Neuron
Volume 9, Issue 4, October 1992, Pages 719-725
Journal home page for Neuron

Article
Constitutively active mutants of rhodopsin

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Abstract

Two critical amino acids in the visual pigment rhodopsin are Lys-296, the site of attachment of retinal to the protein through a protonated Schiff base linkage, and Glu-113, the Schiff base counterion. Mutation of Lys-296 or Glu-113 results in constitutive activation of opsin, as assayed by its ability to activate transducin in the absence of added chromophore. We conclude that opsin is constrained to an inactive conformation by a salt bridge between Lys-296 and Glu-113. Recently, one of the mutants, K296E, was found in a family with retinitis pigmentosa, suggesting that degeneration of the photoreceptor cells in individuals with this mutation may result from persistent stimulation of the phototransduction pathway.

References (42)

  • M. Wessling-Resnick et al.

    Allosteric behavior in transducin activation mediated by rhodopsin

    J. Biol. Chem.

    (1987)
  • L.F. Allen et al.

    G-protein-coupled receptor genes as protooncogenes: constitutively activating mutation of the α1B-adrenergic receptor enhances mitogenesis and tumorigenicity

  • M.L. Applebury

    Insight into blindness

    Nature

    (1990)
  • D. Bownds

    Site of attachment of retinal in rhodopsin

    Nature

    (1967)
  • H.G. Dohlman et al.

    A family of receptors coupled to guanine nucleotide regulatory proteins

    Biochemistry

    (1987)
  • H.G. Dohlman et al.

    Model systems for the study of seven-transmembrane-segment receptors

    Annu. Rev. Biochem.

    (1991)
  • A.G. Doukas et al.

    Resonance Raman studies of bovine metarhodopsin I and metarhodopsin II

    Biochemistry

    (1978)
  • T.P. Dryja et al.

    A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

    Nature

    (1990)
  • T.P. Dryja et al.

    Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa

    N. Engl. J. Med.

    (1990)
  • G.J. Farrar et al.

    Autosomal dominant retinitis pigmentosa: absence of the rhodopsin proline→histidine substitution (codon 23) in pedigrees from Europe

    Am. J. Hum. Genet.

    (1990)
  • L. Ferretti et al.

    Total synthesis of a gene for bovine rhodopsin

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