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• W2101255369 abstract "G protein-coupled receptors (GPCRs) accommodate a wide spectrum of activators from ions to glycoprotein hormones. The mechanism of activation for this large and clinically important family of receptors is poorly understood. Although initially thought to function as monomers, there is a growing body of evidence that GPCR dimers form, and in some cases that these dimers are essential for signal transduction. Here we describe a novel mechanism of intermolecular GPCR activation, which we refer to as trans-activation, in the LH receptor, a GPCR that does not form stable dimers. The LH receptor consists of a 350-amino acid amino-terminal domain, which is responsible for high-affinity binding to human CG, followed by seven-transmembrane domains and connecting loops. This seven-transmembrane domain bundle transmits the signal from the extracellular amino terminus to intracellular G proteins and adenylyl cyclase. Here, we show that binding of hormone to one receptor can activate adenylyl cyclase through its transmembrane bundle, intramolecular activation (cis-activation), as well as trans-activation through the transmembrane bundle of an adjacent receptor, without forming a stable receptor dimer. Coexpression of a mutant receptor defective in hormone binding and another mutant defective in signal generation rescues hormone-activated cAMP production. Our observations provide new insights into the mechanism of receptor activation mechanisms and have implications for the treatment of inherited disorders of glycoprotein hormone receptors." @default.
• W2101255369 created "2016-06-24" @default.
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• W2101255369 date "2002-06-01" @default.
• W2101255369 modified "2023-09-24" @default.
• W2101255369 title "Cis- and Trans-Activation of Hormone Receptors: the LH Receptor" @default.
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• W2101255369 doi "https://doi.org/10.1210/mend.16.6.0852" @default.
• W2101255369 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/12040016" @default.
• W2101255369 hasPublicationYear "2002" @default.
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