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Stress induced nuclear granules form in response to accumulation of misfolded proteins in Caenorhabditis elegans
BACKGROUND: Environmental stress can affect the viability or fecundity of an organism. Environmental stressors may affect the genome or the proteome and can cause cellular distress by contributing to protein damage or misfolding. This study examines the cellular response to environmental stress in t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395811/ https://www.ncbi.nlm.nih.gov/pubmed/28424053 http://dx.doi.org/10.1186/s12860-017-0136-x |
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author | Sampuda, Katherine M. Riley, Mason Boyd, Lynn |
author_facet | Sampuda, Katherine M. Riley, Mason Boyd, Lynn |
author_sort | Sampuda, Katherine M. |
collection | PubMed |
description | BACKGROUND: Environmental stress can affect the viability or fecundity of an organism. Environmental stressors may affect the genome or the proteome and can cause cellular distress by contributing to protein damage or misfolding. This study examines the cellular response to environmental stress in the germline of the nematode, C. elegans. RESULTS: Salt stress, oxidative stress, and starvation, but not heat shock, induce the relocalization of ubiquitin, proteasome, and the TIAR-2 protein into distinct subnuclear regions referred to as stress induced nuclear granules (SINGs). The SINGs form within 1 h of stress initiation and do not require intertissue signaling. K48-linked polyubiquitin chains but not K63 chains are enriched in SINGs. Worms with a mutation in the conjugating enzyme, ubc-18, do not form SINGs. Additionally, knockdown of ubc-20 and ubc-22 reduces the level of SING formation as does knockdown of the ubiquitin ligase chn-1, a CHIP homolog. The nuclear import machinery is required for SING formation. Stressed embryos containing SINGs fail to hatch and cell division in these embryos is halted. The formation of SINGs can be prevented by pre-exposure to a brief period of heat shock before stress exposure. Heat shock inhibition of SINGs is dependent upon the HSF-1 transcription factor. CONCLUSIONS: The heat shock results suggest that chaperone expression can prevent SING formation and that the accumulation of damaged or misfolded proteins is a necessary precursor to SING formation. Thus, SINGs may be part of a novel protein quality control system. The data suggest an interesting model where SINGs represent sites of localized protein degradation for nuclear or cytosolic proteins. Thus, the physiological impacts of environmental stress may begin at the cellular level with the formation of stress induced nuclear granules. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12860-017-0136-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5395811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53958112017-04-20 Stress induced nuclear granules form in response to accumulation of misfolded proteins in Caenorhabditis elegans Sampuda, Katherine M. Riley, Mason Boyd, Lynn BMC Cell Biol Research Article BACKGROUND: Environmental stress can affect the viability or fecundity of an organism. Environmental stressors may affect the genome or the proteome and can cause cellular distress by contributing to protein damage or misfolding. This study examines the cellular response to environmental stress in the germline of the nematode, C. elegans. RESULTS: Salt stress, oxidative stress, and starvation, but not heat shock, induce the relocalization of ubiquitin, proteasome, and the TIAR-2 protein into distinct subnuclear regions referred to as stress induced nuclear granules (SINGs). The SINGs form within 1 h of stress initiation and do not require intertissue signaling. K48-linked polyubiquitin chains but not K63 chains are enriched in SINGs. Worms with a mutation in the conjugating enzyme, ubc-18, do not form SINGs. Additionally, knockdown of ubc-20 and ubc-22 reduces the level of SING formation as does knockdown of the ubiquitin ligase chn-1, a CHIP homolog. The nuclear import machinery is required for SING formation. Stressed embryos containing SINGs fail to hatch and cell division in these embryos is halted. The formation of SINGs can be prevented by pre-exposure to a brief period of heat shock before stress exposure. Heat shock inhibition of SINGs is dependent upon the HSF-1 transcription factor. CONCLUSIONS: The heat shock results suggest that chaperone expression can prevent SING formation and that the accumulation of damaged or misfolded proteins is a necessary precursor to SING formation. Thus, SINGs may be part of a novel protein quality control system. The data suggest an interesting model where SINGs represent sites of localized protein degradation for nuclear or cytosolic proteins. Thus, the physiological impacts of environmental stress may begin at the cellular level with the formation of stress induced nuclear granules. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12860-017-0136-x) contains supplementary material, which is available to authorized users. BioMed Central 2017-04-19 /pmc/articles/PMC5395811/ /pubmed/28424053 http://dx.doi.org/10.1186/s12860-017-0136-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Sampuda, Katherine M. Riley, Mason Boyd, Lynn Stress induced nuclear granules form in response to accumulation of misfolded proteins in Caenorhabditis elegans |
title | Stress induced nuclear granules form in response to accumulation of misfolded proteins in Caenorhabditis elegans |
title_full | Stress induced nuclear granules form in response to accumulation of misfolded proteins in Caenorhabditis elegans |
title_fullStr | Stress induced nuclear granules form in response to accumulation of misfolded proteins in Caenorhabditis elegans |
title_full_unstemmed | Stress induced nuclear granules form in response to accumulation of misfolded proteins in Caenorhabditis elegans |
title_short | Stress induced nuclear granules form in response to accumulation of misfolded proteins in Caenorhabditis elegans |
title_sort | stress induced nuclear granules form in response to accumulation of misfolded proteins in caenorhabditis elegans |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5395811/ https://www.ncbi.nlm.nih.gov/pubmed/28424053 http://dx.doi.org/10.1186/s12860-017-0136-x |
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