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Discovery of Novel Regulators of Autophagy in Animals

The clearance of organelles by autophagy is important for cell health, and defects in this process have been associated with age-associated degenerative disorders. Ubiquitination of proteins enables their recognition by cargo receptors that facilitate the delivery of both protein aggregates and orga...

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Autor principal: Baehrecke, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7743599/
http://dx.doi.org/10.1093/geroni/igaa057.2674
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author Baehrecke, Eric
author_facet Baehrecke, Eric
author_sort Baehrecke, Eric
collection PubMed
description The clearance of organelles by autophagy is important for cell health, and defects in this process have been associated with age-associated degenerative disorders. Ubiquitination of proteins enables their recognition by cargo receptors that facilitate the delivery of both protein aggregates and organelles to forming autophagosomes for degradation. We have investigated developmentally programmed autophagy to identify novel regulators of organelle clearance. We identified an Atg7-independent autophagy program that is required for cell size reduction and clearance of mitochondria. We have used this system to screen for new factors regulate ubiquitin-dependent autophagy and clearance of organelles. We screened a collection of putative ubiquitin binding domain encoding genes, and identified the novel gene Vps13D. Vps13D is an essential gene that is necessary for autophagy, mitochondrial size, mitochondrial clearance, and is associated with human movement disorders. We have used genetics and biochemistry to identify factors that link Vps13D, mitochondrial biology and autophagy.
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spelling pubmed-77435992020-12-21 Discovery of Novel Regulators of Autophagy in Animals Baehrecke, Eric Innov Aging Abstracts The clearance of organelles by autophagy is important for cell health, and defects in this process have been associated with age-associated degenerative disorders. Ubiquitination of proteins enables their recognition by cargo receptors that facilitate the delivery of both protein aggregates and organelles to forming autophagosomes for degradation. We have investigated developmentally programmed autophagy to identify novel regulators of organelle clearance. We identified an Atg7-independent autophagy program that is required for cell size reduction and clearance of mitochondria. We have used this system to screen for new factors regulate ubiquitin-dependent autophagy and clearance of organelles. We screened a collection of putative ubiquitin binding domain encoding genes, and identified the novel gene Vps13D. Vps13D is an essential gene that is necessary for autophagy, mitochondrial size, mitochondrial clearance, and is associated with human movement disorders. We have used genetics and biochemistry to identify factors that link Vps13D, mitochondrial biology and autophagy. Oxford University Press 2020-12-16 /pmc/articles/PMC7743599/ http://dx.doi.org/10.1093/geroni/igaa057.2674 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of The Gerontological Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstracts
Baehrecke, Eric
Discovery of Novel Regulators of Autophagy in Animals
title Discovery of Novel Regulators of Autophagy in Animals
title_full Discovery of Novel Regulators of Autophagy in Animals
title_fullStr Discovery of Novel Regulators of Autophagy in Animals
title_full_unstemmed Discovery of Novel Regulators of Autophagy in Animals
title_short Discovery of Novel Regulators of Autophagy in Animals
title_sort discovery of novel regulators of autophagy in animals
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7743599/
http://dx.doi.org/10.1093/geroni/igaa057.2674
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