Abstract
The nuclear receptor peroxisome proliferator-activated receptor γ regulates adipose differentiation and systemic insulin signaling via ligand-dependent transcriptional activation of target genes. However, the identities of the biologically relevant target genes are largely unknown. Here we describe the isolation and characterization of a novel target gene induced by PPARγ ligands, termed PGAR (for PPARγ angiopoietin related), which encodes a novel member of the angiopoietin family of secreted proteins. The transcriptional induction of PGAR follows a rapid time course typical of immediate-early genes and occurs in the absence of protein synthesis. The expression of PGAR is predominantly localized to adipose tissues and placenta and is consistently elevated in genetic models of obesity. Hormone-dependent adipocyte differentiation coincides with a dramatic early induction of the PGAR transcript. Alterations in nutrition and leptin administration are found to modulate the PGAR expression in vivo. Taken together, these data suggest a possible role for PGAR in the regulation of systemic lipid metabolism or glucose homeostasis.
ACKNOWLEDGMENTS
We thank C. Walkey for providing tissue samples from animals subjected to fasting-refeeding protocols. We are also grateful to the members of the Spiegelman laboratory for helpful discussions, P. Puigserver for critical comments on the manuscript, and A. Troy for technical assistance.
This work was funded by a grant from the National Institutes of Health (DK31405 to B.M.S.). J.C.Y. is an NIH predoctoral trainee.