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Accessing Data Resources in the Mouse Phenome Database for Genetic Analysis of Murine Life Span and Health Span

Understanding the source of genetic variation in aging and using this variation to define the molecular mechanisms of healthy aging require deep and broad quantification of a host of physiological, morphological, and behavioral endpoints. The murine model is a powerful system in which to understand...

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Autores principales: Bogue, Molly A., Peters, Luanne L., Paigen, Beverly, Korstanje, Ron, Yuan, Rong, Ackert-Bicknell, Cheryl, Grubb, Stephen C., Churchill, Gary A., Chesler, Elissa J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707687/
https://www.ncbi.nlm.nih.gov/pubmed/25533306
http://dx.doi.org/10.1093/gerona/glu223
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author Bogue, Molly A.
Peters, Luanne L.
Paigen, Beverly
Korstanje, Ron
Yuan, Rong
Ackert-Bicknell, Cheryl
Grubb, Stephen C.
Churchill, Gary A.
Chesler, Elissa J.
author_facet Bogue, Molly A.
Peters, Luanne L.
Paigen, Beverly
Korstanje, Ron
Yuan, Rong
Ackert-Bicknell, Cheryl
Grubb, Stephen C.
Churchill, Gary A.
Chesler, Elissa J.
author_sort Bogue, Molly A.
collection PubMed
description Understanding the source of genetic variation in aging and using this variation to define the molecular mechanisms of healthy aging require deep and broad quantification of a host of physiological, morphological, and behavioral endpoints. The murine model is a powerful system in which to understand the relations across age-related phenotypes and to identify research models with variation in life span and health span. The Jackson Laboratory Nathan Shock Center of Excellence in the Basic Biology of Aging has performed broad characterization of aging in genetically diverse laboratory mice and has placed these data, along with data from several other major aging initiatives, into the interactive Mouse Phenome Database. The data may be accessed and analyzed by researchers interested in finding mouse models for specific aging processes, age-related health and disease states, and for genetic analysis of aging variation and trait covariation. We expect that by placing these data in the hands of the aging community that there will be (a) accelerated genetic analyses of aging processes, (b) discovery of genetic loci regulating life span, (c) identification of compelling correlations between life span and susceptibility for age-related disorders, and (d) discovery of concordant genomic loci influencing life span and aging phenotypes between mouse and humans.
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spelling pubmed-47076872016-01-12 Accessing Data Resources in the Mouse Phenome Database for Genetic Analysis of Murine Life Span and Health Span Bogue, Molly A. Peters, Luanne L. Paigen, Beverly Korstanje, Ron Yuan, Rong Ackert-Bicknell, Cheryl Grubb, Stephen C. Churchill, Gary A. Chesler, Elissa J. J Gerontol A Biol Sci Med Sci Original Article Understanding the source of genetic variation in aging and using this variation to define the molecular mechanisms of healthy aging require deep and broad quantification of a host of physiological, morphological, and behavioral endpoints. The murine model is a powerful system in which to understand the relations across age-related phenotypes and to identify research models with variation in life span and health span. The Jackson Laboratory Nathan Shock Center of Excellence in the Basic Biology of Aging has performed broad characterization of aging in genetically diverse laboratory mice and has placed these data, along with data from several other major aging initiatives, into the interactive Mouse Phenome Database. The data may be accessed and analyzed by researchers interested in finding mouse models for specific aging processes, age-related health and disease states, and for genetic analysis of aging variation and trait covariation. We expect that by placing these data in the hands of the aging community that there will be (a) accelerated genetic analyses of aging processes, (b) discovery of genetic loci regulating life span, (c) identification of compelling correlations between life span and susceptibility for age-related disorders, and (d) discovery of concordant genomic loci influencing life span and aging phenotypes between mouse and humans. Oxford University Press 2016-02 2014-12-22 /pmc/articles/PMC4707687/ /pubmed/25533306 http://dx.doi.org/10.1093/gerona/glu223 Text en © The Author 2014. Published by Oxford University Press on behalf of The Gerontological Society of America. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Bogue, Molly A.
Peters, Luanne L.
Paigen, Beverly
Korstanje, Ron
Yuan, Rong
Ackert-Bicknell, Cheryl
Grubb, Stephen C.
Churchill, Gary A.
Chesler, Elissa J.
Accessing Data Resources in the Mouse Phenome Database for Genetic Analysis of Murine Life Span and Health Span
title Accessing Data Resources in the Mouse Phenome Database for Genetic Analysis of Murine Life Span and Health Span
title_full Accessing Data Resources in the Mouse Phenome Database for Genetic Analysis of Murine Life Span and Health Span
title_fullStr Accessing Data Resources in the Mouse Phenome Database for Genetic Analysis of Murine Life Span and Health Span
title_full_unstemmed Accessing Data Resources in the Mouse Phenome Database for Genetic Analysis of Murine Life Span and Health Span
title_short Accessing Data Resources in the Mouse Phenome Database for Genetic Analysis of Murine Life Span and Health Span
title_sort accessing data resources in the mouse phenome database for genetic analysis of murine life span and health span
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707687/
https://www.ncbi.nlm.nih.gov/pubmed/25533306
http://dx.doi.org/10.1093/gerona/glu223
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