Epistatic interactions of genetic loci associated with age-related macular degeneration
Abstract The currently largest genome-wide association study (GWAS) for age-related macular degeneration (AMD) defines disease association with genome-wide significance for 52 independent common and rare genetic variants across 34 chromosomal loci. Overall, these loci contain over 7200 variants and...
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2021-06-01
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Online Access: | https://doi.org/10.1038/s41598-021-92351-4 |
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doaj-a4f2b1aa556848daa51932e3f871c3ac2021-06-27T11:31:42ZengNature Publishing GroupScientific Reports2045-23222021-06-0111111110.1038/s41598-021-92351-4Epistatic interactions of genetic loci associated with age-related macular degenerationChristina Kiel0Christoph A. Nebauer1Tobias Strunz2Simon Stelzl3Bernhard H. F. Weber4Institute of Human Genetics, University of RegensburgInstitute of Human Genetics, University of RegensburgInstitute of Human Genetics, University of RegensburgInstitute of Human Genetics, University of RegensburgInstitute of Human Genetics, University of RegensburgAbstract The currently largest genome-wide association study (GWAS) for age-related macular degeneration (AMD) defines disease association with genome-wide significance for 52 independent common and rare genetic variants across 34 chromosomal loci. Overall, these loci contain over 7200 variants and are enriched for genes with functions indicating several shared cellular processes. Still, the precise mechanisms leading to AMD pathology are largely unknown. Here, we exploit the phenomenon of epistatic interaction to identify seemingly independent AMD-associated variants that reveal joint effects on gene expression. We focus on genetic variants associated with lipid metabolism, organization of extracellular structures, and innate immunity, specifically the complement cascade. Multiple combinations of independent variants were used to generate genetic risk scores allowing gene expression in liver to be compared between low and high-risk AMD. We identified genetic variant combinations correlating significantly with expression of 26 genes, of which 19 have not been associated with AMD before. This study defines novel targets and allows prioritizing further functional work into AMD pathobiology.https://doi.org/10.1038/s41598-021-92351-4 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Christina Kiel Christoph A. Nebauer Tobias Strunz Simon Stelzl Bernhard H. F. Weber |
spellingShingle |
Christina Kiel Christoph A. Nebauer Tobias Strunz Simon Stelzl Bernhard H. F. Weber Epistatic interactions of genetic loci associated with age-related macular degeneration Scientific Reports |
author_facet |
Christina Kiel Christoph A. Nebauer Tobias Strunz Simon Stelzl Bernhard H. F. Weber |
author_sort |
Christina Kiel |
title |
Epistatic interactions of genetic loci associated with age-related macular degeneration |
title_short |
Epistatic interactions of genetic loci associated with age-related macular degeneration |
title_full |
Epistatic interactions of genetic loci associated with age-related macular degeneration |
title_fullStr |
Epistatic interactions of genetic loci associated with age-related macular degeneration |
title_full_unstemmed |
Epistatic interactions of genetic loci associated with age-related macular degeneration |
title_sort |
epistatic interactions of genetic loci associated with age-related macular degeneration |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-06-01 |
description |
Abstract The currently largest genome-wide association study (GWAS) for age-related macular degeneration (AMD) defines disease association with genome-wide significance for 52 independent common and rare genetic variants across 34 chromosomal loci. Overall, these loci contain over 7200 variants and are enriched for genes with functions indicating several shared cellular processes. Still, the precise mechanisms leading to AMD pathology are largely unknown. Here, we exploit the phenomenon of epistatic interaction to identify seemingly independent AMD-associated variants that reveal joint effects on gene expression. We focus on genetic variants associated with lipid metabolism, organization of extracellular structures, and innate immunity, specifically the complement cascade. Multiple combinations of independent variants were used to generate genetic risk scores allowing gene expression in liver to be compared between low and high-risk AMD. We identified genetic variant combinations correlating significantly with expression of 26 genes, of which 19 have not been associated with AMD before. This study defines novel targets and allows prioritizing further functional work into AMD pathobiology. |
url |
https://doi.org/10.1038/s41598-021-92351-4 |
work_keys_str_mv |
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