Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
34
pubmed:dateCreated
2008-8-21
pubmed:abstractText
Cytoplasmic polyadenylation element binding protein 1 (CPEB-1) resides at postsynaptic sites in hippocampal neurons in which it controls polyadenylation-induced translation. CPEB-1 knock-out (KO) mice display defects in some forms of synaptic plasticity and hippocampal-dependent memories. To identify CPEB-1-regulated mRNAs, we used proteomics to compare polypeptides in wild-type (WT) and CPEB-1 KO hippocampus. Growth hormone (GH) was reduced in the KO hippocampus, as were the GH signaling molecules phospho-JAK2 and phospho-STAT3. GH mRNA and pre-mRNA were reduced in the KO hippocampus, suggesting that CPEB-1 controls GH transcription. The transcription factor c-Jun, which binds the GH promoter, was also reduced in the KO hippocampus, as was its ability to coimmunoprecipitate chromatin containing the GH promoter. CPEB-1 binds c-Jun 3' untranslated region CPEs in vitro and coimmunoprecipitates c-Jun RNA in vivo. GH induces long-term potentiation (LTP) when applied to hippocampal slices from WT and CPEB-1 KO mice, but the magnitude of LTP induced by GH in KO mice is reduced. Pretreatment with GH did not reverse the LTP deficit observed in KO mice after theta-burst stimulation (TBS). Cordycepin, an inhibitor of polyadenylation, disrupted LTP induced by either GH application or TBS. Finally, GH application to hippocampal slices induced JAK2 phosphorylation in WT but not KO animals. These results indicate that CPEB-1 control of c-Jun mRNA translation regulates GH gene expression and resulting downstream signaling events (e.g., synaptic plasticity) in the mouse hippocampus.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1529-2401
pubmed:author
pubmed:issnType
Electronic
pubmed:day
20
pubmed:volume
28
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
8502-9
pubmed:meshHeading
pubmed-meshheading:18716208-Animals, pubmed-meshheading:18716208-Down-Regulation, pubmed-meshheading:18716208-Electric Stimulation, pubmed-meshheading:18716208-Electrophysiology, pubmed-meshheading:18716208-Growth Hormone, pubmed-meshheading:18716208-Hippocampus, pubmed-meshheading:18716208-Humans, pubmed-meshheading:18716208-Long-Term Potentiation, pubmed-meshheading:18716208-Male, pubmed-meshheading:18716208-Mice, pubmed-meshheading:18716208-Mice, Inbred C57BL, pubmed-meshheading:18716208-Mice, Knockout, pubmed-meshheading:18716208-Neuronal Plasticity, pubmed-meshheading:18716208-Protein Biosynthesis, pubmed-meshheading:18716208-Proteomics, pubmed-meshheading:18716208-Proto-Oncogene Proteins c-jun, pubmed-meshheading:18716208-RNA, Messenger, pubmed-meshheading:18716208-RNA Precursors, pubmed-meshheading:18716208-Recombinant Proteins, pubmed-meshheading:18716208-Synapses, pubmed-meshheading:18716208-Transcription, Genetic, pubmed-meshheading:18716208-Transcription Factors, pubmed-meshheading:18716208-mRNA Cleavage and Polyadenylation Factors
pubmed:year
2008
pubmed:articleTitle
A molecular circuit composed of CPEB-1 and c-Jun controls growth hormone-mediated synaptic plasticity in the mouse hippocampus.
pubmed:affiliation
Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts 01605, USA.
pubmed:publicationType
Journal Article, In Vitro, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural