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Regulation of autophagy by the Rab GTPase network

机译:Rab GTPase网络对自噬的调节

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Autophagy (macroautophagy) is a highly conserved intracellular and lysosome-dependent degradation process in which autophagic substrates are enclosed and degraded by a double-membrane vesicular structure in a continuous and dynamic vesicle transport process. The Rab protein is a small GTPase that belongs to the Ras-like GTPase superfamily and regulates the vesicle traffic process. Numerous Rab proteins have been shown to be involved in various stages of autophagy. Rab1, Rab5, Rab7, Rab9A, Rab11, Rab23, Rab32, and Rab33B participate in autophagosome formation, whereas Rab9 is required in non-canonical autophagy. Rab7, Rab8B, and Rab24 have a key role in autophagosome maturation. Rab8A and Rab25 are also involved in autophagy, but their role is unknown. Here, we summarize new findings regarding the involvement of Rabs in autophagy and provide insights regarding future research on the mechanisms of autophagy regulation.
机译:自噬(宏观自噬)是高度保守的细胞内和溶酶体依赖性降解过程,其中自噬基质被双膜囊泡结构封闭并在连续且动态的囊泡转运过程中降解。 Rab蛋白是一种小GTP酶,属于Ras样GTPase超家族,可调节囊泡运输过程。已显示许多Rab蛋白参与自噬的各个阶段。 Rab1,Rab5,Rab7,Rab9A,Rab11,Rab23,Rab32和Rab33B参与自噬小体的形成,而Rab9在非规范自噬中是必需的。 Rab7,Rab8B和Rab24在自噬小体成熟中起关键作用。 Rab8A和Rab25也参与自噬,但它们的作用尚不清楚。在这里,我们总结了有关Rabs参与自噬的新发现,并提供了有关自噬调节机制未来研究的见识。

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