Czech J. Anim. Sci., 2008, 53(4):176-179 | DOI: 10.17221/372-CJAS

Mutation in the RPE65 gene causing hereditary retinal dystrophy in the Briard dogs: application of a new detection method

R. Bechyňová1,2, J. Dostál1, A. Stratil1, F. Jílek2, P. Horák1
1 Institute of Animal Physiology and Genetics, v.v.i., Academy of Sciences of the Czech Republic, Liběchov, Czech Republic
2 Department of Veterinary Sciences, Faculty of Agrobiology, Food and Natural Resources, Czech University of Life Sciences in Prague, Prague, Czech Republic

Inherited eye diseases are widespread in most of the pure dog breeds and they show a severe impact on canine health, welfare and working ability. Congenital stationary night blindness (CSNB) was originally described in Briards. CSNB is slow progressive retinal degeneration with very early onset of clinical symptoms and is inherited in an autosomal recessive manner. The causative mutation (Y16567.1:c.487_490delAAGA) for CSNB was identified in exon 5 of the RPE65 gene. This deletion results in a frameshift and leads to a premature stop codon and expression of a non-functional protein. To date, only expensive, laborious or unpractical methods have been used for detection of the mutation in the canine RPE65 gene. The main goals of this study were to develop a new method for routine genotyping of the causative mutation and to assess its occurrence in the Czech population of Briards. The method of electrophoresis in the gel Spraedex EL600 can be widely used for genotyping of the RPE65 gene as a basis of proper genetic counselling and an improvement of genetic health in the Briard populations. In the studied population, the following frequencies of alleles + (wild) and - (mutant) were observed - 0.939 and 0.061, respectively.

Keywords: RPE65 gene; CSNB; dog; Briard; electrophoresis

Published: April 30, 2008  Show citation

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Bechyňová R, Dostál J, Stratil A, Jílek F, Horák P. Mutation in the RPE65 gene causing hereditary retinal dystrophy in the Briard dogs: application of a new detection method. Czech J. Anim. Sci.. 2008;53(4):176-179. doi: 10.17221/372-CJAS.
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References

  1. Aguirre G.D., Baldwin V., Pearce-Kelling S., Narfström K., Ray K., Acland G.M. (1998): Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect. Mol. Vis., 4, 23. Go to PubMed...
  2. Dekomien G., Epplen J.T. (2003): Evaluation of the canine RPE65 gene in affected dogs with generalized progressive retinal atrophy. Mol. Vis., 9, 601-605. Go to PubMed...
  3. Gu S., Thompson D.A., Srikumari C.R.S., Lorenz B., Finckh U., Nicoletti A., Murthy K.R., Rathmann M., Kumaramanickavel G., Denton M.J., Gal A. (1997): Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy. Nat. Genet., 17, 194-197. Go to original source... Go to PubMed...
  4. Kondo H., Qin M., Mizota A., Kondo M., Hayashi H., Hayashi K., Oshima K., Tahira T., Hayashi K. (2004): A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentosa using microsatellite markers. Invest. Ophthalmol. Vis. Sci., 45, 4433-4439. Go to original source... Go to PubMed...
  5. Marlhens F., Bareil C., Griffoin J.M., Zrenner E., Amalric P., Eliaou C., Liu S.Y., Harris E., Redmond T.M., Arnaud B., Claustres M., Hamel C.P. (1997): Mutations in RPE65 cause Leber's congenital amaurosis. Nat. Genet., 17, 139-141. Go to original source... Go to PubMed...
  6. Morimura H., Fishman G.A., Grover S.A., Fulton A.B., Berson E.L., Dryja T.P. (1998): Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis. Proc. Natl. Acad. Sci. USA, 95, 3088-3093. Go to original source... Go to PubMed...
  7. Moise ye v G., Chen Y., Takahashi Y., Wu B.X., Ma J. (2005): RPE65 is the isomerohydrolase in the retinoid visual cycle. Proc. Natl. Acad. Sci. USA, 102, 12413-12418. Go to original source... Go to PubMed...
  8. Narfström K., Wrigstad A., Nilsson S.E. (1989): The Briard dog: A new animal model of congenital stationary night blindness. Brit. J. Ophthalmol., 73, 750-756. Go to original source... Go to PubMed...
  9. Nicoletti A., Wong D.J., Kawase K., Gibson L.H., YangFeng T.L., Richards J.E., Thompson D.A. (1995): Molecular characterization of the human gene encoding an abundant 61 kDa protein specific to the retinal pigment epithelium. Hum. Mol. Genet., 4, 641-649. Go to original source... Go to PubMed...
  10. Switonski M., Konieczny P., Klukowska J., Janyga B., Aguirre G. (2002): Microdeletion in the RPE65 gene causing hereditary retinal dystrophy (HRD) disease segregates in the Polish population of Briards. Med. Weter., 58, 946-949.
  11. Veske A., Nilsson S., Narfström K., Gal A. (1999): Retinal dystrophy of Swedish Briard/Briard-Beagle dogs is due to a 4-bp deletion in RPE65. Genomics, 57, 57-61. Go to original source... Go to PubMed...

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