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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
2004-9-28
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pubmed:abstractText |
CREB-binding protein (CBP) is an important transcriptional cofactor for various intracellular signaling pathways, including Ca(2+)- and cAMP-mediated gene activation. The loss of one CBP allele causes the human Rubinstein-Taybi syndrome, which is characterized by mental retardation and other severe developmental defects. Deletion of both CBP alleles in the mouse leads to early embryonic lethality. To address the function of CBP in late embryogenesis and in adult physiology, a floxed CBP allele (CBP(fl)) was generated. Using the Cre/loxP recombination system, CBP function was disrupted in principal forebrain neurons by breeding with a transgenic CaMKIIalpha-Cre mouse line to obtain CBP(fl/fl;CaMKIIalphaCre) mice. These mice contain CBP(stop523) alleles specifically in principal forebrain neurons, presumably resulting in the production of a truncated CBP protein unable to interact with a number of transcription factors, including phosphorylated CREB.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1526-954X
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pubmed:author |
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pubmed:copyrightInfo |
Copyright 2004 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:volume |
40
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
82-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15452871-Alleles,
pubmed-meshheading:15452871-Animals,
pubmed-meshheading:15452871-CREB-Binding Protein,
pubmed-meshheading:15452871-Chromosome Mapping,
pubmed-meshheading:15452871-Electroporation,
pubmed-meshheading:15452871-Embryonic Development,
pubmed-meshheading:15452871-Exons,
pubmed-meshheading:15452871-Gene Deletion,
pubmed-meshheading:15452871-Gene Targeting,
pubmed-meshheading:15452871-Heterozygote,
pubmed-meshheading:15452871-Hippocampus,
pubmed-meshheading:15452871-Homozygote,
pubmed-meshheading:15452871-In Situ Hybridization,
pubmed-meshheading:15452871-Integrases,
pubmed-meshheading:15452871-Mice,
pubmed-meshheading:15452871-Mice, Mutant Strains,
pubmed-meshheading:15452871-Mice, Transgenic,
pubmed-meshheading:15452871-Neurons,
pubmed-meshheading:15452871-Nuclear Proteins,
pubmed-meshheading:15452871-Polymerase Chain Reaction,
pubmed-meshheading:15452871-Prosencephalon,
pubmed-meshheading:15452871-Recombination, Genetic,
pubmed-meshheading:15452871-Stem Cells,
pubmed-meshheading:15452871-Trans-Activators,
pubmed-meshheading:15452871-Viral Proteins
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pubmed:year |
2004
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pubmed:articleTitle |
Generation of a conditional allele of the CBP gene in mouse.
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pubmed:affiliation |
Molecular Genetics of Behavior, Max Planck Institute of Psychiatry, Kraepelinstrasse 2-10, 80804 Munich, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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