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Arabidopsis cargo receptor NBR1 mediates selective autophagy of defective proteins

Aggrephagy, a type of selective autophagy that sequesters protein aggregates for degradation in the vacuole, is an important protein quality control mechanism, particularly during cell stress. In mammalian cells, aggrephagy and several other forms of selective autophagy are mediated by dedicated car...

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Autores principales: Jung, Hyera, Lee, Han Nim, Marshall, Richard S, Lomax, Aaron W, Yoon, Min Ji, Kim, Jimi, Kim, Jeong Hun, Vierstra, Richard D, Chung, Taijoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913707/
https://www.ncbi.nlm.nih.gov/pubmed/31494674
http://dx.doi.org/10.1093/jxb/erz404
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author Jung, Hyera
Lee, Han Nim
Marshall, Richard S
Lomax, Aaron W
Yoon, Min Ji
Kim, Jimi
Kim, Jeong Hun
Vierstra, Richard D
Chung, Taijoon
author_facet Jung, Hyera
Lee, Han Nim
Marshall, Richard S
Lomax, Aaron W
Yoon, Min Ji
Kim, Jimi
Kim, Jeong Hun
Vierstra, Richard D
Chung, Taijoon
author_sort Jung, Hyera
collection PubMed
description Aggrephagy, a type of selective autophagy that sequesters protein aggregates for degradation in the vacuole, is an important protein quality control mechanism, particularly during cell stress. In mammalian cells, aggrephagy and several other forms of selective autophagy are mediated by dedicated cargo receptors such as NEIGHBOR OF BRCA1 (NBR1). Although plant NBR1 homologs have been linked to selective autophagy during biotic stress, it remains unclear how they impact selective autophagy under non-stressed and abiotic stress conditions. Through microscopic and biochemical analysis of nbr1 mutants expressing autophagy markers and an aggregation-prone reporter, we tested the connection between NBR1 and aggrephagy in Arabidopsis. Although NBR1 is not essential for general autophagy, or for the selective clearance of peroxisomes, mitochondria, or the ER, we found that NBR1 is required for the heat-induced formation of autophagic vesicles. Moreover, cytoplasmic puncta containing aggregation-prone proteins, which were rarely observed in wild-type plants, were found to accumulate in nbr1 mutants under both control and heat stress conditions. Given that NBR1 co-localizes with these cytoplasmic puncta, we propose that Arabidopsis NBR1 is a plant aggrephagy receptor essential for maintaining proteostasis under both heat stress and non-stress conditions.
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spelling pubmed-69137072019-12-19 Arabidopsis cargo receptor NBR1 mediates selective autophagy of defective proteins Jung, Hyera Lee, Han Nim Marshall, Richard S Lomax, Aaron W Yoon, Min Ji Kim, Jimi Kim, Jeong Hun Vierstra, Richard D Chung, Taijoon J Exp Bot Research Papers Aggrephagy, a type of selective autophagy that sequesters protein aggregates for degradation in the vacuole, is an important protein quality control mechanism, particularly during cell stress. In mammalian cells, aggrephagy and several other forms of selective autophagy are mediated by dedicated cargo receptors such as NEIGHBOR OF BRCA1 (NBR1). Although plant NBR1 homologs have been linked to selective autophagy during biotic stress, it remains unclear how they impact selective autophagy under non-stressed and abiotic stress conditions. Through microscopic and biochemical analysis of nbr1 mutants expressing autophagy markers and an aggregation-prone reporter, we tested the connection between NBR1 and aggrephagy in Arabidopsis. Although NBR1 is not essential for general autophagy, or for the selective clearance of peroxisomes, mitochondria, or the ER, we found that NBR1 is required for the heat-induced formation of autophagic vesicles. Moreover, cytoplasmic puncta containing aggregation-prone proteins, which were rarely observed in wild-type plants, were found to accumulate in nbr1 mutants under both control and heat stress conditions. Given that NBR1 co-localizes with these cytoplasmic puncta, we propose that Arabidopsis NBR1 is a plant aggrephagy receptor essential for maintaining proteostasis under both heat stress and non-stress conditions. Oxford University Press 2020-01-01 2019-09-08 /pmc/articles/PMC6913707/ /pubmed/31494674 http://dx.doi.org/10.1093/jxb/erz404 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Papers
Jung, Hyera
Lee, Han Nim
Marshall, Richard S
Lomax, Aaron W
Yoon, Min Ji
Kim, Jimi
Kim, Jeong Hun
Vierstra, Richard D
Chung, Taijoon
Arabidopsis cargo receptor NBR1 mediates selective autophagy of defective proteins
title Arabidopsis cargo receptor NBR1 mediates selective autophagy of defective proteins
title_full Arabidopsis cargo receptor NBR1 mediates selective autophagy of defective proteins
title_fullStr Arabidopsis cargo receptor NBR1 mediates selective autophagy of defective proteins
title_full_unstemmed Arabidopsis cargo receptor NBR1 mediates selective autophagy of defective proteins
title_short Arabidopsis cargo receptor NBR1 mediates selective autophagy of defective proteins
title_sort arabidopsis cargo receptor nbr1 mediates selective autophagy of defective proteins
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913707/
https://www.ncbi.nlm.nih.gov/pubmed/31494674
http://dx.doi.org/10.1093/jxb/erz404
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