Source:http://linkedlifedata.com/resource/pubmed/id/15532030
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2004-11-30
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pubmed:abstractText |
The Brn-3a transcription factor is critical for survival and differentiation of sensory neurons derived from neural crest cells (NCC). Interaction of Brn-3a with p53 results in differential effects on target gene expression, which profoundly affects fate of neuronal cells. Here we demonstrate colocalization of p53 in a subset of Brn-3a-positive NCC-derived cells fated for the sensory neuronal lineage. The distinct morphology of Brn-3a/p53-coexpressing cells suggested a differentiated neuronal cell type, and this was confirmed by colocalization of p53 with differentiation marker NF-160. Functional effects of Brn-3a/p53 coexpression were analyzed in NCC cultured from Brn-3a -/- embryos, which showed significantly increased apoptosis upon induction of p53 compared with wild-type NCC, suggesting that Brn-3a modulates the p53-mediated fate of NCC that coexpress both factors. Thus, p53 is expressed in neuronal cells undergoing differentiation as well as apoptosis. Interaction with Brn-3a in sensory neurons may be critical for modulating p53-mediated gene expression and hence cell fate.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Pou4f1 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factor Brn-3,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factor Brn-3A,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Protein p53
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0360-4012
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pubmed:author | |
pubmed:copyrightInfo |
(c) 2004 Wiley-Liss, Inc.
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
78
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
803-14
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:15532030-Animals,
pubmed-meshheading:15532030-Apoptosis,
pubmed-meshheading:15532030-Cell Differentiation,
pubmed-meshheading:15532030-Cells, Cultured,
pubmed-meshheading:15532030-DNA-Binding Proteins,
pubmed-meshheading:15532030-Embryo, Mammalian,
pubmed-meshheading:15532030-Gene Expression Regulation, Developmental,
pubmed-meshheading:15532030-Mice,
pubmed-meshheading:15532030-Mice, Knockout,
pubmed-meshheading:15532030-Nervous System,
pubmed-meshheading:15532030-Neurons,
pubmed-meshheading:15532030-Stem Cells,
pubmed-meshheading:15532030-Transcription Factor Brn-3,
pubmed-meshheading:15532030-Transcription Factor Brn-3A,
pubmed-meshheading:15532030-Transcription Factors,
pubmed-meshheading:15532030-Tumor Suppressor Protein p53
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pubmed:year |
2004
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pubmed:articleTitle |
Coexpression of Brn-3a POU protein with p53 in a population of neuronal progenitor cells is associated with differentiation and protection against apoptosis.
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pubmed:affiliation |
Medical Molecular Biology Unit, Institute of Child Health, London, United Kingdom.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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