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Binding of Carbonic Anhydrase IX to 45S rDNA Genes Is Prevented by Exportin-1 in Hypoxic Cells

Carbonic anhydrase IX (CA IX) is a surrogate marker of hypoxia, involved in survival and pH regulation in hypoxic cells. We have recently characterized its interactome, describing a set of proteins interacting with CA IX, mainly in hypoxic cells, including several members of the nucleocytoplasmic sh...

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Autores principales: Sasso, Emanuele, Vitale, Monica, Monteleone, Francesca, Boffo, Francesca Ludovica, Santoriello, Margherita, Sarnataro, Daniela, Garbi, Corrado, Sabatella, Mariangela, Crifò, Bianca, Paolella, Luca Alfredo, Minopoli, Giuseppina, Winum, Jean-Yves, Zambrano, Nicola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352447/
https://www.ncbi.nlm.nih.gov/pubmed/25793203
http://dx.doi.org/10.1155/2015/674920
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author Sasso, Emanuele
Vitale, Monica
Monteleone, Francesca
Boffo, Francesca Ludovica
Santoriello, Margherita
Sarnataro, Daniela
Garbi, Corrado
Sabatella, Mariangela
Crifò, Bianca
Paolella, Luca Alfredo
Minopoli, Giuseppina
Winum, Jean-Yves
Zambrano, Nicola
author_facet Sasso, Emanuele
Vitale, Monica
Monteleone, Francesca
Boffo, Francesca Ludovica
Santoriello, Margherita
Sarnataro, Daniela
Garbi, Corrado
Sabatella, Mariangela
Crifò, Bianca
Paolella, Luca Alfredo
Minopoli, Giuseppina
Winum, Jean-Yves
Zambrano, Nicola
author_sort Sasso, Emanuele
collection PubMed
description Carbonic anhydrase IX (CA IX) is a surrogate marker of hypoxia, involved in survival and pH regulation in hypoxic cells. We have recently characterized its interactome, describing a set of proteins interacting with CA IX, mainly in hypoxic cells, including several members of the nucleocytoplasmic shuttling apparatuses. Accordingly, we described complex subcellular localization for this enzyme in human cells, as well as the redistribution of a carbonic anhydrase IX pool to nucleoli during hypoxia. Starting from this evidence, we analyzed the possible contribution of carbonic anhydrase IX to transcription of the 45S rDNA genes, a process occurring in nucleoli. We highlighted the binding of carbonic anhydrase IX to nucleolar chromatin, which is regulated by oxygen levels. In fact, CA IX was found on 45S rDNA gene promoters in normoxic cells and less represented on these sites, in hypoxic cells and in cells subjected to acetazolamide-induced acidosis. Both conditions were associated with increased representation of carbonic anhydrase IX/exportin-1 complexes in nucleoli. 45S rRNA transcript levels were accordingly downrepresented. Inhibition of nuclear export by leptomycin B suggests a model in which exportin-1 acts as a decoy, in hypoxic cells, preventing carbonic anhydrase IX association with 45S rDNA gene promoters.
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spelling pubmed-43524472015-03-19 Binding of Carbonic Anhydrase IX to 45S rDNA Genes Is Prevented by Exportin-1 in Hypoxic Cells Sasso, Emanuele Vitale, Monica Monteleone, Francesca Boffo, Francesca Ludovica Santoriello, Margherita Sarnataro, Daniela Garbi, Corrado Sabatella, Mariangela Crifò, Bianca Paolella, Luca Alfredo Minopoli, Giuseppina Winum, Jean-Yves Zambrano, Nicola Biomed Res Int Research Article Carbonic anhydrase IX (CA IX) is a surrogate marker of hypoxia, involved in survival and pH regulation in hypoxic cells. We have recently characterized its interactome, describing a set of proteins interacting with CA IX, mainly in hypoxic cells, including several members of the nucleocytoplasmic shuttling apparatuses. Accordingly, we described complex subcellular localization for this enzyme in human cells, as well as the redistribution of a carbonic anhydrase IX pool to nucleoli during hypoxia. Starting from this evidence, we analyzed the possible contribution of carbonic anhydrase IX to transcription of the 45S rDNA genes, a process occurring in nucleoli. We highlighted the binding of carbonic anhydrase IX to nucleolar chromatin, which is regulated by oxygen levels. In fact, CA IX was found on 45S rDNA gene promoters in normoxic cells and less represented on these sites, in hypoxic cells and in cells subjected to acetazolamide-induced acidosis. Both conditions were associated with increased representation of carbonic anhydrase IX/exportin-1 complexes in nucleoli. 45S rRNA transcript levels were accordingly downrepresented. Inhibition of nuclear export by leptomycin B suggests a model in which exportin-1 acts as a decoy, in hypoxic cells, preventing carbonic anhydrase IX association with 45S rDNA gene promoters. Hindawi Publishing Corporation 2015 2015-02-22 /pmc/articles/PMC4352447/ /pubmed/25793203 http://dx.doi.org/10.1155/2015/674920 Text en Copyright © 2015 Emanuele Sasso et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sasso, Emanuele
Vitale, Monica
Monteleone, Francesca
Boffo, Francesca Ludovica
Santoriello, Margherita
Sarnataro, Daniela
Garbi, Corrado
Sabatella, Mariangela
Crifò, Bianca
Paolella, Luca Alfredo
Minopoli, Giuseppina
Winum, Jean-Yves
Zambrano, Nicola
Binding of Carbonic Anhydrase IX to 45S rDNA Genes Is Prevented by Exportin-1 in Hypoxic Cells
title Binding of Carbonic Anhydrase IX to 45S rDNA Genes Is Prevented by Exportin-1 in Hypoxic Cells
title_full Binding of Carbonic Anhydrase IX to 45S rDNA Genes Is Prevented by Exportin-1 in Hypoxic Cells
title_fullStr Binding of Carbonic Anhydrase IX to 45S rDNA Genes Is Prevented by Exportin-1 in Hypoxic Cells
title_full_unstemmed Binding of Carbonic Anhydrase IX to 45S rDNA Genes Is Prevented by Exportin-1 in Hypoxic Cells
title_short Binding of Carbonic Anhydrase IX to 45S rDNA Genes Is Prevented by Exportin-1 in Hypoxic Cells
title_sort binding of carbonic anhydrase ix to 45s rdna genes is prevented by exportin-1 in hypoxic cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352447/
https://www.ncbi.nlm.nih.gov/pubmed/25793203
http://dx.doi.org/10.1155/2015/674920
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