Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2002-1-11
pubmed:abstractText
We previously generated a transgenic mouse line (T-77) in which increased hepatic expression of the hepatocyte nuclear factor-3beta (HNF-3beta) protein was used to assess its role in hepatocyte-specific gene transcription. The T-77 transgenic mice displayed elevated serum bile acid and bilirubin levels and a complete absence of hepatic glycogen storage. These postnatal liver defects were associated with diminished expression of hepatocyte genes involved in gluconeogenesis and bile acid transport as well as reduced levels of hepatocyte transcription factors. In this study, we show that mouse tail vein injections of adenovirus expressing the rat HNF-3beta (AdHNF3beta) cDNA efficiently increased its levels throughout the liver lobule and recapitulated the T-77 transgenic liver phenotype within several days postinfection. Likewise, the AdHNF3beta-infected liver phenotype was associated with reduced hepatic expression of genes involved in glucose homeostasis, bile acid transport, and bilirubin conjugation, which were not found with control adenovirus infections. These studies show that adenovirus-mediated gene transfer is an effective method for rapid hepatic increases in transcription factor levels to determine in vivo target genes. In contrast, AdHNF3alpha-infected liver displayed only a transient reduction in hepatic glycogen levels and was associated with less severe decreases in hepatic expression of gluconeogenic and bilirubin metabolism genes. Consistent with these findings, only T-77 transgenic and AdHNF3beta-infected liver exhibited diminished hepatic expression of the HNF-6 transcription factor, suggesting that reduced HNF-6 levels contribute to diminished HNF-3beta-specific transcriptional activity.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/AKR1C2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Foxa1 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Foxa2 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Glucose, http://linkedlifedata.com/resource/pubmed/chemical/Glucose-6-Phosphatase, http://linkedlifedata.com/resource/pubmed/chemical/Glucuronosyltransferase, http://linkedlifedata.com/resource/pubmed/chemical/Glycogen, http://linkedlifedata.com/resource/pubmed/chemical/Hepatocyte Nuclear Factor 3-alpha, http://linkedlifedata.com/resource/pubmed/chemical/Hepatocyte Nuclear Factor 3-beta, http://linkedlifedata.com/resource/pubmed/chemical/Hepatocyte Nuclear Factor 6, http://linkedlifedata.com/resource/pubmed/chemical/Homeodomain Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Hydroxysteroid Dehydrogenases, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Onecut1 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Phosphoenolpyruvate Carboxykinase..., http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/bile acid binding proteins
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0270-9139
pubmed:author
pubmed:issnType
Print
pubmed:volume
35
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
30-9
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:11786957-Adenoviridae, pubmed-meshheading:11786957-Animals, pubmed-meshheading:11786957-Carrier Proteins, pubmed-meshheading:11786957-DNA-Binding Proteins, pubmed-meshheading:11786957-Gene Expression, pubmed-meshheading:11786957-Genetic Vectors, pubmed-meshheading:11786957-Gluconeogenesis, pubmed-meshheading:11786957-Glucose, pubmed-meshheading:11786957-Glucose-6-Phosphatase, pubmed-meshheading:11786957-Glucuronosyltransferase, pubmed-meshheading:11786957-Glycogen, pubmed-meshheading:11786957-Hepatocyte Nuclear Factor 3-alpha, pubmed-meshheading:11786957-Hepatocyte Nuclear Factor 3-beta, pubmed-meshheading:11786957-Hepatocyte Nuclear Factor 6, pubmed-meshheading:11786957-Homeodomain Proteins, pubmed-meshheading:11786957-Homeostasis, pubmed-meshheading:11786957-Hydroxysteroid Dehydrogenases, pubmed-meshheading:11786957-Injections, pubmed-meshheading:11786957-Liver, pubmed-meshheading:11786957-Membrane Glycoproteins, pubmed-meshheading:11786957-Mice, pubmed-meshheading:11786957-Mice, Transgenic, pubmed-meshheading:11786957-Nuclear Proteins, pubmed-meshheading:11786957-Phosphoenolpyruvate Carboxykinase (GTP), pubmed-meshheading:11786957-Tail, pubmed-meshheading:11786957-Trans-Activators, pubmed-meshheading:11786957-Transcription Factors, pubmed-meshheading:11786957-Transfection, pubmed-meshheading:11786957-Veins
pubmed:year
2002
pubmed:articleTitle
Adenovirus-mediated increase in HNF-3beta or HNF-3alpha shows differences in levels of liver glycogen and gene expression.
pubmed:affiliation
University of Illinois at Chicago, College of Medicine, Department of Molecular Genetics, Chicago, IL 60607-7170, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.