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秀丽隐杆线虫筛选鉴定出专属于多细胞生物的自噬基因。

C. elegans screen identifies autophagy genes specific to multicellular organisms.

机构信息

National Institute of Biological Sciences, Beijing 102206, P.R. China.

出版信息

Cell. 2010 Jun 11;141(6):1042-55. doi: 10.1016/j.cell.2010.04.034.

Abstract

The molecular understanding of autophagy has originated almost exclusively from yeast genetic studies. Little is known about essential autophagy components specific to higher eukaryotes. Here we perform genetic screens in C. elegans and identify four metazoan-specific autophagy genes, named epg-2, -3, -4, and -5. Genetic analysis reveals that epg-2, -3, -4, and -5 define discrete genetic steps of the autophagy pathway. epg-2 encodes a coiled-coil protein that functions in specific autophagic cargo recognition. Mammalian homologs of EPG-3/VMP1, EPG-4/EI24, and EPG-5/mEPG5 are essential for starvation-induced autophagy. VMP1 regulates autophagosome formation by controlling the duration of omegasomes. EI24 and mEPG5 are required for formation of degradative autolysosomes. This study establishes C. elegans as a multicellular genetic model to delineate the autophagy pathway and provides mechanistic insights into the metazoan-specific autophagic process.

摘要

自噬的分子机制几乎完全源自于酵母的遗传学研究。人们对高等真核生物特有的必需自噬成分知之甚少。在这里,我们在秀丽隐杆线虫中进行了遗传筛选,并鉴定了四个后生动物特异性自噬基因,分别命名为 epg-2、-3、-4 和 -5。遗传分析表明,epg-2、-3、-4 和 -5 定义了自噬途径的离散遗传步骤。epg-2 编码一种卷曲螺旋蛋白,在特定的自噬货物识别中发挥作用。哺乳动物 EPG-3/VMP1、EPG-4/EI24 和 EPG-5/mEPG5 的同源物对于饥饿诱导的自噬是必需的。VMP1 通过控制 omegasomes 的持续时间来调节自噬体的形成。EI24 和 mEPG5 对于降解性自溶体的形成是必需的。本研究确立了秀丽隐杆线虫作为一个多细胞遗传模型,以描绘自噬途径,并为后生动物特异性自噬过程提供了机制上的见解。

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