个 Qa SNARE 形成独立的 SNARE 复合物,介导自噬体-溶酶体融合。相反,在幼虫脂肪细胞中的工作表明,虽然 Ykt6 可以与 Snap29 和 Syx17/Stx17 形成 SNARE 复合物,但在这方面它很容易被溶酶体 Vamp7 竞争。此外,其在自噬体-溶酶体融合中的活性不会因从 R 突变为 Q 的假定关键离子零层残基的突变而受损。在这方面,YKT6 可能以非典型的方式发挥作用来调节融合。在这里,我们思考了这些新发现为巨自噬/自噬的最终膜融合步骤提供的新的机制观点。此外,我们提出了另一种可能的机制,即 YKT6 可能发挥作用的方式,这可能为观察到的差异提供一些调和。LD:longin 结构域。

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本文引用的文献

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