Isoform-specific increases in murine skeletal muscle peroxisome proliferator-activated receptor-γ coactivator-1α (PGC-1α) mRNA in response to β2-adrenergic receptor activation and exercise

Abstract

Adrenergic receptor (AR) activation increases expression of peroxisome proliferator-activated receptor (PPAR)-γ coactivator 1α(PGC- 1α) mRNA, which may promote mitochondrial biogenesis in skeletal muscles. An AR-activated increase in PGC-1α mRNA was observed in exercise. PGC-1α mRNA is considered a single transcript (PGC-1α-a); however, a transcript search of PGC-1α in expressed sequence tag libraries revealed that two novel isoforms of PGC-1α mRNA, named PGC-1α-b and PGC-1α-c, were expressed in mice tissues. Compared with PGC-1α-a mRNA (a previously described isoform), PGC-1α-b or PGC-1α-c mRNA was transcribed by a different exon 1 of the PGC-1αgene and produced slightly smaller-sized proteins. PGC-1α-b or PGC-1α-c protein was functional; both isoforms possessed transcriptional activity and could coactivate PPARs, similar to those in PGC-1α-a in vitro. Transgenic mice overexpressing PGC-1α-b or PGC-1α-c in skeletal muscles showed increased gene expression related to mitochondrial biogenesis and fatty acid oxidation. In C57BL/6J mice, injection of the β2-AR agonist clenbuterol increased PGC-1α-b and PGC-1α-c mRNA expression more than 350-fold, but not PGC-1α-a, in skeletal muscle. A single bout of exercise also increased PGC-1α-b and PGC-1α-c mRNAs, but not PGC-1α-a, in skeletal muscles. The increases in skeletal muscles in response to exercise were inhibited by pretreatment with the β2-AR-specific inhibitor ICI 118,551. However, in liver, fasting increased PGC-1α-a mRNA, but not PGC-1α-b and PGC-1α-c mRNAs. These data indicate that AR activation is a major mechanism of an increase in PGC-1α expression in skeletal muscles, and the increase in PGC-1α mRNAs was isoform specific. Copyright © 2008 by The Endocrine Society.