rdf:type |
|
lifeskim:mentions |
umls-concept:C0003577,
umls-concept:C0017262,
umls-concept:C0027882,
umls-concept:C0028608,
umls-concept:C0185117,
umls-concept:C0205263,
umls-concept:C0234112,
umls-concept:C0443252,
umls-concept:C1414236,
umls-concept:C1415090,
umls-concept:C1514873,
umls-concept:C1546857,
umls-concept:C1556066,
umls-concept:C1619636,
umls-concept:C1837550,
umls-concept:C2911684
|
pubmed:issue |
5
|
pubmed:dateCreated |
2006-2-28
|
pubmed:abstractText |
In Aplysia, long-term synaptic plasticity is induced by serotonin (5-HT) or neural activity and requires gene expression. Here, we demonstrate that ApLLP, a novel nucleolus protein, is critically involved in both long-term facilitation (LTF) and behavioral sensitization. Membrane depolarization induced ApLLP expression, which activated ApC/EBP expression through a direct binding to CRE. LTF was produced by a single pulse of 5-HT 30 min after the membrane depolarization. This LTF was blocked when either ApLLP or ApC/EBP were blocked by specific antibodies. In contrast, ApLLP overexpression induced LTF in response to a single 5-HT treatment. Simultaneously, a siphon noxious stimulus (SNS) to intact Aplysia induced ApLLP and ApC/EBP expression, and single tail shock 30 min after SNS transformed short-term sensitization to long-term sensitization of siphon withdrawal reflex. These results suggest that ApLLP is an activity-dependent transcriptional activator that switches short-term facilitation to long-term facilitation.
|
pubmed:commentsCorrections |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0896-6273
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
2
|
pubmed:volume |
49
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
707-18
|
pubmed:dateRevised |
2008-11-21
|
pubmed:meshHeading |
pubmed-meshheading:16504946-Analysis of Variance,
pubmed-meshheading:16504946-Animals,
pubmed-meshheading:16504946-Aplysia,
pubmed-meshheading:16504946-Avoidance Learning,
pubmed-meshheading:16504946-Behavior, Animal,
pubmed-meshheading:16504946-Blotting, Western,
pubmed-meshheading:16504946-CCAAT-Enhancer-Binding Proteins,
pubmed-meshheading:16504946-Cells, Cultured,
pubmed-meshheading:16504946-Dose-Response Relationship, Drug,
pubmed-meshheading:16504946-Electric Stimulation,
pubmed-meshheading:16504946-Electrophoretic Mobility Shift Assay,
pubmed-meshheading:16504946-Gene Expression,
pubmed-meshheading:16504946-Gene Expression Regulation,
pubmed-meshheading:16504946-Green Fluorescent Proteins,
pubmed-meshheading:16504946-Immunohistochemistry,
pubmed-meshheading:16504946-In Situ Hybridization,
pubmed-meshheading:16504946-Long-Term Potentiation,
pubmed-meshheading:16504946-Microinjections,
pubmed-meshheading:16504946-Models, Biological,
pubmed-meshheading:16504946-Neurons,
pubmed-meshheading:16504946-Potassium,
pubmed-meshheading:16504946-Promoter Regions, Genetic,
pubmed-meshheading:16504946-RNA, Messenger,
pubmed-meshheading:16504946-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:16504946-Serotonin,
pubmed-meshheading:16504946-Time Factors,
pubmed-meshheading:16504946-Transcription Factors,
pubmed-meshheading:16504946-Transcriptional Activation
|
pubmed:year |
2006
|
pubmed:articleTitle |
A nucleolar protein ApLLP induces ApC/EBP expression required for long-term synaptic facilitation in aplysia neurons.
|
pubmed:affiliation |
National Research Laboratory, Institute of Molecular Biology and Genetics, School of Biological Sciences, College of Natural Sciences, Seoul National University, San 56-1 Silim-dong Kwanak-gu, Seoul 151-742, Korea.
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|