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dc.contributor.authorWu, Lin
dc.contributor.authorWells, David G.
dc.contributor.authorTay, Joyce
dc.contributor.authorMendis, Duane
dc.contributor.authorAbbott, Mary-Alice
dc.contributor.authorBarnitt, Allan
dc.contributor.authorQuinlan, Elizabeth
dc.contributor.authorHeynen, Arnold
dc.contributor.authorFallon, Justin R.
dc.contributor.authorRichter, Joel D.
dc.date2022-08-11T08:09:02.000
dc.date.accessioned2022-08-23T16:16:17Z
dc.date.available2022-08-23T16:16:17Z
dc.date.issued1998-12-18
dc.date.submitted2008-11-25
dc.identifier.citation<p>Neuron. 1998 Nov;21(5):1129-39.</p>
dc.identifier.issn0896-6273 (Print)
dc.identifier.doihttps://escholarship.umassmed.edu/gsbs_sp/949
dc.identifier.pmid9856468
dc.identifier.urihttp://hdl.handle.net/20.500.14038/34297
dc.description.abstractLong-term changes in synaptic efficacy may require the regulated translation of dendritic mRNAs. While the basis of such regulation is unknown, it seemed possible that some features of translational control in development could be recapitulated in neurons. Polyadenylation-induced translation of oocyte mRNAs requires the cis-acting CPE sequence and the CPE-binding protein CPEB. CPEB is also present in the dendritic layers of the hippocampus, at synapses in cultured neurons, and in postsynaptic densities of adult brain. alpha-CaMKII mRNA, which is localized in dendrites and is necessary for synaptic plasticity and LTP, contains two CPEs. These CPEs are bound by CPEB and mediate polyadenylation-induced translation in injected Xenopus oocytes. In the intact brain, visual experience induces alpha-CaMKII mRNA polyadenylation and translation, suggesting that this process likely occurs at synapses.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=9856468&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1016/S0896-6273(00)80630-3
dc.subjectAnimals; Brain; Calcium-Calmodulin-Dependent Protein Kinase Type 2; Calcium-Calmodulin-Dependent Protein Kinases; Cells, Cultured; Cytoplasm; Hippocampus; Mice; Neurons; Oocytes; Organ Specificity; RNA, Messenger; RNA-Binding Proteins; Rats; Rats, Long-Evans; Rats, Wistar; Synapses; Transcription Factors; Xenopus; *Xenopus Proteins; *mRNA Cleavage and Polyadenylation Factors
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleCPEB-mediated cytoplasmic polyadenylation and the regulation of experience-dependent translation of alpha-CaMKII mRNA at synapses
dc.typeJournal Article
dc.source.journaltitleNeuron
dc.source.volume21
dc.source.issue5
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/949
dc.identifier.contextkey672222
html.description.abstract<p>Long-term changes in synaptic efficacy may require the regulated translation of dendritic mRNAs. While the basis of such regulation is unknown, it seemed possible that some features of translational control in development could be recapitulated in neurons. Polyadenylation-induced translation of oocyte mRNAs requires the cis-acting CPE sequence and the CPE-binding protein CPEB. CPEB is also present in the dendritic layers of the hippocampus, at synapses in cultured neurons, and in postsynaptic densities of adult brain. alpha-CaMKII mRNA, which is localized in dendrites and is necessary for synaptic plasticity and LTP, contains two CPEs. These CPEs are bound by CPEB and mediate polyadenylation-induced translation in injected Xenopus oocytes. In the intact brain, visual experience induces alpha-CaMKII mRNA polyadenylation and translation, suggesting that this process likely occurs at synapses.</p>
dc.identifier.submissionpathgsbs_sp/949
dc.contributor.departmentProgram in Molecular Medicine
dc.contributor.departmentDepartment of Molecular Genetics and Microbiology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages1129-39


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