Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness.

Article Details

Citation

Dryja TP, Berson EL, Rao VR, Oprian DD

Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness.

Nat Genet. 1993 Jul;4(3):280-3.

PubMed ID
8358437 [ View in PubMed
]
Abstract

A number of mutations in the rhodopsin gene have been shown to cause both dominant and recessive retinitis pigmentosa. Here we describe another phenotype associated with a defect in this gene. We discovered a patient with congenital stationary night blindness who carries the missense mutation Ala292Glu. When coupled with 11-cis-retinal in vitro, Ala292Glu rhodopsin is able to activate transducin in a light-dependent manner like wild-type rhodopsin. However, without a chromophore, Ala292Glu opsin anomalously activates transducin. We speculate that the rod dysfunction in this patient is due to an abnormal, continuous activation of transducin by mutant opsin molecules in photoreceptor outer segments.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
RhodopsinP08100Details