| Literature DB >> 9603967 |
Abstract
Heterotrimeric G protein-coupled receptors can activate the mitogen-activated protein kinase (MAPK) cascade. Recent studies using pharmacological inhibitors or dominant-negative mutants of signaling molecules have advanced our understanding of the pathways from G protein-coupled receptors to MAPK. However, molecular genetic analysis of these pathways is inadequate in mammalian cells. Here, using the well characterized Gsalpha- and protein kinase A-deficient S49 mouse lymphoma cells, we provide the molecular genetic evidence that Gsalpha is responsible for transducing the beta-adrenergic receptor signal to MAPK in a protein kinase A-dependent pathway involving Rap1 and Raf (but not Ras) molecules.Entities:
Mesh:
Substances:
Year: 1998 PMID: 9603967 DOI: 10.1074/jbc.273.23.14533
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157