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- Publisher Website: 10.1371/journal.pgen.0030201
- Scopus: eid_2-s2.0-37249049422
- PMID: 18081424
- WOS: WOS:000251310200024
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Article: AGEMAP: A gene expression database for aging in mice
Title | AGEMAP: A gene expression database for aging in mice |
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Authors | |
Issue Date | 2007 |
Citation | PLoS Genetics, 2007, v. 3 n. 11, p. 2326-2337 How to Cite? |
Abstract | 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 agerelated 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. |
Persistent Identifier | http://hdl.handle.net/10722/195188 |
ISSN | 2014 Impact Factor: 7.528 2023 SCImago Journal Rankings: 2.219 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Zahn, JM | - |
dc.contributor.author | Poosala, S | - |
dc.contributor.author | Owen, AB | - |
dc.contributor.author | Ingram, DK | - |
dc.contributor.author | Lustig, A | - |
dc.contributor.author | Carter, A | - |
dc.contributor.author | Weeraratna, AT | - |
dc.contributor.author | Taub, DD | - |
dc.contributor.author | Gorospe, M | - |
dc.contributor.author | Mazan-Mamczarz, K | - |
dc.contributor.author | Lakatta, EG | - |
dc.contributor.author | Boheler, KR | - |
dc.contributor.author | Xu, X | - |
dc.contributor.author | Mattson, MP | - |
dc.contributor.author | Falco, G | - |
dc.contributor.author | Ko, MSH | - |
dc.contributor.author | Schlessinger, D | - |
dc.contributor.author | Firman, J | - |
dc.contributor.author | Kummerfeld, SK | - |
dc.contributor.author | Wood III, WH | - |
dc.contributor.author | Zonderman, AB | - |
dc.contributor.author | Kim, SK | - |
dc.contributor.author | Becker, KG | - |
dc.date.accessioned | 2014-02-25T01:40:17Z | - |
dc.date.available | 2014-02-25T01:40:17Z | - |
dc.date.issued | 2007 | - |
dc.identifier.citation | PLoS Genetics, 2007, v. 3 n. 11, p. 2326-2337 | - |
dc.identifier.issn | 1553-7390 | - |
dc.identifier.uri | http://hdl.handle.net/10722/195188 | - |
dc.description.abstract | 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 agerelated 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. | - |
dc.language | eng | - |
dc.relation.ispartof | PLoS Genetics | - |
dc.title | AGEMAP: A gene expression database for aging in mice | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1371/journal.pgen.0030201 | - |
dc.identifier.pmid | 18081424 | - |
dc.identifier.scopus | eid_2-s2.0-37249049422 | - |
dc.identifier.volume | 3 | - |
dc.identifier.issue | 11 | - |
dc.identifier.spage | 2326 | - |
dc.identifier.epage | 2337 | - |
dc.identifier.isi | WOS:000251310200024 | - |
dc.identifier.issnl | 1553-7390 | - |