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  AGEMAP: a gene expression database for aging in mice

Zahn, J. M., Poosala, S., Owen, A. B., Ingram, D. K., Lustig, A., Carter, A., et al. (2007). AGEMAP: a gene expression database for aging in mice. PLoS Genet, 3(11), e201. doi:10.1371/journal.pgen.0030201.

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Genre: Zeitschriftenartikel

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externe Referenz:
https://www.ncbi.nlm.nih.gov/pubmed/18081424 (beliebiger Volltext)
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Keine Angabe

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Zahn, J. M., Autor
Poosala, S., Autor
Owen, A. B., Autor
Ingram, D. K., Autor
Lustig, A., Autor
Carter, A., Autor
Weeraratna, A. T., Autor
Taub, D. D., Autor
Gorospe, M., Autor
Mazan-Mamczarz, K., Autor
Lakatta, E. G., Autor
Boheler, K. R., Autor
Xu, X.1, Autor           
Mattson, M. P., Autor
Falco, G., Autor
Ko, M. S., Autor
Schlessinger, D., Autor
Firman, J., Autor
Kummerfeld, S. K., Autor
Wood, W. H., 3rd, Autor
Zonderman, A. B., AutorKim, S. K., AutorBecker, K. G., Autor mehr..
Affiliations:
1Xu – Epigenetic Regulation of Mammalian Ageing, Research Groups, Max Planck Institute for Biology of Ageing, Max Planck Society, ou_3394009              

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Schlagwörter: Aging/*genetics Animals *Databases, Genetic Diptera/genetics Gene Expression Profiling *Gene Expression Regulation Helminths/genetics Humans Mice Organ Specificity Species Specificity
 Zusammenfassung: 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.

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 Datum: 2007-112007
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: Anderer: 18081424
DOI: 10.1371/journal.pgen.0030201
ISSN: 1553-7404 (Electronic)1553-7390 (Linking)
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Quelle 1

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Titel: PLoS Genet
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 3 (11) Artikelnummer: - Start- / Endseite: e201 Identifikator: -