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An allelic variant in the intergenic region between ERAP1 and ERAP2 correlates with an inverse expression of the two genes

The Endoplasmatic Reticulum Aminopeptidases ERAP1 and ERAP2 are implicated in a variety of immune and non-immune functions. Most studies however have focused on their role in shaping the HLA class I peptidome by trimming peptides to the optimal size. Genome Wide Association Studies highlighted non-s...

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Autores principales: Paladini, Fabiana, Fiorillo, Maria Teresa, Vitulano, Carolina, Tedeschi, Valentina, Piga, Matteo, Cauli, Alberto, Mathieu, Alessandro, Sorrentino, Rosa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039459/
https://www.ncbi.nlm.nih.gov/pubmed/29991817
http://dx.doi.org/10.1038/s41598-018-28799-8
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author Paladini, Fabiana
Fiorillo, Maria Teresa
Vitulano, Carolina
Tedeschi, Valentina
Piga, Matteo
Cauli, Alberto
Mathieu, Alessandro
Sorrentino, Rosa
author_facet Paladini, Fabiana
Fiorillo, Maria Teresa
Vitulano, Carolina
Tedeschi, Valentina
Piga, Matteo
Cauli, Alberto
Mathieu, Alessandro
Sorrentino, Rosa
author_sort Paladini, Fabiana
collection PubMed
description The Endoplasmatic Reticulum Aminopeptidases ERAP1 and ERAP2 are implicated in a variety of immune and non-immune functions. Most studies however have focused on their role in shaping the HLA class I peptidome by trimming peptides to the optimal size. Genome Wide Association Studies highlighted non-synonymous polymorphisms in their coding regions as associated with several immune mediated diseases. The two genes lie contiguous and oppositely oriented on the 5q15 chromosomal region. Very little is known about the transcriptional regulation and the quantitative variations of these enzymes. Here, we correlated the level of transcripts and proteins of the two aminopeptidases in B-lymphoblastoid cell lines from 44 donors harbouring allelic variants in the intergenic region between ERAP1 and ERAP2. We found that the presence of a G instead of an A at SNP rs75862629 in the ERAP2 gene promoter strongly influences the expression of the two ERAPs with a down-modulation of ERAP2 coupled with a significant higher expression of ERAP1. We therefore show here for the first time a coordinated quantitative regulation of the two ERAP genes, which can be relevant for the setting of specific therapeutic approaches.
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spelling pubmed-60394592018-07-12 An allelic variant in the intergenic region between ERAP1 and ERAP2 correlates with an inverse expression of the two genes Paladini, Fabiana Fiorillo, Maria Teresa Vitulano, Carolina Tedeschi, Valentina Piga, Matteo Cauli, Alberto Mathieu, Alessandro Sorrentino, Rosa Sci Rep Article The Endoplasmatic Reticulum Aminopeptidases ERAP1 and ERAP2 are implicated in a variety of immune and non-immune functions. Most studies however have focused on their role in shaping the HLA class I peptidome by trimming peptides to the optimal size. Genome Wide Association Studies highlighted non-synonymous polymorphisms in their coding regions as associated with several immune mediated diseases. The two genes lie contiguous and oppositely oriented on the 5q15 chromosomal region. Very little is known about the transcriptional regulation and the quantitative variations of these enzymes. Here, we correlated the level of transcripts and proteins of the two aminopeptidases in B-lymphoblastoid cell lines from 44 donors harbouring allelic variants in the intergenic region between ERAP1 and ERAP2. We found that the presence of a G instead of an A at SNP rs75862629 in the ERAP2 gene promoter strongly influences the expression of the two ERAPs with a down-modulation of ERAP2 coupled with a significant higher expression of ERAP1. We therefore show here for the first time a coordinated quantitative regulation of the two ERAP genes, which can be relevant for the setting of specific therapeutic approaches. Nature Publishing Group UK 2018-07-10 /pmc/articles/PMC6039459/ /pubmed/29991817 http://dx.doi.org/10.1038/s41598-018-28799-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Paladini, Fabiana
Fiorillo, Maria Teresa
Vitulano, Carolina
Tedeschi, Valentina
Piga, Matteo
Cauli, Alberto
Mathieu, Alessandro
Sorrentino, Rosa
An allelic variant in the intergenic region between ERAP1 and ERAP2 correlates with an inverse expression of the two genes
title An allelic variant in the intergenic region between ERAP1 and ERAP2 correlates with an inverse expression of the two genes
title_full An allelic variant in the intergenic region between ERAP1 and ERAP2 correlates with an inverse expression of the two genes
title_fullStr An allelic variant in the intergenic region between ERAP1 and ERAP2 correlates with an inverse expression of the two genes
title_full_unstemmed An allelic variant in the intergenic region between ERAP1 and ERAP2 correlates with an inverse expression of the two genes
title_short An allelic variant in the intergenic region between ERAP1 and ERAP2 correlates with an inverse expression of the two genes
title_sort allelic variant in the intergenic region between erap1 and erap2 correlates with an inverse expression of the two genes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6039459/
https://www.ncbi.nlm.nih.gov/pubmed/29991817
http://dx.doi.org/10.1038/s41598-018-28799-8
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