Pep12 is important for proteasome microautophagy under low glucose conditions.

microPublication biology Pub Date : 2025-05-07 eCollection Date: 2025-01-01 DOI:10.17912/micropub.biology.001579
Kyle VanderVen, Conner Butcher, Remi' Fokine, Jianhui Li
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引用次数: 0

Abstract

Autophagic degradation of proteasomes is a highly conserved mechanism for regulating proteasome homeostasis in eukaryotes. Here we show that Pep12, a t-SNARE protein, is important for intralumenal vesicle formation in the vacuole and proteasome microautophagy under low glucose conditions. Deleting PEP12 in yeast cells, Saccharomyces cerevisiae , blocked proteasome fragmentation, by which the ESCRT-dependent microautophagy selectively degrades aberrant proteasomes. Accumulation of aberrant proteasomes interfered with proteasome condensate formation in pep12∆ cells. Autophagic bodies were present, but intralumenal vesicles and proteasome microautophagy were absent in the vacuole of pep12∆ cells. Therefore, Pep12 plays an important role in proteasome microautophagy.

在低糖条件下,Pep12对蛋白酶体微自噬很重要。
在真核生物中,蛋白酶体的自噬降解是调节蛋白酶体稳态的高度保守的机制。本研究表明,在低糖条件下,t-SNARE蛋白Pep12在液泡内囊泡形成和蛋白酶体微自噬中起重要作用。在酵母细胞(Saccharomyces cerevisiae)中删除PEP12可以阻断蛋白酶体的断裂,而escrt依赖的微自噬可以选择性地降解异常蛋白酶体。异常蛋白酶体的积累干扰了pep12∆细胞中蛋白酶体凝聚物的形成。自噬小体存在,但在pep12∆细胞的空泡中未见腔内小泡和蛋白酶体微自噬。因此,Pep12在蛋白酶体微自噬中起重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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