Cargando…
AGEMAP: A Gene Expression Database for Aging in Mice
We present the AGEMAP (Atlas of Gene Expression in Mouse Aging Project) gene expression database, which is a resource that catalogs changes in gene expression as a function of age in mice. The AGEMAP database includes expression changes for 8,932 genes in 16 tissues as a function of age. We found gr...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2098796/ https://www.ncbi.nlm.nih.gov/pubmed/18081424 http://dx.doi.org/10.1371/journal.pgen.0030201 |
_version_ | 1782138278732890112 |
---|---|
author | Zahn, Jacob M Poosala, Suresh Owen, Art B Ingram, Donald K Lustig, Ana Carter, Arnell Weeraratna, Ashani T Taub, Dennis D Gorospe, Myriam Mazan-Mamczarz, Krystyna Lakatta, Edward G Boheler, Kenneth R Xu, Xiangru Mattson, Mark P Falco, Geppino Ko, Minoru S. H Schlessinger, David Firman, Jeffrey Kummerfeld, Sarah K Wood, William H Zonderman, Alan B Kim, Stuart K Becker, Kevin G |
author_facet | Zahn, Jacob M Poosala, Suresh Owen, Art B Ingram, Donald K Lustig, Ana Carter, Arnell Weeraratna, Ashani T Taub, Dennis D Gorospe, Myriam Mazan-Mamczarz, Krystyna Lakatta, Edward G Boheler, Kenneth R Xu, Xiangru Mattson, Mark P Falco, Geppino Ko, Minoru S. H Schlessinger, David Firman, Jeffrey Kummerfeld, Sarah K Wood, William H Zonderman, Alan B Kim, Stuart K Becker, Kevin G |
author_sort | Zahn, Jacob M |
collection | PubMed |
description | We present the AGEMAP (Atlas of Gene Expression in Mouse Aging Project) gene expression database, which is a resource that catalogs changes in gene expression as a function of age in mice. The AGEMAP database includes expression changes for 8,932 genes in 16 tissues as a function of age. We found great heterogeneity in the amount of transcriptional changes with age in different tissues. Some tissues displayed large transcriptional differences in old mice, suggesting that these tissues may contribute strongly to organismal decline. Other tissues showed few or no changes in expression with age, indicating strong levels of homeostasis throughout life. Based on the pattern of age-related transcriptional changes, we found that tissues could be classified into one of three aging processes: (1) a pattern common to neural tissues, (2) a pattern for vascular tissues, and (3) a pattern for steroid-responsive tissues. We observed that different tissues age in a coordinated fashion in individual mice, such that certain mice exhibit rapid aging, whereas others exhibit slow aging for multiple tissues. Finally, we compared the transcriptional profiles for aging in mice to those from humans, flies, and worms. We found that genes involved in the electron transport chain show common age regulation in all four species, indicating that these genes may be exceptionally good markers of aging. However, we saw no overall correlation of age regulation between mice and humans, suggesting that aging processes in mice and humans may be fundamentally different. |
format | Text |
id | pubmed-2098796 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-20987962007-11-29 AGEMAP: A Gene Expression Database for Aging in Mice Zahn, Jacob M Poosala, Suresh Owen, Art B Ingram, Donald K Lustig, Ana Carter, Arnell Weeraratna, Ashani T Taub, Dennis D Gorospe, Myriam Mazan-Mamczarz, Krystyna Lakatta, Edward G Boheler, Kenneth R Xu, Xiangru Mattson, Mark P Falco, Geppino Ko, Minoru S. H Schlessinger, David Firman, Jeffrey Kummerfeld, Sarah K Wood, William H Zonderman, Alan B Kim, Stuart K Becker, Kevin G PLoS Genet Research Article We present the AGEMAP (Atlas of Gene Expression in Mouse Aging Project) gene expression database, which is a resource that catalogs changes in gene expression as a function of age in mice. The AGEMAP database includes expression changes for 8,932 genes in 16 tissues as a function of age. We found great