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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1995-2-21
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pubmed:abstractText |
Insulin-like growth factor I (IGF-I) is a widely expressed abundant autocrine and paracrine factor that regulates the proliferation and differentiation of a variety of cell types. Prostaglandin E2 (PGE2) is a potent stimulator of IGF-I synthesis in bone. We examined the regulation of IGF-I synthesis by PGE2 in osteoblast-enriched (Ob) cells from fetal rat calvaria. PGE2 treatment of Ob cells at 1 microM for 2 h resulted in a 5-fold increase in heterogeneous nuclear RNA levels, as measured by a reverse transcriptase-polymerase chain reaction assay, suggesting an increase in IGF-I gene transcription. RNase protection analysis was used to map the transcriptional start sites in the IGF-I gene that are used in Ob cells. Consistent with other extrahepatic tissues, initiation of transcription occurs primarily at three sites within the 5'-regions of exon 1 of the IGF-I gene. PGE2 treatment did not alter start site usage. The regions upstream of these transcriptional start sites were analyzed by transiently transfecting Ob cells with putative rat IGF-I promoter sequences ligated to a luciferase reporter gene. Constructs containing 1.4 kilobases of the 5'-regions regions of exons 1 and 2 had significant promoter activity. PGE2 treatment of transfected Ob cells increased luciferase activity 5-fold when a 1.4-kilobase exon 1 promoter fragment was tested. This increase in luciferase activity was time and dose dependent. Smaller regions of the exon 1 promoter sequence gave higher basal activity and were less responsive to PGE2. We conclude that regions involved in IGF-I regulation by PGE2 are contained within the IGF-I promoter.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/Dinoprostone,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor I,
http://linkedlifedata.com/resource/pubmed/chemical/Luciferases,
http://linkedlifedata.com/resource/pubmed/chemical/Oligonucleotide Probes,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0013-7227
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
136
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
33-8
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:7828549-Animals,
pubmed-meshheading:7828549-Base Sequence,
pubmed-meshheading:7828549-DNA,
pubmed-meshheading:7828549-Dinoprostone,
pubmed-meshheading:7828549-Embryo, Mammalian,
pubmed-meshheading:7828549-Exons,
pubmed-meshheading:7828549-Insulin-Like Growth Factor I,
pubmed-meshheading:7828549-Luciferases,
pubmed-meshheading:7828549-Molecular Sequence Data,
pubmed-meshheading:7828549-Oligonucleotide Probes,
pubmed-meshheading:7828549-Osteoblasts,
pubmed-meshheading:7828549-Polymerase Chain Reaction,
pubmed-meshheading:7828549-Promoter Regions, Genetic,
pubmed-meshheading:7828549-RNA, Messenger,
pubmed-meshheading:7828549-Rats,
pubmed-meshheading:7828549-Skull,
pubmed-meshheading:7828549-Transcription, Genetic
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pubmed:year |
1995
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pubmed:articleTitle |
Regulation of insulin-like growth factor I transcription by prostaglandin E2 in osteoblast cells.
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pubmed:affiliation |
Department of Research, Saint Francis Hospital and Medical Center, Hartford, Connecticut 06105.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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