Human peroxisome proliferator activated receptor gamma coactivator 1 (PPARGC1) gene: cDNA sequence, genomic organization, chromosomal localization, and tissue expression.

Abstract

Brown adipose and muscle tissues can increase energy expenditure via adaptive thermogenesis, thereby protecting against obesity. Mouse peroxisome proliferator activated receptor gamma coactivator 1 (Pgc1) has been reported to enhance the expression of uncoupling protein-1, a key mediator of thermogenesis in brown adipose tissue (Puigserver et al., 1998, Cell 92, 829-839). We report here the characterization of the human PPARGC1 gene. PPARGC1 spans a genomic region of approximately 67 kb, is composed of 13 exons, and encodes a 91-kDa protein that exhibits 94% amino acid identity with the mouse ortholog. mRNA species, transcribed from the TATA-less promoter, are 6.4 and 5.3 kb in length due to utilization of two polyadenylation signals. Northern blotting revealed expression of both transcripts in heart, skeletal muscle, and kidney and to a lesser extent in liver, brain, and pancreas as well as in the perirenal adipose tissue of a pheochromocytoma patient. PPARGC1 was mapped to chromosome 4p15.1, a region that has been associated with basal insulin levels in Pima Indians. Hence, PPARGC1 expression might influence insulin sensitivity as well as energy expenditure, thereby contributing to the development and pathophysiology of human obesity.

• Authors: H Esterbauer, H Oberkofler, F Krempler, W Patsch
• Journal: Genomics (Genomics) Vol. 62 Issue 1 Pg. 98-102 (Nov 15 1999) ISSN: 0888-7543 [Print] United States
• PMID: 10585775 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright 1999 Academic Press.

Chemical References

• DNA, Complementary
• RNA, Messenger
• Transcription Factors
• peroxisome-proliferator-activated receptor-gamma coactivator-1

Topics

• Amino Acid Sequence
• Animals
• Binding Sites
• Chromosome Mapping
• Chromosomes, Human, Pair 4 (genetics)
• DNA, Complementary (genetics)
• Energy Metabolism (genetics)
• Exons (genetics)
• Gene Expression Regulation
• Genes
• Genetic Predisposition to Disease
• Humans
• Indians, North American (genetics)
• Insulin Resistance (genetics)
• Mice
• Molecular Sequence Data
• Multigene Family
• Organ Specificity
• Polymerase Chain Reaction
• RNA, Messenger (biosynthesis, genetics)
• Sequence Alignment
• Sequence Homology, Amino Acid
• Transcription Factors (biosynthesis, genetics, metabolism, physiology)