AGEMAP: A gene expression database for aging in mice

被引:289
作者
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.
Ill, William H. Wood
Zonderman, Alan B.
Kim, Stuart K. [1 ]
Becker, Kevin G.
机构
[1] Stanford Univ, Dept Dev Biol, Med Ctr, Stanford, CA 94305 USA
[2] NIA, NIH, Baltimore, MD 21224 USA
[3] Stanford Univ, Dept Stat, Stanford, CA 94305 USA
[4] Stanford Univ, Med Ctr, Dept Genet, Stanford, CA 94305 USA
来源
PLOS GENETICS | 2007年 / 3卷 / 11期
关键词
D O I
10.1371/journal.pgen.0030201
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:2326 / 2337
页数:12
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