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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,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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. |
format | Online Article Text |
id | pubmed-7195437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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