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Sequential Use of Transcriptional Profiling, Expression Quantitative Trait Mapping, and Gene Association Implicates MMP20 in Human Kidney Aging
Kidneys age at different rates, such that some people show little or no effects of aging whereas others show rapid functional decline. We sequentially used transcriptional profiling and expression quantitative trait loci (eQTL) mapping to narrow down which genes to test for association with kidney a...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752811/ https://www.ncbi.nlm.nih.gov/pubmed/19834535 http://dx.doi.org/10.1371/journal.pgen.1000685 |
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author | Wheeler, Heather E. Metter, E. Jeffrey Tanaka, Toshiko Absher, Devin Higgins, John Zahn, Jacob M. Wilhelmy, Julie Davis, Ronald W. Singleton, Andrew Myers, Richard M. Ferrucci, Luigi Kim, Stuart K. |
author_facet | Wheeler, Heather E. Metter, E. Jeffrey Tanaka, Toshiko Absher, Devin Higgins, John Zahn, Jacob M. Wilhelmy, Julie Davis, Ronald W. Singleton, Andrew Myers, Richard M. Ferrucci, Luigi Kim, Stuart K. |
author_sort | Wheeler, Heather E. |
collection | PubMed |
description | Kidneys age at different rates, such that some people show little or no effects of aging whereas others show rapid functional decline. We sequentially used transcriptional profiling and expression quantitative trait loci (eQTL) mapping to narrow down which genes to test for association with kidney aging. We first performed whole-genome transcriptional profiling to find 630 genes that change expression with age in the kidney. Using two methods to detect eQTLs, we found 101 of these age-regulated genes contain expression-associated SNPs. We tested the eQTLs for association with kidney aging, measured by glomerular filtration rate (GFR) using combined data from the Baltimore Longitudinal Study of Aging (BLSA) and the InCHIANTI study. We found a SNP association (rs1711437 in MMP20) with kidney aging (uncorrected p = 3.6×10(−5), empirical p = 0.01) that explains 1%–2% of the variance in GFR among individuals. The results of this sequential analysis may provide the first evidence for a gene association with kidney aging in humans. |
format | Text |
id | pubmed-2752811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-27528112009-10-16 Sequential Use of Transcriptional Profiling, Expression Quantitative Trait Mapping, and Gene Association Implicates MMP20 in Human Kidney Aging Wheeler, Heather E. Metter, E. Jeffrey Tanaka, Toshiko Absher, Devin Higgins, John Zahn, Jacob M. Wilhelmy, Julie Davis, Ronald W. Singleton, Andrew Myers, Richard M. Ferrucci, Luigi Kim, Stuart K. PLoS Genet Research Article Kidneys age at different rates, such that some people show little or no effects of aging whereas others show rapid functional decline. We sequentially used transcriptional profiling and expression quantitative trait loci (eQTL) mapping to narrow down which genes to test for association with kidney aging. We first performed whole-genome transcriptional profiling to find 630 genes that change expression with age in the kidney. Using two methods to detect eQTLs, we found 101 of these age-regulated genes contain expression-associated SNPs. We tested the eQTLs for association with kidney aging, measured by glomerular filtration rate (GFR) using combined data from the Baltimore Longitudinal Study of Aging (BLSA) and the InCHIANTI study. We found a SNP association (rs1711437 in MMP20) with kidney aging (uncorrected p = 3.6×10(−5), empirical p = 0.01) that explains 1%–2% of the variance in GFR among individuals. The results of this sequential analysis may provide the first evidence for a gene association with kidney aging in humans. Public Library of Science 2009-10-16 /pmc/articles/PMC2752811/ /pubmed/19834535 http://dx.doi.org/10.1371/journal.pgen.1000685 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Wheeler, Heather E. Metter, E. Jeffrey Tanaka, Toshiko Absher, Devin Higgins, John Zahn, Jacob M. Wilhelmy, Julie Davis, Ronald W. Singleton, Andrew Myers, Richard M. Ferrucci, Luigi Kim, Stuart K. Sequential Use of Transcriptional Profiling, Expression Quantitative Trait Mapping, and Gene Association Implicates MMP20 in Human Kidney Aging |
title | Sequential Use of Transcriptional Profiling, Expression Quantitative Trait Mapping, and Gene Association Implicates MMP20 in Human Kidney Aging |
title_full | Sequential Use of Transcriptional Profiling, Expression Quantitative Trait Mapping, and Gene Association Implicates MMP20 in Human Kidney Aging |
title_fullStr | Sequential Use of Transcriptional Profiling, Expression Quantitative Trait Mapping, and Gene Association Implicates MMP20 in Human Kidney Aging |
title_full_unstemmed | Sequential Use of Transcriptional Profiling, Expression Quantitative Trait Mapping, and Gene Association Implicates MMP20 in Human Kidney Aging |
title_short | Sequential Use of Transcriptional Profiling, Expression Quantitative Trait Mapping, and Gene Association Implicates MMP20 in Human Kidney Aging |
title_sort | sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates mmp20 in human kidney aging |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2752811/ https://www.ncbi.nlm.nih.gov/pubmed/19834535 http://dx.doi.org/10.1371/journal.pgen.1000685 |
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