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Gene ; 329: 71-9, 2004 Mar 31.
Article in English | MEDLINE | ID: mdl-15033530

ABSTRACT

The chipmunk hibernation-specific protein HP-55 is a component of a 140-kDa complex whose levels are drastically decreased in the blood during hibernation. It is highly homologous to alpha(1)-antitrypsin (AT). In the chipmunk, several alpha(1)-AT-like genes in addition to HP-55 (or CM55-ML) are expressed in the liver and have distinct patterns of regulation during hibernation: in hibernating chipmunks, the level of CM55-ML gene expression is greatly reduced, that of the CM55-MS gene is slightly increased, and the expression of the CM55-MM gene is hardly affected. As a first step towards understanding the hibernation-associated gene regulation of these chipmunk alpha(1)-AT-like genes, we isolated genomic clones for the CM55-ML, CM55-MM, and CM55-MS genes, and analyzed their promoter activities. These alpha(1)-AT-like genes are composed of five exons, and show a similar gene structure to that of the human alpha(1)-AT gene, suggesting that they were generated by the duplication of an ancestral alpha(1)-AT gene. Transient transfection studies using HepG2 and COS-7 cells revealed that for all three alpha(1)-AT-like genes, approximately 150-bp 5' flanking sequences were sufficient for the liver-specific promoter activity, and that the binding of HNF-1 to the promoter region could transactivate transcription. In addition, analysis of the activity of chimeric promoters composed of CM55-ML and CM55-MS gene sequences indicated that the lack of a TATA box-like sequence in the CM55-MS gene is responsible for its weak promoter activity.


Subject(s)
Genes/genetics , Promoter Regions, Genetic/genetics , Sciuridae/genetics , alpha 1-Antitrypsin/genetics , 5' Flanking Region/genetics , Amino Acid Sequence , Animals , Base Sequence , Binding Sites/genetics , COS Cells , Cell Line, Tumor , Chlorocebus aethiops , DNA/chemistry , DNA/genetics , DNA/isolation & purification , DNA-Binding Proteins/metabolism , Exons , Hepatocyte Nuclear Factor 1 , Hepatocyte Nuclear Factor 1-alpha , Humans , Introns , Luciferases/genetics , Luciferases/metabolism , Molecular Sequence Data , Nuclear Proteins/metabolism , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Sequence Analysis, DNA , Transcription Factors/metabolism , Transcription Initiation Site , Transcription, Genetic , Transfection
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