Genetically lean mice result from targeted disruption of the RIIβ subunit of protein kinase A

Abstract

CYCLIC AMP is an important second messenger in the coordinated regulation of cellular metabolism. Its effects are mediated by cAMP-dependent protein kinase (PKA), which is assembled from two regulatory (R) and two catalytic (C) subunits. In mice there are four R genes (encoding RIα, RIβ, RIIα, and RIIβ) and two C genes (encoding Cα and Cβ), expressed in tissue-specific patterns. The RIIβ isoform is abundant in brown and white adipose tissue and brain, with limited expression elsewhere. To elucidate its functions, we generated RIIβ knockout mice. Here we report that mutants appear healthy but have markedly diminished white adipose tissue despite normal food intake. They are protected against developing diet-induced obesity and fatty livers. Mutant brown adipose tissue exhibits a compensatory increase in RIα,which almost entirely replaces lost RIIβ, generating an isoform switch. The holoenzyme from mutant adipose tissue binds cAMP more avidly and is more easily activated than wild-type enzyme. This causes induction of uncoupling protein and elevations of metabolic rate and body temperature, contributing to the lean phenotype. Our results demonstrate a role for the RIIβ holoenzyme in regulating energy balance and adiposity.