regulator of G-protein signaling 9 (RGS9)
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Function
- inhibits signal transduction by increasing GTPase activity of G-alpha subunits thus increasing the amount of inactive GDP-bound form
- binds to Gt-alpha
- role in phototransduction recovery phase (putative)
- retinal isoform 3 is light-dependent phosphorylated at Ser-478
- phosphorylation is decreased by light exposition
- heterodimer with Gbeta5
- interacts with RGS9BP, regulating the subcellular location RGS9/Gbeta5 heterodimer
- component of the RGS9-1-Gbeta5 complex composed of isoform 3 of RGS9 (RGS9-1), Gbeta5 (GNB5) & RGS9BP (probable)
Structure
- in photoreceptor cells the DEP domain is essential for targeting RGS9 to the outer rod segments
- contains 1 DEP domain
- contains 1 G protein gamma domain
- contains 1 RGS domain
Compartment
- isoform 3: membrane; peripheral membrane protein.
- isoform 3 is targeted to the membrane via its interaction with RGS9BP (putative)
Alternative splicing
named isoforms=5
Expression
- highly expressed in the caudate & putamen,
- lower levels found in the hypothalamus & nucleus accumbens
- very low levels in cerebellum
- not expressed in globus pallidus or cingulate cortex
- isoform 2 is expressed predominantly in pineal gland & retina
- isoform 3 is expressed in retina (abundant in photoreceptors)
Pathology
- defects in RGS9 are a cause of prolonged electroretinal response suppression (bradyopsia)