一种基于荧光激活细胞分选(FACS)的新型筛选方法发现了ATG14,它是甲基营养酵母中进行pexophagy所需的基因。

IF 2.4 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Kosuke Shiraishi, Yumi Arima, Motoharu Nakamura, Takumi Nakatsuji, Masahide Oku, Yasuyoshi Sakai
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引用次数: 0

摘要

自噬是一种选择性降解过氧化物酶体的自噬方式,可分为大自噬和小自噬。在大吞噬过程中,单个过氧物酶体被嗜酸酶体封存,并被运送到液泡中降解;而在微吞噬过程中,过氧物酶体直接被有隔膜的液泡吞噬。迄今为止,一些自噬相关基因(ATGs)主要是在微吞噬诱导条件下通过平板检测鉴定出来的。在这里,我们利用荧光激活细胞分选技术(FACS)开发了一种新型高通量筛选系统,用于鉴定大吞噬作用所需的基因。利用该系统,我们发现了 KpATG14,由于技术限制,该基因之前未能在养甲酵母 Komagataella phaffii 中被鉴定出来。显微镜和免疫印迹分析发现,KpAtg14 是大吞噬作用和小吞噬作用的必需基因。我们还发现,KpAtg14 是在前自噬体结构(PAS)招募下游因子 KpAtg5 的必要条件,因此也是大量自噬的必要条件。我们预计,我们的检测方法将用于鉴定大体积自噬所需的新基因,从而更好地了解过氧化物酶体现有的两种自噬降解途径的生理意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel fluorescence-activated cell sorting (FACS)-based screening identified ATG14, the gene required for pexophagy in the methylotrophic yeast.

Pexophagy is a type of autophagy that selectively degrades peroxisomes and can be classified as either macropexophagy or micropexophagy. During macropexophagy, individual peroxisomes are sequestered by pexophagosomes and transported to the vacuole for degradation, while in micropexophagy, peroxisomes are directly engulfed by the septated vacuole. To date, some autophagy-related genes (ATGs) required for pexophagy have been identified through plate-based assays performed primarily under micropexophagy-induced conditions. Here, we developed a novel high-throughput screening system using fluorescence-activated cell sorting (FACS) to identify genes required for macropexophagy. Using this system, we discovered KpATG14, a gene that could not be identified previously in the methylotrophic yeast Komagataella phaffii due to technical limitations. Microscopic and immunoblot analyses found that KpAtg14 was required for both macropexophagy and micropexophagy. We also revealed that KpAtg14 was necessary for recruitment of the downstream factor KpAtg5 at the preautophagosomal structure (PAS), and consequently, for bulk autophagy. We anticipate our assay to be used to identify novel genes that are exclusively required for macropexophagy, leading to better understanding of the physiological significance of the existing two types of autophagic degradation pathways for peroxisomes.

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来源期刊
FEMS yeast research
FEMS yeast research 生物-生物工程与应用微生物
CiteScore
5.70
自引率
6.20%
发文量
54
审稿时长
1 months
期刊介绍: FEMS Yeast Research offers efficient publication of high-quality original Research Articles, Mini-reviews, Letters to the Editor, Perspectives and Commentaries that express current opinions. The journal will select for publication only those manuscripts deemed to be of major relevance to the field and generally will not consider articles that are largely descriptive without insights on underlying mechanism or biology. Submissions on any yeast species are welcome provided they report results within the scope outlined below and are of significance to the yeast field.
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