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Single-cell expression and Mendelian randomization analyses identify blood genes associated with lifespan and chronic diseases

The human lifespan is a heritable trait, which is intricately linked to the development of disorders. Here, we show that genetic associations for the parental lifespan are enriched in open chromatin of blood cells. By using blood expression quantitative trait loci (eQTL) derived from 31,684 samples,...

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Autores principales: Chignon, Arnaud, Bon-Baret, Valentin, Boulanger, Marie-Chloé, Li, Zhonglin, Argaud, Deborah, Bossé, Yohan, Thériault, Sébastien, Arsenault, Benoit J., Mathieu, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195437/
https://www.ncbi.nlm.nih.gov/pubmed/32358504
http://dx.doi.org/10.1038/s42003-020-0937-x
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author Chignon, Arnaud
Bon-Baret, Valentin
Boulanger, Marie-Chloé
Li, Zhonglin
Argaud, Deborah
Bossé, Yohan
Thériault, Sébastien
Arsenault, Benoit J.
Mathieu, Patrick
author_facet Chignon, Arnaud
Bon-Baret, Valentin
Boulanger, Marie-Chloé
Li, Zhonglin
Argaud, Deborah
Bossé, Yohan
Thériault, Sébastien
Arsenault, Benoit J.
Mathieu, Patrick
author_sort Chignon, Arnaud
collection PubMed
description The human lifespan is a heritable trait, which is intricately linked to the development of disorders. Here, we show that genetic associations for the parental lifespan are enriched in open chromatin of blood cells. By using blood expression quantitative trait loci (eQTL) derived from 31,684 samples, we identified for the lifespan 125 cis- and 559 trans-regulated expressed genes (eGenes) enriched in adaptive and innate responses. Analysis of blood single-cell expression data showed that eGenes were enriched in dendritic cells (DCs) and the modelling of cell ligand-receptor interactions predicted crosstalk between DCs and a cluster of monocytes with a signature of cytotoxicity. In two-sample Mendelian randomization (MR), we identified 16 blood cis-eGenes causally associated with the lifespan. In MR, the majority of cis-eGene-disorder association pairs had concordant effects with the lifespan. The present work underlined that the lifespan is linked with the immune response and identifies eGenes associated with the lifespan and disorders.
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spelling pubmed-71954372020-05-06 Single-cell expression and Mendelian randomization analyses identify blood genes associated with lifespan and chronic diseases Chignon, Arnaud Bon-Baret, Valentin Boulanger, Marie-Chloé Li, Zhonglin Argaud, Deborah Bossé, Yohan Thériault, Sébastien Arsenault, Benoit J. Mathieu, Patrick Commun Biol Article The human lifespan is a heritable trait, which is intricately linked to the development of disorders. Here, we show that genetic associations for the parental lifespan are enriched in open chromatin of blood cells. By using blood expression quantitative trait loci (eQTL) derived from 31,684 samples, we identified for the lifespan 125 cis- and 559 trans-regulated expressed genes (eGenes) enriched in adaptive and innate responses. Analysis of blood single-cell expression data showed that eGenes were enriched in dendritic cells (DCs) and the modelling of cell ligand-receptor interactions predicted crosstalk between DCs and a cluster of monocytes with a signature of cytotoxicity. In two-sample Mendelian randomization (MR), we identified 16 blood cis-eGenes causally associated with the lifespan. In MR, the majority of cis-eGene-disorder association pairs had concordant effects with the lifespan. The present work underlined that the lifespan is linked with the immune response and identifies eGenes associated with the lifespan and disorders. Nature Publishing Group UK 2020-05-01 /pmc/articles/PMC7195437/ /pubmed/32358504 http://dx.doi.org/10.1038/s42003-020-0937-x Text en © The Author(s) 2020 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
Chignon, Arnaud
Bon-Baret, Valentin
Boulanger, Marie-Chloé
Li, Zhonglin
Argaud, Deborah
Bossé, Yohan
Thériault, Sébastien
Arsenault, Benoit J.
Mathieu, Patrick
Single-cell expression and Mendelian randomization analyses identify blood genes associated with lifespan and chronic diseases
title Single-cell expression and Mendelian randomization analyses identify blood genes associated with lifespan and chronic diseases
title_full Single-cell expression and Mendelian randomization analyses identify blood genes associated with lifespan and chronic diseases
title_fullStr Single-cell expression and Mendelian randomization analyses identify blood genes associated with lifespan and chronic diseases
title_full_unstemmed Single-cell expression and Mendelian randomization analyses identify blood genes associated with lifespan and chronic diseases
title_short Single-cell expression and Mendelian randomization analyses identify blood genes associated with lifespan and chronic diseases
title_sort single-cell expression and mendelian randomization analyses identify blood genes associated with lifespan and chronic diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195437/
https://www.ncbi.nlm.nih.gov/pubmed/32358504
http://dx.doi.org/10.1038/s42003-020-0937-x
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