YB-1 recruitment to stress granules in zebrafish cells reveals a differential adaptive response to stress

Abstract The survival of cells exposed to adverse environmental conditions entails various alterations in cellular function including major changes in the transcriptome as well as a radical reprogramming of protein translation. While in mammals this process has been extensively studied, stress respo...

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Autores principales: Andrea Maria Guarino, Giuseppe Di Mauro, Gennaro Ruggiero, Nathalie Geyer, Antonella Delicato, Nicholas S. Foulkes, Daniela Vallone, Viola Calabrò
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Publicado: Nature Portfolio 2019
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Acceso en línea:https://doaj.org/article/be8b6eba2b38473b96c65448ebf52a65
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spelling oai:doaj.org-article:be8b6eba2b38473b96c65448ebf52a652021-12-02T15:09:39ZYB-1 recruitment to stress granules in zebrafish cells reveals a differential adaptive response to stress10.1038/s41598-019-45468-62045-2322https://doaj.org/article/be8b6eba2b38473b96c65448ebf52a652019-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-019-45468-6https://doaj.org/toc/2045-2322Abstract The survival of cells exposed to adverse environmental conditions entails various alterations in cellular function including major changes in the transcriptome as well as a radical reprogramming of protein translation. While in mammals this process has been extensively studied, stress responses in non-mammalian vertebrates remain poorly understood. One of the key cellular responses to many different types of stressors is the transient generation of structures called stress granules (SGs). These represent cytoplasmic foci where untranslated mRNAs are sorted or processed for re-initiation, degradation, or packaging into mRNPs. Here, using the evolutionarily conserved Y-box binding protein 1 (YB-1) and G3BP1 as markers, we have studied the formation of stress granules in zebrafish (D. rerio) in response to different environmental stressors. We show that following heat shock, zebrafish cells, like mammalian cells, form stress granules which contain both YB-1 and G3BP1 proteins. Moreover, zfYB-1 knockdown compromises cell viability, as well as recruitment of G3BP1 into SGs, under heat shock conditions highlighting the essential role played by YB-1 in SG assembly and cell survival. However, zebrafish PAC2 cells do not assemble YB-1-positive stress granules upon oxidative stress induced by arsenite, copper or hydrogen peroxide treatment. This contrasts with the situation in human cells where SG formation is robustly induced by exposure to oxidative stressors. Thus, our findings point to fundamental differences in the mechanisms whereby mammalian and zebrafish cells respond to oxidative stress.Andrea Maria GuarinoGiuseppe Di MauroGennaro RuggieroNathalie GeyerAntonella DelicatoNicholas S. FoulkesDaniela ValloneViola CalabròNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Andrea Maria Guarino
Giuseppe Di Mauro
Gennaro Ruggiero
Nathalie Geyer
Antonella Delicato
Nicholas S. Foulkes
Daniela Vallone
Viola Calabrò
YB-1 recruitment to stress granules in zebrafish cells reveals a differential adaptive response to stress
description Abstract The survival of cells exposed to adverse environmental conditions entails various alterations in cellular function including major changes in the transcriptome as well as a radical reprogramming of protein translation. While in mammals this process has been extensively studied, stress responses in non-mammalian vertebrates remain poorly understood. One of the key cellular responses to many different types of stressors is the transient generation of structures called stress granules (SGs). These represent cytoplasmic foci where untranslated mRNAs are sorted or processed for re-initiation, degradation, or packaging into mRNPs. Here, using the evolutionarily conserved Y-box binding protein 1 (YB-1) and G3BP1 as markers, we have studied the formation of stress granules in zebrafish (D. rerio) in response to different environmental stressors. We show that following heat shock, zebrafish cells, like mammalian cells, form stress granules which contain both YB-1 and G3BP1 proteins. Moreover, zfYB-1 knockdown compromises cell viability, as well as recruitment of G3BP1 into SGs, under heat shock conditions highlighting the essential role played by YB-1 in SG assembly and cell survival. However, zebrafish PAC2 cells do not assemble YB-1-positive stress granules upon oxidative stress induced by arsenite, copper or hydrogen peroxide treatment. This contrasts with the situation in human cells where SG formation is robustly induced by exposure to oxidative stressors. Thus, our findings point to fundamental differences in the mechanisms whereby mammalian and zebrafish cells respond to oxidative stress.
format article
author Andrea Maria Guarino
Giuseppe Di Mauro
Gennaro Ruggiero
Nathalie Geyer
Antonella Delicato
Nicholas S. Foulkes
Daniela Vallone
Viola Calabrò
author_facet Andrea Maria Guarino
Giuseppe Di Mauro
Gennaro Ruggiero
Nathalie Geyer
Antonella Delicato
Nicholas S. Foulkes
Daniela Vallone
Viola Calabrò
author_sort Andrea Maria Guarino
title YB-1 recruitment to stress granules in zebrafish cells reveals a differential adaptive response to stress
title_short YB-1 recruitment to stress granules in zebrafish cells reveals a differential adaptive response to stress
title_full YB-1 recruitment to stress granules in zebrafish cells reveals a differential adaptive response to stress
title_fullStr YB-1 recruitment to stress granules in zebrafish cells reveals a differential adaptive response to stress
title_full_unstemmed YB-1 recruitment to stress granules in zebrafish cells reveals a differential adaptive response to stress
title_sort yb-1 recruitment to stress granules in zebrafish cells reveals a differential adaptive response to stress
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/be8b6eba2b38473b96c65448ebf52a65
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