Abstract
G-protein-linked receptors constitute a populous family of heptahelical, membrane-localized receptors for hormones, drugs and neurotransmitters that activate a diverse and smaller subset of effectors, including adenylylcyclases, phospholipases and various ion channels. The expression and functional status of G-protein-linked receptors is highly regulated. Expression is controlled largely by activation or repression of the genes encoding the receptors, balanced by post-transcriptional mechanisms such as destabilization of receptor mRNA. Agonist-induced down-regulation of receptors involves both transcriptional and post-transcriptional controls. Gene structure reveals details of promoters as well as determinants for mRNA stability. Post-translational regulation of G-protein-linked receptors is dominated by protein phosphorylation. G-protein-linked receptors are substrates not only for protein kinase A, protein kinase C and receptor-specific kinases, but also for growth factor receptors with intrinsic tyrosine kinase activity. Recent advances in the study of β-adrenergic receptors (βARs) illuminate new dynamic features of receptor regulation, central to our understanding of neurobiology.
| Original language | English |
|---|---|
| Pages (from-to) | 555-568 |
| Number of pages | 14 |
| Journal | Progress in Neurobiology |
| Volume | 48 |
| Issue number | 6 |
| DOIs | |
| State | Published - Apr 1996 |
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