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SUMOylation of the nuclear pore complex basket is involved in sensing cellular stresses

The nuclear pore complex (NPC) is the major conduit for nucleocytoplasmic transport and serves as a platform for gene regulation and DNA repair. Several nucleoporins undergo ubiquitylation and SUMOylation, and these modifications play an important role in nuclear pore dynamics and plasticity. Here,...

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Autores principales: Folz, Hanne, Niño, Carlos A., Taranum, Surayya, Caesar, Stefanie, Latta, Lorenz, Waharte, François, Salamero, Jean, Schlenstedt, Gabriel, Dargemont, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467484/
https://www.ncbi.nlm.nih.gov/pubmed/30837289
http://dx.doi.org/10.1242/jcs.224279
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author Folz, Hanne
Niño, Carlos A.
Taranum, Surayya
Caesar, Stefanie
Latta, Lorenz
Waharte, François
Salamero, Jean
Schlenstedt, Gabriel
Dargemont, Catherine
author_facet Folz, Hanne
Niño, Carlos A.
Taranum, Surayya
Caesar, Stefanie
Latta, Lorenz
Waharte, François
Salamero, Jean
Schlenstedt, Gabriel
Dargemont, Catherine
author_sort Folz, Hanne
collection PubMed
description The nuclear pore complex (NPC) is the major conduit for nucleocytoplasmic transport and serves as a platform for gene regulation and DNA repair. Several nucleoporins undergo ubiquitylation and SUMOylation, and these modifications play an important role in nuclear pore dynamics and plasticity. Here, we perform a detailed analysis of these post-translational modifications of yeast nuclear basket proteins under normal growth conditions as well as upon cellular stresses, with a focus on SUMOylation. We find that the balance between the dynamics of SUMOylation and deSUMOylation of Nup60 and Nup2 at the NPC differs substantially, particularly in G1 and S phase. While Nup60 is the unique target of genotoxic stress within the nuclear basket that probably belongs to the SUMO-mediated DNA damage response pathway, both Nup2 and Nup60 show a dramatic increase in SUMOylation upon osmotic stress, with Nup2 SUMOylation being enhanced in Nup60 SUMO-deficient mutant yeast strains. Taken together, our data reveal that there are several levels of crosstalk between nucleoporins, and that the post-translational modifications of the NPC serve in sensing cellular stress signals.
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spelling pubmed-64674842019-04-30 SUMOylation of the nuclear pore complex basket is involved in sensing cellular stresses Folz, Hanne Niño, Carlos A. Taranum, Surayya Caesar, Stefanie Latta, Lorenz Waharte, François Salamero, Jean Schlenstedt, Gabriel Dargemont, Catherine J Cell Sci Research Article The nuclear pore complex (NPC) is the major conduit for nucleocytoplasmic transport and serves as a platform for gene regulation and DNA repair. Several nucleoporins undergo ubiquitylation and SUMOylation, and these modifications play an important role in nuclear pore dynamics and plasticity. Here, we perform a detailed analysis of these post-translational modifications of yeast nuclear basket proteins under normal growth conditions as well as upon cellular stresses, with a focus on SUMOylation. We find that the balance between the dynamics of SUMOylation and deSUMOylation of Nup60 and Nup2 at the NPC differs substantially, particularly in G1 and S phase. While Nup60 is the unique target of genotoxic stress within the nuclear basket that probably belongs to the SUMO-mediated DNA damage response pathway, both Nup2 and Nup60 show a dramatic increase in SUMOylation upon osmotic stress, with Nup2 SUMOylation being enhanced in Nup60 SUMO-deficient mutant yeast strains. Taken together, our data reveal that there are several levels of crosstalk between nucleoporins, and that the post-translational modifications of the NPC serve in sensing cellular stress signals. The Company of Biologists Ltd 2019-04-01 2019-04-03 /pmc/articles/PMC6467484/ /pubmed/30837289 http://dx.doi.org/10.1242/jcs.224279 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This 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 use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Folz, Hanne
Niño, Carlos A.
Taranum, Surayya
Caesar, Stefanie
Latta, Lorenz
Waharte, François
Salamero, Jean
Schlenstedt, Gabriel
Dargemont, Catherine
SUMOylation of the nuclear pore complex basket is involved in sensing cellular stresses
title SUMOylation of the nuclear pore complex basket is involved in sensing cellular stresses
title_full SUMOylation of the nuclear pore complex basket is involved in sensing cellular stresses
title_fullStr SUMOylation of the nuclear pore complex basket is involved in sensing cellular stresses
title_full_unstemmed SUMOylation of the nuclear pore complex basket is involved in sensing cellular stresses
title_short SUMOylation of the nuclear pore complex basket is involved in sensing cellular stresses
title_sort sumoylation of the nuclear pore complex basket is involved in sensing cellular stresses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6467484/
https://www.ncbi.nlm.nih.gov/pubmed/30837289
http://dx.doi.org/10.1242/jcs.224279
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