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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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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. |
format | Online Article Text |
id | pubmed-4352447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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