Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
49
pubmed:dateCreated
2000-2-3
pubmed:abstractText
We previously identified various upstream and downstream regulatory elements and factors important for hepatic expression of the human angiotensinogen (ANG) gene, the precursor of vasoactive octapeptide angiotensin II. In the present study, to further investigate the molecular mechanism of human ANG transcriptional regulation, we generated transgenic mice carrying the fusion gene composed of the 1. 3-kilobase promoter of the human ANG gene, its downstream enhancer, and the chloramphenicol acetyltransferase reporter gene. Because expression of the chloramphenicol acetyltransferase gene was observed strongly in the liver and weakly in the kidney, we suspected that hepatocyte nuclear factor (HNF) 4 with a tissue expression pattern similar to that of the reporter gene would regulate ANG transcription. In vitro assays indicated that HNF4 bound to the promoter elements and strongly activated the ANG transcription, but that chicken ovalbumin upstream promoter transcription factor (COUP-TF), a transcriptional repressor, dramatically repressed human ANG transcription through the promoter elements and the downstream enhancer core elements. Furthermore, COUP-TF dramatically decreased the human ANG transcription in the mouse liver by the Helios Gene Gun system in vivo. These results suggest that an interplay between HNF4 and COUP-TF could be important in hepatic human ANG transcription.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Angiotensins, http://linkedlifedata.com/resource/pubmed/chemical/Basic Helix-Loop-Helix Leucine..., http://linkedlifedata.com/resource/pubmed/chemical/COUP Transcription Factor I, http://linkedlifedata.com/resource/pubmed/chemical/Chloramphenicol O-Acetyltransferase, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Hepatocyte Nuclear Factor 4, http://linkedlifedata.com/resource/pubmed/chemical/MLX protein, human, http://linkedlifedata.com/resource/pubmed/chemical/NR2F1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Nr2f1 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Phosphoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Tcfl4 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
3
pubmed:volume
274
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
34605-12
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:10574924-Angiotensins, pubmed-meshheading:10574924-Animals, pubmed-meshheading:10574924-Base Sequence, pubmed-meshheading:10574924-Basic Helix-Loop-Helix Leucine Zipper Transcription Factors, pubmed-meshheading:10574924-Binding Sites, pubmed-meshheading:10574924-COUP Transcription Factor I, pubmed-meshheading:10574924-Cell Nucleus, pubmed-meshheading:10574924-Chloramphenicol O-Acetyltransferase, pubmed-meshheading:10574924-DNA-Binding Proteins, pubmed-meshheading:10574924-Dose-Response Relationship, Drug, pubmed-meshheading:10574924-Gene Deletion, pubmed-meshheading:10574924-Gene Expression Regulation, pubmed-meshheading:10574924-Hepatocyte Nuclear Factor 4, pubmed-meshheading:10574924-Humans, pubmed-meshheading:10574924-Liver, pubmed-meshheading:10574924-Mice, pubmed-meshheading:10574924-Mice, Inbred C57BL, pubmed-meshheading:10574924-Mice, Inbred ICR, pubmed-meshheading:10574924-Mice, Transgenic, pubmed-meshheading:10574924-Molecular Sequence Data, pubmed-meshheading:10574924-Phosphoproteins, pubmed-meshheading:10574924-Protein Binding, pubmed-meshheading:10574924-Response Elements, pubmed-meshheading:10574924-Transcription, Genetic, pubmed-meshheading:10574924-Transcription Factors, pubmed-meshheading:10574924-Tumor Cells, Cultured
pubmed:year
1999
pubmed:articleTitle
Regulated expression of human angiotensinogen gene by hepatocyte nuclear factor 4 and chicken ovalbumin upstream promoter-transcription factor.
pubmed:affiliation
Center for Tsukuba Advanced Research Alliance, University of Tsukuba, Ibaraki 305-8577, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't