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Post-Golgi Sec Proteins Are Required for Autophagy in Saccharomyces cerevisiae

机译:高尔基酵母蛋白是酿酒酵母中自噬所必需的

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摘要

In eukaryotic cells, autophagy mediates the degradation of cytosolic contents in response to environmental change. Genetic analyses in fungi have identified over 30 autophagy-related ( ATG ) genes and provide substantial insight into the molecular mechanism of this process. However, one essential issue that has not been resolved is the origin of the lipids that form the autophagosome, the sequestering vesicle that is critical for autophagy. Here, we report that two post-Golgi proteins, Sec2 and Sec4, are required for autophagy. Sec4 is a Rab family GTPase, and Sec2 is its guanine nucleotide exchange factor. In sec2 and sec4 conditional mutant yeast, the anterograde movement of Atg9, a proposed membrane carrier, is impaired during starvation conditions. Similarly, in the sec2 mutant, Atg8 is inefficiently recruited to the phagophore assembly site, which is involved in autophagosome biogenesis, resulting in the generation of fewer autophagosomes. We propose that following autophagy induction the function of Sec2 and Sec4 are diverted to direct membrane flow to autophagosome formation.
机译:在真核细胞中,自噬介导环境变化对胞质含量的降解。真菌的遗传分析已鉴定出30多种自噬相关(ATG)基因,并提供了对该过程的分子机制的实质性了解。然而,尚未解决的一个基本问题是形成自噬体的脂质的起源,自噬体是对自噬至关重要的螯合囊泡。在这里,我们报告自噬需要两个后高尔基体蛋白Sec2和Sec4。 Sec4是Rab家族的GTPase,Sec2是其鸟嘌呤核苷酸交换因子。在sec2和sec4条件突变酵母中,饥饿条件下Atg9(一种拟议的膜载体)的顺行运动受到损害。同样,在sec2突变体中,Atg8无法有效地募集到噬菌体装配位点,该位点与自噬体的生物发生有关,导致产生的自噬体更少。我们建议自噬诱导后,Sec2和Sec4的功能被转移到引导膜流向自噬体形成。

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