Re-exploration of all <i>ATG</i> genes

Most autophagy-related (<i>ATG</i>) genes have been identified and characterized through studies using the budding yeast <i>Saccharomyces cerevisiae</i>. However, there are no studies that comprehensively compare the contribution of each <i>ATG</i> gene to non-selective bulk autophagy and various types of selective autophagy, including the cytoplasm-to-vacuole targeting (Cvt) pathway, mitophagy, reticulophagy, and pexophagy. Our recent study quantified these types of autophagy in all <i>atg</i> mutants and showed that (i) autophagy is not completely impaired in specific deletants such as lacking the components of the two ubiquitin conjugation-like (UBL) systems, traditionally regarded as essential for autophagy in yeast, and (ii) residual autophagic activity is especially prominent in mutants of the Atg8 UBL system, which display small autophagic body-like vesicles at a low frequency. Alongside these findings, our comprehensive analysis suggested a link between mitophagy and pexophagy, and a differential contribution of Atg proteins to cargo specificity. We discuss how our datasets are useful for future autophagy research. <b>Abbreviations:</b> Ape1: aminopeptidase I; ATG: autophagy related; Cvt: cytoplasm-to-vacuole targeting; ER: endoplasmic reticulum; ESCRT: endosomal sorting complex required for transport; GFP: green fluorescent protein; PI3K: phosphatidylinositol 3-kinase; UBL: ubiquitin conjugation-like.

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Publication Details

Journal
Autophagy Reports
Published
2024-08-26
DOI
https://doi.org/10.1080/27694127.2024.2386194
Citations
2
Primary Topic
Ubiquitin and proteasome pathways
Type
article
Field-Weighted Citation Impact
0.47

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article

Re-exploration of all ATG genes

Kentaro Furukawa, Tomotake Kanki, Tamara Ginevskaia
2 citations
Autophagy Reports
Ubiquitin and proteasome pathways
0.47
article

Re-exploration of all ATG genes

Kentaro Furukawa, Tomotake Kanki, Tamara Ginevskaia
article en
2 citations

Abstract

Most autophagy-related (<i>ATG</i>) genes have been identified and characterized through studies using the budding yeast <i>Saccharomyces cerevisiae</i>. However, there are no studies that comprehensively compare the contribution of each <i>ATG</i> gene to non-selective bulk autophagy and various types of selective autophagy, including the cytoplasm-to-vacuole targeting (Cvt) pathway, mitophagy, reticulophagy, and pexophagy. Our recent study quantified these types of autophagy in all <i>atg</i> mutants and showed that (i) autophagy is not completely impaired in specific deletants such as lacking the components of the two ubiquitin conjugation-like (UBL) systems, traditionally regarded as essential for autophagy in yeast, and (ii) residual autophagic activity is especially prominent in mutants of the Atg8 UBL system, which display small autophagic body-like vesicles at a low frequency. Alongside these findings, our comprehensive analysis suggested a link between mitophagy and pexophagy, and a differential contribution of Atg proteins to cargo specificity. We discuss how our datasets are useful for future autophagy research. <b>Abbreviations:</b> Ape1: aminopeptidase I; ATG: autophagy related; Cvt: cytoplasm-to-vacuole targeting; ER: endoplasmic reticulum; ESCRT: endosomal sorting complex required for transport; GFP: green fluorescent protein; PI3K: phosphatidylinositol 3-kinase; UBL: ubiquitin conjugation-like.

Autophagy ReportsVol. 3(1)
Kyushu University (JP), Niigata University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 36%
Ubiquitin and proteasome pathways
0.47
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