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Proteasome β5 subunit overexpression improves proteostasis during aging and extends lifespan in Drosophila melanogaster

The β5 subunit of the proteasome has been shown in worms and in human cell lines to be regulatory. In these models, β5 overexpression results in upregulation of the entire proteasome complex which is sufficient to increase proteotoxic stress resistance, improve metabolic parameters, and increase lon...

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Autores principales: Nguyen, Nga N., Rana, Anil, Goldman, Camille, Moore, Rhiannon, Tai, Justin, Hong, Yongchan, Shen, Jingyi, Walker, David W., Hur, Jae H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395709/
https://www.ncbi.nlm.nih.gov/pubmed/30816680
http://dx.doi.org/10.1038/s41598-019-39508-4
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author Nguyen, Nga N.
Rana, Anil
Goldman, Camille
Moore, Rhiannon
Tai, Justin
Hong, Yongchan
Shen, Jingyi
Walker, David W.
Hur, Jae H.
author_facet Nguyen, Nga N.
Rana, Anil
Goldman, Camille
Moore, Rhiannon
Tai, Justin
Hong, Yongchan
Shen, Jingyi
Walker, David W.
Hur, Jae H.
author_sort Nguyen, Nga N.
collection PubMed
description The β5 subunit of the proteasome has been shown in worms and in human cell lines to be regulatory. In these models, β5 overexpression results in upregulation of the entire proteasome complex which is sufficient to increase proteotoxic stress resistance, improve metabolic parameters, and increase longevity. However, fundamental questions remain unanswered, including the temporal requirements for β5 overexpression and whether β5 overexpression can extend lifespan in other species. To determine if adult-only overexpression of the β5 subunit can increase proteasome activity in a different model, we characterized phenotypes associated with β5 overexpression in Drosophila melanogaster adults. We find that adult-only overexpression of the β5 subunit does not result in transcriptional upregulation of the other subunits of the proteasome as they do in nematodes and human cell culture. Despite this lack of a regulatory role, boosting β5 expression increases the chymotrypsin-like activity associated with the proteasome, reduces both the size and number of ubiquitinated protein aggregates in aged flies, and increases longevity. Surprisingly, these phenotypes were not associated with increased resistance to acute proteotoxic insults or improved metabolic parameters.
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spelling pubmed-63957092019-03-04 Proteasome β5 subunit overexpression improves proteostasis during aging and extends lifespan in Drosophila melanogaster Nguyen, Nga N. Rana, Anil Goldman, Camille Moore, Rhiannon Tai, Justin Hong, Yongchan Shen, Jingyi Walker, David W. Hur, Jae H. Sci Rep Article The β5 subunit of the proteasome has been shown in worms and in human cell lines to be regulatory. In these models, β5 overexpression results in upregulation of the entire proteasome complex which is sufficient to increase proteotoxic stress resistance, improve metabolic parameters, and increase longevity. However, fundamental questions remain unanswered, including the temporal requirements for β5 overexpression and whether β5 overexpression can extend lifespan in other species. To determine if adult-only overexpression of the β5 subunit can increase proteasome activity in a different model, we characterized phenotypes associated with β5 overexpression in Drosophila melanogaster adults. We find that adult-only overexpression of the β5 subunit does not result in transcriptional upregulation of the other subunits of the proteasome as they do in nematodes and human cell culture. Despite this lack of a regulatory role, boosting β5 expression increases the chymotrypsin-like activity associated with the proteasome, reduces both the size and number of ubiquitinated protein aggregates in aged flies, and increases longevity. Surprisingly, these phenotypes were not associated with increased resistance to acute proteotoxic insults or improved metabolic parameters. Nature Publishing Group UK 2019-02-28 /pmc/articles/PMC6395709/ /pubmed/30816680 http://dx.doi.org/10.1038/s41598-019-39508-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Nguyen, Nga N.
Rana, Anil
Goldman, Camille
Moore, Rhiannon
Tai, Justin
Hong, Yongchan
Shen, Jingyi
Walker, David W.
Hur, Jae H.
Proteasome β5 subunit overexpression improves proteostasis during aging and extends lifespan in Drosophila melanogaster
title Proteasome β5 subunit overexpression improves proteostasis during aging and extends lifespan in Drosophila melanogaster
title_full Proteasome β5 subunit overexpression improves proteostasis during aging and extends lifespan in Drosophila melanogaster
title_fullStr Proteasome β5 subunit overexpression improves proteostasis during aging and extends lifespan in Drosophila melanogaster
title_full_unstemmed Proteasome β5 subunit overexpression improves proteostasis during aging and extends lifespan in Drosophila melanogaster
title_short Proteasome β5 subunit overexpression improves proteostasis during aging and extends lifespan in Drosophila melanogaster
title_sort proteasome β5 subunit overexpression improves proteostasis during aging and extends lifespan in drosophila melanogaster
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395709/
https://www.ncbi.nlm.nih.gov/pubmed/30816680
http://dx.doi.org/10.1038/s41598-019-39508-4
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