翻译后修饰:如何调节Rab7的功能。

Q2 Biochemistry, Genetics and Molecular Biology
Small GTPases Pub Date : 2020-05-01 Epub Date: 2018-01-02 DOI:10.1080/21541248.2017.1387686
Graziana Modica, Stephane Lefrancois
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引用次数: 11

摘要

小的GTPase Rab7是内体后期膜运输的主要调节剂。在自噬过程中,这种小GTPase调节内核体到反式高尔基网络的分选受体运输、后期内核体到溶酶体的膜融合以及自噬体到溶酶体的膜融合。与所有Rab7 GTPases一样,Rab7结合下游效应物,协调几种不同的途径。细胞如何调节这些相互作用和下游功能尚不清楚。最近的证据表明,Rab7的功能可以通过几种翻译后修饰的组合来调节,这些修饰促进了与一个效应物的相互作用,同时阻止了与另一个效应物的结合。在这篇综述中,我们讨论了磷酸化、棕榈酰化和泛素化如何调节这种小GTPase在内体晚期协调膜运输的能力的最新数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Post-translational modifications: How to modulate Rab7 functions.

The small GTPase Rab7 is the main regulator of membrane trafficking at late endosomes. This small GTPase regulates endosome-to-trans Golgi Network trafficking of sorting receptors, membrane fusion of late endosomes to lysosomes, and autophagosomes to lysosomes during autophagy. Rab7, like all Rab GTPases, binds downstream effectors coordinating several divergent pathways. How cells regulate these interactions and downstream functions is not well understood. Recent evidence suggests that Rab7 function can be modulated by the combination of several post-translational modifications that facilitate interactions with one effector while preventing binding to another one. In this review, we discuss recent data on how phosphorylation, palmitoylation and ubiquitination modulate the ability of this small GTPase to orchestrate membrane trafficking at the late endosomes.

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来源期刊
Small GTPases
Small GTPases Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
6.10
自引率
0.00%
发文量
6
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