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pubmed-article:8630255pubmed:abstractTextGene expression regulated by the cAMP response element (CRE) has been implicated in synaptic plasticity and long-term memory. It has been proposed that CRE-mediated gene expression is stimulated by signals that induce long-term potentiation (LTP). To test this hypothesis, we made mice transgenic for a CRE-regulated reporter construct. We focused on long-lasting long-term potentiation (L-LTP), because it depends on cAMP-dependent protein kinase activity (PKA) and de novo gene expression. CRE-mediated gene expression was markedly increased after L-LTP, but not after decremental UP (D-LTP). Furthermore, inhibitors of PKA blocked L-LTP and associated increases in CRE-mediated gene expression. These data demonstrate that the signaling required for the generation of L-LTP but not D-LTP is sufficient to stimulate CRE-mediated transcription in the hippocampus.lld:pubmed
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pubmed-article:8630255pubmed:articleTitleInduction of CRE-mediated gene expression by stimuli that generate long-lasting LTP in area CA1 of the hippocampus.lld:pubmed
pubmed-article:8630255pubmed:affiliationDepartment of Pharmacology, School of Medicine, University of Washington, Seattle, 98195, USA.lld:pubmed
pubmed-article:8630255pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:8630255pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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