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Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption
Coffee is one of the most consumed beverages world-wide and one of the primary sources of caffeine intake. Given its important health and economic impact, the underlying genetics of its consumption has been widely studied. Despite these efforts, much has still to be uncovered. In particular, the use...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997959/ https://www.ncbi.nlm.nih.gov/pubmed/27561104 http://dx.doi.org/10.1038/srep31590 |
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author | Pirastu, Nicola Kooyman, Maarten Robino, Antonietta van der Spek, Ashley Navarini, Luciano Amin, Najaf Karssen, Lennart C. Van Duijn, Cornelia M Gasparini, Paolo |
author_facet | Pirastu, Nicola Kooyman, Maarten Robino, Antonietta van der Spek, Ashley Navarini, Luciano Amin, Najaf Karssen, Lennart C. Van Duijn, Cornelia M Gasparini, Paolo |
author_sort | Pirastu, Nicola |
collection | PubMed |
description | Coffee is one of the most consumed beverages world-wide and one of the primary sources of caffeine intake. Given its important health and economic impact, the underlying genetics of its consumption has been widely studied. Despite these efforts, much has still to be uncovered. In particular, the use of non-additive genetic models may uncover new information about the genetic variants driving coffee consumption. We have conducted a genome-wide association study in two Italian populations using additive, recessive and dominant models for analysis. This has uncovered a significant association in the PDSS2 gene under the recessive model that has been replicated in an independent cohort from the Netherlands (ERF). The identified gene has been shown to negatively regulate the expression of the caffeine metabolism genes and can thus be linked to coffee consumption. Further bioinformatics analysis of eQTL and histone marks from Roadmap data has evidenced a possible role of the identified SNPs in regulating PDSS2 gene expression through enhancers present in its intron. Our results highlight a novel gene which regulates coffee consumption by regulating the expression of the genes linked to caffeine metabolism. Further studies will be needed to clarify the biological mechanism which links PDSS2 and coffee consumption. |
format | Online Article Text |
id | pubmed-4997959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49979592016-09-01 Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption Pirastu, Nicola Kooyman, Maarten Robino, Antonietta van der Spek, Ashley Navarini, Luciano Amin, Najaf Karssen, Lennart C. Van Duijn, Cornelia M Gasparini, Paolo Sci Rep Article Coffee is one of the most consumed beverages world-wide and one of the primary sources of caffeine intake. Given its important health and economic impact, the underlying genetics of its consumption has been widely studied. Despite these efforts, much has still to be uncovered. In particular, the use of non-additive genetic models may uncover new information about the genetic variants driving coffee consumption. We have conducted a genome-wide association study in two Italian populations using additive, recessive and dominant models for analysis. This has uncovered a significant association in the PDSS2 gene under the recessive model that has been replicated in an independent cohort from the Netherlands (ERF). The identified gene has been shown to negatively regulate the expression of the caffeine metabolism genes and can thus be linked to coffee consumption. Further bioinformatics analysis of eQTL and histone marks from Roadmap data has evidenced a possible role of the identified SNPs in regulating PDSS2 gene expression through enhancers present in its intron. Our results highlight a novel gene which regulates coffee consumption by regulating the expression of the genes linked to caffeine metabolism. Further studies will be needed to clarify the biological mechanism which links PDSS2 and coffee consumption. Nature Publishing Group 2016-08-25 /pmc/articles/PMC4997959/ /pubmed/27561104 http://dx.doi.org/10.1038/srep31590 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Pirastu, Nicola Kooyman, Maarten Robino, Antonietta van der Spek, Ashley Navarini, Luciano Amin, Najaf Karssen, Lennart C. Van Duijn, Cornelia M Gasparini, Paolo Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption |
title | Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption |
title_full | Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption |
title_fullStr | Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption |
title_full_unstemmed | Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption |
title_short | Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption |
title_sort | non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997959/ https://www.ncbi.nlm.nih.gov/pubmed/27561104 http://dx.doi.org/10.1038/srep31590 |
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