Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase β-subunit gene

Academic Article


  • Irish setter dogs affected with a rod/cone dysplasia (locus designation, rcd1) display markedly elevated levels of retinal cGMP during postnatal development. The photoreceptor degeneration commences ≃25 days after birth and culminates at about 1 year when the population of rods and cones is depleted. A histone-sensitive retinal cGMP phosphodiesterase (PDE; EC activity, a marker for photoreceptor PDEs, was shown previously to be present in retinal homogenates of immature, affected Irish setters. Here we report that, as judged by HPLC separation, this activity originates exclusively from cone photoreceptors, whereas rod PDE activity is absent. An immunoreactive product the size of the PDE α subunit, but none the size of the β subunit, can be detected on immunoblots of retinal extracts of affected dogs, suggesting a null mutation in the PDE β-subunit gene. Using PCR amplification of Irish setter retinal cDNA, we determined the complete coding sequence of the PDE β subunit in heterozygous and affected animals. The affected PDE β-subunit mRNA contained a nonsense amber mutation at codon 807 (a G → A transition converting TGG to TAG), which was confirmed to be present in putative exon 21 of the affected β-subunit gene. The premature stop codon truncates the β subunit by 49 residues, thus removing the C- terminal domain that is required for posttranslational processing and membrane association. These results suggest that the rcd1 gene encodes the rod photoreceptor PDE β subunit and that a nonsense mutation in this gene is responsible for the production of a nonfunctional rod PDE and the photoreceptor degeneration in the rcd1/rcd1 Irish setter dogs.
  • Authors

    Digital Object Identifier (doi)

    Author List

  • Suber ML; Pittler SJ; Qin N; Wright GC; Holcombe V; Lee RH; Craft CM; Lolley RN; Baehr W; Hurwitz RL
  • Start Page

  • 3968
  • End Page

  • 3972
  • Volume

  • 90
  • Issue

  • 9