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Assays to Monitor Autophagy in Saccharomyces cerevisiae

Autophagy is an intracellular process responsible for the degradation and recycling of cytoplasmic components. It selectively removes harmful cellular material and enables the cell to survive starvation by mobilizing nutrients via the bulk degradation of cytoplasmic components. While research over t...

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Detalles Bibliográficos
Autores principales: Torggler, Raffaela, Papinski, Daniel, Kraft, Claudine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617969/
https://www.ncbi.nlm.nih.gov/pubmed/28703742
http://dx.doi.org/10.3390/cells6030023
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author Torggler, Raffaela
Papinski, Daniel
Kraft, Claudine
author_facet Torggler, Raffaela
Papinski, Daniel
Kraft, Claudine
author_sort Torggler, Raffaela
collection PubMed
description Autophagy is an intracellular process responsible for the degradation and recycling of cytoplasmic components. It selectively removes harmful cellular material and enables the cell to survive starvation by mobilizing nutrients via the bulk degradation of cytoplasmic components. While research over the last decades has led to the discovery of the key factors involved in autophagy, the pathway is not yet completely understood. The first studies of autophagy on a molecular level were conducted in the yeast Saccharomyces cerevisiae. Building up on these studies, many homologs have been found in higher eukaryotes. Yeast remains a highly relevant model organism for studying autophagy, with a wide range of established methods to elucidate the molecular details of the autophagy pathway. In this review, we provide an overview of methods to study both selective and bulk autophagy, including intermediate steps in the yeast Saccharomyces cerevisiae. We compare different assays, discuss their advantages and limitations and list potential applications.
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spelling pubmed-56179692017-09-29 Assays to Monitor Autophagy in Saccharomyces cerevisiae Torggler, Raffaela Papinski, Daniel Kraft, Claudine Cells Review Autophagy is an intracellular process responsible for the degradation and recycling of cytoplasmic components. It selectively removes harmful cellular material and enables the cell to survive starvation by mobilizing nutrients via the bulk degradation of cytoplasmic components. While research over the last decades has led to the discovery of the key factors involved in autophagy, the pathway is not yet completely understood. The first studies of autophagy on a molecular level were conducted in the yeast Saccharomyces cerevisiae. Building up on these studies, many homologs have been found in higher eukaryotes. Yeast remains a highly relevant model organism for studying autophagy, with a wide range of established methods to elucidate the molecular details of the autophagy pathway. In this review, we provide an overview of methods to study both selective and bulk autophagy, including intermediate steps in the yeast Saccharomyces cerevisiae. We compare different assays, discuss their advantages and limitations and list potential applications. MDPI 2017-07-13 /pmc/articles/PMC5617969/ /pubmed/28703742 http://dx.doi.org/10.3390/cells6030023 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Torggler, Raffaela
Papinski, Daniel
Kraft, Claudine
Assays to Monitor Autophagy in Saccharomyces cerevisiae
title Assays to Monitor Autophagy in Saccharomyces cerevisiae
title_full Assays to Monitor Autophagy in Saccharomyces cerevisiae
title_fullStr Assays to Monitor Autophagy in Saccharomyces cerevisiae
title_full_unstemmed Assays to Monitor Autophagy in Saccharomyces cerevisiae
title_short Assays to Monitor Autophagy in Saccharomyces cerevisiae
title_sort assays to monitor autophagy in saccharomyces cerevisiae
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617969/
https://www.ncbi.nlm.nih.gov/pubmed/28703742
http://dx.doi.org/10.3390/cells6030023
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