Cloning and mRNA tissue distribution of human PPAR gamma coactivator-1

Citation
D. Larrouy et al., Cloning and mRNA tissue distribution of human PPAR gamma coactivator-1, INT J OBES, 23(12), 1999, pp. 1327-1332
Citations number
33
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
INTERNATIONAL JOURNAL OF OBESITY
ISSN journal
03070565 → ACNP
Volume
23
Issue
12
Year of publication
1999
Pages
1327 - 1332
Database
ISI
SICI code
0307-0565(199912)23:12<1327:CAMTDO>2.0.ZU;2-X
Abstract
OBJECTIVES: To determine human PPAR gamma coactivator-1 (PGC-1) amino acid sequence and to study PGC-1 mRNA tissue distribution. PGC-1 is a novel tran scriptional coactivator of nuclear receptors that may play a role in the co ntrol of thermogenesis. SUBJECTS: Subcutaneous adipose tissue was obtained from six obese and five lean male subjects. Vastus lateralis skeletal muscle was obtained from seve n lean and six obese subjects undergoing a 5-day severe calorie restriction . Other tissue biopsies were from nonobese nondiabetic subjects. METHODS: Human PGC-1 was cloned from a skeletal muscle cDNA library. A reve rse transcription-competitive polymerase chain reaction assay was developed to determine PGC-1 mRNA levels in human tissues. RESULTS: The human amino acid sequence showed 95% identity with mouse PGC-1 , PGC-1 mRNA was expressed at very low levels in the small and large intest ines and white adipose tissue. Heart, kidney, liver and skeletal muscle sho wed higher mRNA levels. The degree of obesity did not affect PGC-1 mRNA lev els in adipose tissue while lean subjects expressed more PGC-1 mRNA than ob ese subjects in skeletal muscle. A 5-day severe calorie restriction induced PGC-1 mRNA expression in skeletal muscle of obese but not of lean subjects . CONCLUSION: PGC-1 shows a restricted tissue expression that suggests a tiss ue-specific role in the control of gene transcription and possible interact ion with various members of the PPAR family. The lower expression of skelet al muscle PGC-1 in obesity could contribute to an alteration of mitochondri al gene expression.