GeneSet Information

Tier III GS137849 • Aging and learning-related genes in the hippocampus dentate gyrus of aged-superior learners (SL) vs. age learning-impaired (AI) vs. young rats

DESCRIPTION:

Two rounds of RNA amplification were performed on RNA from the hippocampal dentate gyri of 3-month-old young and 24-month-old aged-superior learners (SL) and age learning-impaired (AI) Fischer 344 male rats. P-values were uploaded.

LABEL:

Rat Diff Age and Abilities

SCORE TYPE:

P-Value

DATE ADDED:

None

DATE UPDATED:

2024-04-25

SPECIES:

AUTHORS:

Burger C, Lopez MC, Baker HV, Mandel RJ, Muzyczka N

TITLE:

Genome-wide analysis of aging and learning-related genes in the hippocampal dentate gyrus.

JOURNAL:

Neurobiology of learning and memory May 2008, Vol 89, pp. 379-96

ABSTRACT:

We have previously described the transcriptional changes that occur in the hippocampal CA1 field of aged rats following a Morris Water Maze (MWM) training paradigm. In this report we proceed with the analysis of the dentate region from the same animals. Animals were first identified as age learning-impaired or age-superior learners when compared to young rats based on their performance in the MWM. Messenger RNA was isolated from the dentate gyrus of each animal to interrogate Affymetrix RAE 230A rat genome microarrays. Microarray profiling identified 1129 genes that were differentially expressed between aged and young rats as a result of aging, and independent of their behavioral training (p<0.005). We applied Ingenuity Pathway Analysis (IPA) algorithms to identify the significant biological processes underlying age-related changes in the dentate gyrus. The most significant functions, as calculated by IPA, included cell movement, cell growth and proliferation, nervous system development and function, cellular assembly and organization, cell morphology and cell death. These significant processes are consistent with age-related changes in neurogenesis, and the neurogenic markers were generally found to be downregulated in senescent animals. In addition, statistical analysis of the different experimental groups of aged animals recognized 85 genes (p<0.005) that were different in the dentate gyrus of aged rats that had learned the MWM when compared to learning impaired and a number of controls for stress, exercise and non-spatial learning. The list of learning-related genes expressed in the dentate adds to the set of genes we previously described in the CA1 region. This long list of genes constitutes a starting tool to elucidating the molecular pathways involved in learning and memory formation. PUBMED: 18234529
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Annotation Information

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Cell Movement (D002465)
Animals (D000818)
Exercise (D015444)
Research Report (D058028)
Biological Processes (D055694)
Movement (D009068)
Dentate Gyrus (D018891)
RNA, Messenger (D012333)
Neurogenesis (D055495)
Nervous System (D009420)
Cell Death (D016923)
Learning (D007858)
Organizations (D009938)
Algorithms (D000465)
Independent Practice Associations (D007193)
Set (Psychology) (D012718)
nervous system (MA:0000016)
dentate gyrus (MA:0000190)
cell death (GO:0008219)
nervous system development (GO:0007399)
neurogenesis (GO:0022008)
biosynthetic process (GO:0009058)
system development (GO:0048731)
cell growth (GO:0016049)

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