Impaired extinction of learned contextual fear memory in early growth response 1 knockout mice

Inductive expression of early growth response 1 (Egr-1) in neurons is associated with many forms of neuronal activity. However, only a few Egr-1 target genes are known in the brain. The results of this study demonstrate that Egr-1 knockout (KO) mice display impaired contextual extinction learning an...

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Veröffentlicht in:Molecules and cells 2014, 37(1), , pp.24-30
Hauptverfasser: Han, Seungrie, Hong, Soontaek, Mo, Jiwon, Lee, Dongmin, Choi, Eunju, Choi, June-seek, Sun, Woong, Lee, Hyun Woo, Kim, Hyun
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Sprache:eng
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Zusammenfassung:Inductive expression of early growth response 1 (Egr-1) in neurons is associated with many forms of neuronal activity. However, only a few Egr-1 target genes are known in the brain. The results of this study demonstrate that Egr-1 knockout (KO) mice display impaired contextual extinction learning and normal fear acquisition relative to wild-type (WT) control animals. Genome-wide microarray experiments revealed 368 differentially expressed genes in the hippocampus of Egr-1 WT exposed to different phases of a fear conditioning paradigm compared to gene expression profiles in the hippocampus of KO mice. Some of genes, such as serotonin receptor 2C (Htr2c), neuropeptide B (Npb), neuronal PAS domain protein 4 (Npas4), NPY receptor Y1 (Npy1r), fatty acid binding protein 7 (Fabp7), and neuropeptide Y (Npy) are known to regulate processing of fearful memories, and promoter analyses demonstrated that several of these genes contained Egr-1 binding sites. This study provides a useful list of potential Egr-1 target genes which may be regulated during fear memory processing.
ISSN:1016-8478
0219-1032
DOI:10.14348/molcells.2014.2206