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Mitochondrial localization of the OAS1 p46 isoform associated with a common single nucleotide polymorphism

BACKGROUND: The expression of 2′-5′-Oligoadenylate synthetases (OASs) is induced by type 1 Interferons (IFNs) in response to viral infection. The OAS proteins have a unique ability to produce 2′-5′ Oligoadenylates, which bind and activate the ribonuclease RNase L. The RNase L degrades cellular RNAs...

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Autores principales: Kjær, Karina Hansen, Pahus, Jytte, Hansen, Mariann Fagernæs, Poulsen, Jesper Buchhave, Christensen, Erik Ilsø, Justesen, Just, Martensen, Pia Møller
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165621/
https://www.ncbi.nlm.nih.gov/pubmed/25205466
http://dx.doi.org/10.1186/1471-2121-15-33
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author Kjær, Karina Hansen
Pahus, Jytte
Hansen, Mariann Fagernæs
Poulsen, Jesper Buchhave
Christensen, Erik Ilsø
Justesen, Just
Martensen, Pia Møller
author_facet Kjær, Karina Hansen
Pahus, Jytte
Hansen, Mariann Fagernæs
Poulsen, Jesper Buchhave
Christensen, Erik Ilsø
Justesen, Just
Martensen, Pia Møller
author_sort Kjær, Karina Hansen
collection PubMed
description BACKGROUND: The expression of 2′-5′-Oligoadenylate synthetases (OASs) is induced by type 1 Interferons (IFNs) in response to viral infection. The OAS proteins have a unique ability to produce 2′-5′ Oligoadenylates, which bind and activate the ribonuclease RNase L. The RNase L degrades cellular RNAs which in turn inhibits protein translation and induces apoptosis. Several single nucleotide polymorphisms (SNPs) in the OAS1 gene have been associated with disease. We have investigated the functional effect of two common SNPs in the OAS1 gene. The SNP rs10774671 affects splicing to one of the exons in the OAS1 gene giving rise to differential expression of the OAS1 isoforms, and the SNP rs1131454 (former rs3741981) resides in exon 3 giving rise to OAS1 isoforms with either a Glycine or a Serine at position 162 in the core OAS unit. RESULTS: We have used three human cell lines with different genotypes in the OAS1 SNP rs10774671, HeLa cells with the AA genotype, HT1080 cells with AG, and Daudi cells with GG. The main OAS1 isoform expressed in Daudi and HT1080 cells was p46, and the main OAS1 isoform expressed in HeLa cells was p42. In addition, low levels of the OAS1 p52 mRNA was detected in HeLa cells and p48 mRNA in Daudi cells, and trace amounts of p44a mRNA were detected in the three cell lines treated with type 1 interferon. We show that the OAS1 p46 isoform was localized in the mitochondria in Daudi cells, whereas the OAS1 isoforms in HeLa cells were primarily localized in cytoplasmic vacuoles/lysosomes. By using recombinantly expressed OAS1 mutant proteins, we found that the OAS1 SNP rs1131454 (former rs3741981) did not affect the enzymatic OAS1 activity. CONCLUSIONS: The SNP rs10774671 determines differential expression of the OAS1 isoforms. In Daudi and HT1080 cells the p46 isoform is the most abundantly expressed isoform associated with the G allele, whereas in HeLa cells the most abundantly expressed isoform is p42 associated with the A allele. The SNP rs1131454 (former rs3741981) does not interfere with OAS1 enzyme activity. The OAS1 p46 isoform localizes to the mitochondria, therefore a full 2-5A system can now be found in the mitochondria.
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spelling pubmed-41656212014-09-17 Mitochondrial localization of the OAS1 p46 isoform associated with a common single nucleotide polymorphism Kjær, Karina Hansen Pahus, Jytte Hansen, Mariann Fagernæs Poulsen, Jesper Buchhave Christensen, Erik Ilsø Justesen, Just Martensen, Pia Møller BMC Cell Biol Research Article BACKGROUND: The expression of 2′-5′-Oligoadenylate synthetases (OASs) is induced by type 1 Interferons (IFNs) in response to viral infection. The OAS proteins have a unique ability to produce 2′-5′ Oligoadenylates, which bind and activate the ribonuclease RNase L. The RNase L degrades cellular RNAs which in turn inhibits protein translation and induces apoptosis. Several single nucleotide polymorphisms (SNPs) in the OAS1 gene have been associated with disease. We have investigated the functional effect of two common SNPs in the OAS1 gene. The SNP rs10774671 affects splicing to one of the exons in the OAS1 gene giving rise to differential expression of the OAS1 isoforms, and the SNP rs1131454 (former rs3741981) resides in exon 3 giving rise to OAS1 isoforms with either a Glycine or a Serine at position 162 in the core OAS unit. RESULTS: We have used three human cell lines with different genotypes in the OAS1 SNP rs10774671, HeLa cells with the AA genotype, HT1080 cells with AG, and Daudi cells with GG. The main OAS1 isoform expressed in Daudi and HT1080 cells was p46, and the main OAS1 isoform expressed in HeLa cells was p42. In addition, low levels of the OAS1 p52 mRNA was detected in HeLa cells and p48 mRNA in Daudi cells, and trace amounts of p44a mRNA were detected in the three cell lines treated with type 1 interferon. We show that the OAS1 p46 isoform was localized in the mitochondria in Daudi cells, whereas the OAS1 isoforms in HeLa cells were primarily localized in cytoplasmic vacuoles/lysosomes. By using recombinantly expressed OAS1 mutant proteins, we found that the OAS1 SNP rs1131454 (former rs3741981) did not affect the enzymatic OAS1 activity. CONCLUSIONS: The SNP rs10774671 determines differential expression of the OAS1 isoforms. In Daudi and HT1080 cells the p46 isoform is the most abundantly expressed isoform associated with the G allele, whereas in HeLa cells the most abundantly expressed isoform is p42 associated with the A allele. The SNP rs1131454 (former rs3741981) does not interfere with OAS1 enzyme activity. The OAS1 p46 isoform localizes to the mitochondria, therefore a full 2-5A system can now be found in the mitochondria. BioMed Central 2014-09-09 /pmc/articles/PMC4165621/ /pubmed/25205466 http://dx.doi.org/10.1186/1471-2121-15-33 Text en Copyright © 2014 Kjær et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This 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 the original work is properly credited. 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
Kjær, Karina Hansen
Pahus, Jytte
Hansen, Mariann Fagernæs
Poulsen, Jesper Buchhave
Christensen, Erik Ilsø
Justesen, Just
Martensen, Pia Møller
Mitochondrial localization of the OAS1 p46 isoform associated with a common single nucleotide polymorphism
title Mitochondrial localization of the OAS1 p46 isoform associated with a common single nucleotide polymorphism
title_full Mitochondrial localization of the OAS1 p46 isoform associated with a common single nucleotide polymorphism
title_fullStr Mitochondrial localization of the OAS1 p46 isoform associated with a common single nucleotide polymorphism
title_full_unstemmed Mitochondrial localization of the OAS1 p46 isoform associated with a common single nucleotide polymorphism
title_short Mitochondrial localization of the OAS1 p46 isoform associated with a common single nucleotide polymorphism
title_sort mitochondrial localization of the oas1 p46 isoform associated with a common single nucleotide polymorphism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165621/
https://www.ncbi.nlm.nih.gov/pubmed/25205466
http://dx.doi.org/10.1186/1471-2121-15-33
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