Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/8054
Title: Alternative splicing of G protein-coupled receptors: physiology and pathophysiology
Authors: Markovic, Danijela
Challiss, R. A. John
First Published: Oct-2009
Publisher: Springer Verlag
Citation: Cellular and Molecular Life Sciences, 2009, 66 (20), pp. 3337-3352.
Abstract: The G protein-coupled receptors (GPCRs) are a superfamily of transmembrane receptors that have a broad distribution and can collectively recognise a diverse array of ligands. Activation or inhibition of GPCR signalling can affect many (patho)physiological processes, and consequently they are a major target for existing and emerging drug therapies. A common observation has been that the pharmacological, signalling and regulatory properties of GPCRs can differ in a cell- and tissue-specific manner. Such “phenotypic” diversity might be attributable to post-translational modifications and/or association of GPCRs with accessory proteins, however, post-transcriptional mechanisms are also likely to contribute. Although approximately 50% of GPCR genes are intronless, those that possess introns can undergo alternative splicing, generating GPCR subtype isoforms that may differ in their pharmacological, signalling and regulatory properties. In this review we shall highlight recent research into GPCR splice variation and discuss the potential consequences this might have for GPCR function in health and disease.
DOI Link: 10.1007/s00018-009-0093-4
ISSN: 1420-682X
Links: http://link.springer.com/article/10.1007%2Fs00018-009-0093-4
http://hdl.handle.net/2381/8054
Type: Article
Description: This is the author's final draft of the paper published as Cellular and Molecular Life Sciences, 2009, 66 (20), pp. 3337-3352. The original publication is available at www.springerlink.com. Doi: 10.1007/s00018-009-0093-4
Appears in Collections:Published Articles, Dept. of Cell Physiology and Pharmacology

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