Dual role of the RIC-3 protein in trafficking of serotonin and nicotinic acetylcholine receptors

Abstract

The ric-3 gene is required for maturation of nicotinic acetylcholine receptors in Caenorhabditis elegans. The human homolog of RIC-3, hRIC-3, enhances expression of α7 nicotinic receptors in Xenopus laevis oocytes, whereas it totally abolishes expression of α4β2 nicotinic and 5-HT3 serotonergic receptors. Both the N-terminal region of hRIC-3, which contains two transmembrane segments, and the C-terminal region are needed for these differential effects. hRIC-3 inhibits receptor expression by hindering export of mature receptors to the cell membrane. By using chimeric proteins made of α7 and 5-HT3 receptors, we have shown that the presence of an extracellular isoleucine close to the first transmembrane receptor fragment is responsible for the transport arrest induced by hRIC-3. Enhancement of α7 receptor expression occurs, at least, at two levels: by increasing the number of mature receptors and facilitating its transport to the membrane. Certain amino acids of a putative amphipathic helix present at the large cytoplasmic region of the α7 subunit are required for these actions. Therefore, hRIC-3 can act as a specific regulator of receptor expression at different levels. © 2005 by The American Society for Biochemistry and Molecular Biology, Inc.