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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1994-11-4
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pubmed:abstractText |
We have investigated the retinoic acid-mediated activation of the transcriptional regulator HNF-3 beta during differentiation of mouse F9 embryonal carcinoma cells. Using gel shifts, HNF-3 beta DNA binding activity was clearly detected in differentiated cells, while F9 stem cells were devoid of this activity. We also demonstrated that HNF-3 beta mRNA is specific for differentiated cells. Addition of retinoic acid to F9 stem cells results in delayed activation of HNF-3 beta mRNA which can be detected 1-2 days after the initiation of differentiation. HNF-3 beta mRNA concentrations are maximal at approximately 4 days postdifferentiation and stay at elevated levels for at least 4 additional days. Nuclear run-on experiments clearly show that HNF-3 beta is activated at the level of transcriptional initiation, suggesting that the increases of beta-specific DNA binding activity and mRNA concentration are merely a reflection of this activation mechanism. F9 cells can give rise to three distinct differentiated cell types, visceral endoderm, parietal endoderm, and primitive endoderm, and we have observed HNF-3 beta stimulation during the formation of all three tissues. HNF-3 beta stimulation upon visceral endoderm differentiation is accompanied by the activation of HNF-3 target genes such as transthyretin, suggesting that HNF-3 beta is involved in the developmental activation of this gene. In contrast, HNF-3 beta target genes in parietal and primitive endoderm have yet to be identified. However, the stimulation of HNF-3 beta during primitive endoderm formation, which is an extremely early event during murine embryogenesis, points toward a role for the factor in crucial determination processes that occur early during development.
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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/Foxa2 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Hepatocyte Nuclear Factor 3-beta,
http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/Tretinoin
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0014-4827
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
214
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
634-41
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7925656-Animals,
pubmed-meshheading:7925656-Base Sequence,
pubmed-meshheading:7925656-Cell Differentiation,
pubmed-meshheading:7925656-DNA-Binding Proteins,
pubmed-meshheading:7925656-Endoderm,
pubmed-meshheading:7925656-Gene Expression Regulation,
pubmed-meshheading:7925656-Hepatocyte Nuclear Factor 3-beta,
pubmed-meshheading:7925656-Mice,
pubmed-meshheading:7925656-Molecular Sequence Data,
pubmed-meshheading:7925656-Nuclear Proteins,
pubmed-meshheading:7925656-RNA, Messenger,
pubmed-meshheading:7925656-Teratocarcinoma,
pubmed-meshheading:7925656-Time Factors,
pubmed-meshheading:7925656-Transcription, Genetic,
pubmed-meshheading:7925656-Transcription Factors,
pubmed-meshheading:7925656-Tretinoin,
pubmed-meshheading:7925656-Tumor Cells, Cultured
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pubmed:year |
1994
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pubmed:articleTitle |
Delayed activation of HNF-3 beta upon retinoic acid-induced teratocarcinoma cell differentiation.
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pubmed:affiliation |
Department of Pharmacology and Molecular Biology, Chicago Medical School, Illinois 60064.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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