heterogeneity in the amount of transcriptional changes with age in different tissues. Some tissues displayed large transcriptional differences in old mice, suggesting that these tissues may contribute strongly to organismal decline. Other tissues showed few or no changes in expression with age, indicating strong levels of homeostasis throughout life. Based on the pattern of age-related transcriptional changes, we found that tissues could be classified into one of three aging processes: (1) a pattern common to neural tissues, (2) a pattern for vascular tissues, and (3) a pattern for steroid-responsive tissues. We observed that different tissues age in a coordinated fashion in individual mice, such that certain mice exhibit rapid aging, whereas others exhibit slow aging for multiple tissues. Finally, we compared the transcriptional profiles for aging in mice to those from humans, flies, and worms. We found that genes involved in the electron transport chain show common age regulation in all four species, indicating that these genes may be exceptionally good markers of aging. However, we saw no overall correlation of age regulation between mice and humans, suggesting that aging processes in mice and humans may be fundamentally different. Public Library of Science 2007-11 2007-11-30 /pmc/articles/PMC2098796/ /pubmed/18081424 http://dx.doi.org/10.1371/journal.pgen.0030201 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 Zahn, Jacob M Poosala, Suresh Owen, Art B Ingram, Donald K Lustig, Ana Carter, Arnell Weeraratna, Ashani T Taub, Dennis D Gorospe, Myriam Mazan-Mamczarz, Krystyna Lakatta, Edward G Boheler, Kenneth R Xu, Xiangru Mattson, Mark P Falco, Geppino Ko, Minoru S. H Schlessinger, David Firman, Jeffrey Kummerfeld, Sarah K Wood, William H Zonderman, Alan B Kim, Stuart K Becker, Kevin G AGEMAP: A Gene Expression Database for Aging in Mice |
title | AGEMAP: A Gene Expression Database for Aging in Mice |
title_full | AGEMAP: A Gene Expression Database for Aging in Mice |
title_fullStr | AGEMAP: A Gene Expression Database for Aging in Mice |
title_full_unstemmed | AGEMAP: A Gene Expression Database for Aging in Mice |
title_short | AGEMAP: A Gene Expression Database for Aging in Mice |
title_sort | agemap: a gene expression database for aging in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2098796/ https://www.ncbi.nlm.nih.gov/pubmed/18081424 http://dx.doi.org/10.1371/journal.pgen.0030201 |
work_keys_str_mv | AT zahnjacobm agemapageneexpressiondatabaseforaginginmice AT poosalasuresh agemapageneexpressiondatabaseforaginginmice AT owenartb agemapageneexpressiondatabaseforaginginmice AT ingramdonaldk agemapageneexpressiondatabaseforaginginmice AT lustigana agemapageneexpressiondatabaseforaginginmice AT carterarnell agemapageneexpressiondatabaseforaginginmice AT weeraratnaashanit agemapageneexpressiondatabaseforaginginmice AT taubdennisd agemapageneexpressiondatabaseforaginginmice AT gorospemyriam agemapageneexpressiondatabaseforaginginmice AT mazanmamczarzkrystyna agemapageneexpressiondatabaseforaginginmice AT lakattaedwardg agemapageneexpressiondatabaseforaginginmice AT bohelerkennethr agemapageneexpressiondatabaseforaginginmice AT xuxiangru agemapageneexpressiondatabaseforaginginmice AT mattsonmarkp agemapageneexpressiondatabaseforaginginmice AT falcogeppino agemapageneexpressiondatabaseforaginginmice AT kominorush agemapageneexpressiondatabaseforaginginmice AT schlessingerdavid agemapageneexpressiondatabaseforaginginmice AT firmanjeffrey agemapageneexpressiondatabaseforaginginmice AT kummerfeldsarahk agemapageneexpressiondatabaseforaginginmice AT woodwilliamh agemapageneexpressiondatabaseforaginginmice AT zondermanalanb agemapageneexpressiondatabaseforaginginmice AT kimstuartk agemapageneexpressiondatabaseforaginginmice AT beckerkeving agemapageneexpressiondatabaseforaginginmice |