Cargando…
Genomic modulators of gene expression in human neutrophils
Neutrophils form the most abundant leukocyte subset and are central to many disease processes. Technical challenges in transcriptomic profiling have prohibited genomic approaches to date. Here we map expression quantitative trait loci (eQTL) in peripheral blood CD16+ neutrophils from 101 healthy Eur...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507005/ https://www.ncbi.nlm.nih.gov/pubmed/26151758 http://dx.doi.org/10.1038/ncomms8545 |
_version_ | 1782381757476110336 |
---|---|
author | Naranbhai, Vivek Fairfax, Benjamin P. Makino, Seiko Humburg, Peter Wong, Daniel Ng, Esther Hill, Adrian V. S. Knight, Julian C. |
author_facet | Naranbhai, Vivek Fairfax, Benjamin P. Makino, Seiko Humburg, Peter Wong, Daniel Ng, Esther Hill, Adrian V. S. Knight, Julian C. |
author_sort | Naranbhai, Vivek |
collection | PubMed |
description | Neutrophils form the most abundant leukocyte subset and are central to many disease processes. Technical challenges in transcriptomic profiling have prohibited genomic approaches to date. Here we map expression quantitative trait loci (eQTL) in peripheral blood CD16+ neutrophils from 101 healthy European adults. We identify cis-eQTL for 3281 neutrophil-expressed genes including many implicated in neutrophil function, with 450 of these not previously observed in myeloid or lymphoid cells. Paired comparison with monocyte eQTL demonstrates nuanced conditioning of genetic regulation of gene expression by cellular context, which relates to cell-type-specific DNA methylation and histone modifications. Neutrophil eQTL are markedly enriched for trait-associated variants particularly autoimmune, allergy and infectious disease. We further demonstrate how eQTL in PADI4 and NOD2 delineate risk variant function in rheumatoid arthritis, leprosy and Crohn’s disease. Taken together, these data help advance understanding of the genetics of gene expression, neutrophil biology and immune-related diseases. |
format | Online Article Text |
id | pubmed-4507005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45070052015-07-21 Genomic modulators of gene expression in human neutrophils Naranbhai, Vivek Fairfax, Benjamin P. Makino, Seiko Humburg, Peter Wong, Daniel Ng, Esther Hill, Adrian V. S. Knight, Julian C. Nat Commun Article Neutrophils form the most abundant leukocyte subset and are central to many disease processes. Technical challenges in transcriptomic profiling have prohibited genomic approaches to date. Here we map expression quantitative trait loci (eQTL) in peripheral blood CD16+ neutrophils from 101 healthy European adults. We identify cis-eQTL for 3281 neutrophil-expressed genes including many implicated in neutrophil function, with 450 of these not previously observed in myeloid or lymphoid cells. Paired comparison with monocyte eQTL demonstrates nuanced conditioning of genetic regulation of gene expression by cellular context, which relates to cell-type-specific DNA methylation and histone modifications. Neutrophil eQTL are markedly enriched for trait-associated variants particularly autoimmune, allergy and infectious disease. We further demonstrate how eQTL in PADI4 and NOD2 delineate risk variant function in rheumatoid arthritis, leprosy and Crohn’s disease. Taken together, these data help advance understanding of the genetics of gene expression, neutrophil biology and immune-related diseases. Nature Publishing Group 2015-07-07 /pmc/articles/PMC4507005/ /pubmed/26151758 http://dx.doi.org/10.1038/ncomms8545 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. https://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/ (https://creativecommons.org/licenses/by/4.0/) |
spellingShingle | Article Naranbhai, Vivek Fairfax, Benjamin P. Makino, Seiko Humburg, Peter Wong, Daniel Ng, Esther Hill, Adrian V. S. Knight, Julian C. Genomic modulators of gene expression in human neutrophils |
title | Genomic modulators of gene expression in human neutrophils |
title_full | Genomic modulators of gene expression in human neutrophils |
title_fullStr | Genomic modulators of gene expression in human neutrophils |
title_full_unstemmed | Genomic modulators of gene expression in human neutrophils |
title_short | Genomic modulators of gene expression in human neutrophils |
title_sort | genomic modulators of gene expression in human neutrophils |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507005/ https://www.ncbi.nlm.nih.gov/pubmed/26151758 http://dx.doi.org/10.1038/ncomms8545 |
work_keys_str_mv | AT naranbhaivivek genomicmodulatorsofgeneexpressioninhumanneutrophils AT fairfaxbenjaminp genomicmodulatorsofgeneexpressioninhumanneutrophils AT makinoseiko genomicmodulatorsofgeneexpressioninhumanneutrophils AT humburgpeter genomicmodulatorsofgeneexpressioninhumanneutrophils AT wongdaniel genomicmodulatorsofgeneexpressioninhumanneutrophils AT ngesther genomicmodulatorsofgeneexpressioninhumanneutrophils AT hilladrianvs genomicmodulatorsofgeneexpressioninhumanneutrophils AT knightjulianc genomicmodulatorsofgeneexpressioninhumanneutrophils |