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Identification of Genes Promoting Skin Youthfulness by Genome-Wide Association Study
To identify genes that promote facial skin youthfulness (SY), a genome-wide association study on an Ashkenazi Jewish discovery group (n=428) was performed using Affymetrix 6.0 Single-Nucleotide Polymorphism (SNP) Array. After SNP quality controls, 901,470 SNPs remained for analysis. The eigenstrat m...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923276/ https://www.ncbi.nlm.nih.gov/pubmed/24037343 http://dx.doi.org/10.1038/jid.2013.381 |
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author | Chang, Anne L.S. Atzmon, Gil Bergman, Aviv Brugmann, Samantha Atwood, Scott X Chang, Howard Y Barzilai, Nir |
author_facet | Chang, Anne L.S. Atzmon, Gil Bergman, Aviv Brugmann, Samantha Atwood, Scott X Chang, Howard Y Barzilai, Nir |
author_sort | Chang, Anne L.S. |
collection | PubMed |
description | To identify genes that promote facial skin youthfulness (SY), a genome-wide association study on an Ashkenazi Jewish discovery group (n=428) was performed using Affymetrix 6.0 Single-Nucleotide Polymorphism (SNP) Array. After SNP quality controls, 901,470 SNPs remained for analysis. The eigenstrat method showed no stratification. Cases and controls were identified by global facial skin aging severity including intrinsic and extrinsic parameters. Linear regression adjusted for age and gender, with no significant differences in smoking history, body mass index, menopausal status, or personal or family history of centenarians. Six SNPs met the Bonferroni threshold with P(allele)<10(−8); two of these six had P(genotype)<10(−8). Quantitative trait loci mapping confirmed linkage disequilibrium. The six SNPs were interrogated by MassARRAY in a replication group (n=436) with confirmation of rs6975107, an intronic region of KCND2 (potassium voltage-gated channel, Shal-related family member 2) (P(genotype)=0.023). A second replication group (n=371) confirmed rs318125, downstream of DIAPH2 (diaphanous homolog 2 (Drosophila)) (P(allele)=0.010, P(genotype)=0.002) and rs7616661, downstream of EDEM1 (ER degradation enhancer, mannosidase α-like 1) (P(genotype)=0.042). DIAPH2 has been associated with premature ovarian insufficiency, an aging phenotype in humans. EDEM1 associates with lifespan in animal models, although not humans. KCND2 is expressed in human skin, but has not been associated with aging. These genes represent new candidate genes to study the molecular basis of healthy skin aging. |
format | Online Article Text |
id | pubmed-3923276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-39232762014-02-13 Identification of Genes Promoting Skin Youthfulness by Genome-Wide Association Study Chang, Anne L.S. Atzmon, Gil Bergman, Aviv Brugmann, Samantha Atwood, Scott X Chang, Howard Y Barzilai, Nir J Invest Dermatol Original Article To identify genes that promote facial skin youthfulness (SY), a genome-wide association study on an Ashkenazi Jewish discovery group (n=428) was performed using Affymetrix 6.0 Single-Nucleotide Polymorphism (SNP) Array. After SNP quality controls, 901,470 SNPs remained for analysis. The eigenstrat method showed no stratification. Cases and controls were identified by global facial skin aging severity including intrinsic and extrinsic parameters. Linear regression adjusted for age and gender, with no significant differences in smoking history, body mass index, menopausal status, or personal or family history of centenarians. Six SNPs met the Bonferroni threshold with P(allele)<10(−8); two of these six had P(genotype)<10(−8). Quantitative trait loci mapping confirmed linkage disequilibrium. The six SNPs were interrogated by MassARRAY in a replication group (n=436) with confirmation of rs6975107, an intronic region of KCND2 (potassium voltage-gated channel, Shal-related family member 2) (P(genotype)=0.023). A second replication group (n=371) confirmed rs318125, downstream of DIAPH2 (diaphanous homolog 2 (Drosophila)) (P(allele)=0.010, P(genotype)=0.002) and rs7616661, downstream of EDEM1 (ER degradation enhancer, mannosidase α-like 1) (P(genotype)=0.042). DIAPH2 has been associated with premature ovarian insufficiency, an aging phenotype in humans. EDEM1 associates with lifespan in animal models, although not humans. KCND2 is expressed in human skin, but has not been associated with aging. These genes represent new candidate genes to study the molecular basis of healthy skin aging. Nature Publishing Group 2014-03 2013-10-17 /pmc/articles/PMC3923276/ /pubmed/24037343 http://dx.doi.org/10.1038/jid.2013.381 Text en Copyright © 2014 The Society for Investigative Dermatology, Inc http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Chang, Anne L.S. Atzmon, Gil Bergman, Aviv Brugmann, Samantha Atwood, Scott X Chang, Howard Y Barzilai, Nir Identification of Genes Promoting Skin Youthfulness by Genome-Wide Association Study |
title | Identification of Genes Promoting Skin Youthfulness by Genome-Wide Association Study |
title_full | Identification of Genes Promoting Skin Youthfulness by Genome-Wide Association Study |
title_fullStr | Identification of Genes Promoting Skin Youthfulness by Genome-Wide Association Study |
title_full_unstemmed | Identification of Genes Promoting Skin Youthfulness by Genome-Wide Association Study |
title_short | Identification of Genes Promoting Skin Youthfulness by Genome-Wide Association Study |
title_sort | identification of genes promoting skin youthfulness by genome-wide association study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923276/ https://www.ncbi.nlm.nih.gov/pubmed/24037343 http://dx.doi.org/10.1038/jid.2013.381 |
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