Deciphering the Evolution of G Protein-Coupled Receptors in Vertebrates
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G protein-coupled receptors (GPCRs) are ancestrally related membrane proteins on cells that mediate the pharmacological effect
of most drugs and neurotransmitters. GPCRs are the largest group of membrane receptor proteins encoded in the human genome.
Using the case study of vertebrate opioid receptors, this chapter introduces an evolutionary approach to understanding pharmacological
selectivity, predicted from sequence analysis, and confirmed by experimental studies. The same approach can be used to examine
receptor function and applies to other families of GPCRs besides the opioid receptor family. Opioid receptors consist of a
family of four closely related proteins expressed in all vertebrates examined. The three types of opioid receptors shown unequivocally
to mediate analgesia in animal models and in humans are the mu
(MOR), delta
(DOR), and kappa
(KOR) opioid receptor proteins. The role of the fourth member of the opioid receptor family, the nociceptin or orphanin FQ
receptor (ORL), in producing analgesia is not as clear. There are now cDNA sequences for all four types of opioid receptors
that are expressed in the brain of six species from three different classes of vertebrates. This chapter presents a comparative
analysis of vertebrate opioid receptors using bioinformatics and data from recent human genome studies. Results indicate that
opioid receptor genes most likely arose by gene duplication, that there appears to be an evolutionary vector of opioid receptor
type divergence in sequence and function, and that the hMOR
gene shows evidence of positive selection or adaptive evolution in Homo sapiens
. Additionally, unlike many typical reviews, this paper highlights the methods used to come to these conclusions.