rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
1999-5-19
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pubmed:abstractText |
Recruitment of the coactivator CBP by signal-regulated transcription factors and stimulation of CBP activity are key regulatory events in the induction of gene transcription following Ca2+ flux through ligand- and/or voltage-gated ion channels in hippocampal neurons. The mode of Ca2+ entry (L-type Ca2+ channels versus NMDA receptors) differentially controls the CBP recruitment step to CREB, providing a molecular basis for the observed Ca2+ channel type-dependent differences in gene expression. In contrast, activation of CBP is triggered irrespective of the route of Ca2+ entry, as is activation of c-Jun, that recruits CBP independently of phosphorylation at major regulatory c-Jun phosphorylation sites, serines 63 and 73. This control of CBP recruitment and activation is likely relevant to other CBP-interacting transcription factors and represents a general mechanism through which Ca2+ signals associated with electrical activity may regulate the expression of many genes.
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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 |
http://linkedlifedata.com/resource/pubmed/chemical/CREB-Binding Protein,
http://linkedlifedata.com/resource/pubmed/chemical/CREBBP protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-fos,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, N-Methyl-D-Aspartate,
http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0896-6273
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
789-98
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:10230798-CREB-Binding Protein,
pubmed-meshheading:10230798-Calcium,
pubmed-meshheading:10230798-Calcium Channels,
pubmed-meshheading:10230798-Cells, Cultured,
pubmed-meshheading:10230798-Gene Expression Regulation,
pubmed-meshheading:10230798-Hippocampus,
pubmed-meshheading:10230798-Humans,
pubmed-meshheading:10230798-Membrane Potentials,
pubmed-meshheading:10230798-Nerve Tissue Proteins,
pubmed-meshheading:10230798-Neurons,
pubmed-meshheading:10230798-Nuclear Proteins,
pubmed-meshheading:10230798-Phosphorylation,
pubmed-meshheading:10230798-Proto-Oncogene Proteins c-fos,
pubmed-meshheading:10230798-Receptors, N-Methyl-D-Aspartate,
pubmed-meshheading:10230798-Recruitment, Neurophysiological,
pubmed-meshheading:10230798-Trans-Activators,
pubmed-meshheading:10230798-Transcriptional Activation
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pubmed:year |
1999
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pubmed:articleTitle |
Control of recruitment and transcription-activating function of CBP determines gene regulation by NMDA receptors and L-type calcium channels.
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pubmed:affiliation |
Medical Research Council, Laboratory of Molecular Biology, Cambridge, United Kingdom.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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