Inheritance of cataracts and primary lens luxation in Jack Russell Terriers

Anita M. Oberbauer Department of Animal Science, College of Agricultural and Environmental Sciences, University of California, Davis, CA 95616.

Search for other papers by Anita M. Oberbauer in
Current site
Google Scholar
PubMed
Close
 PhD
,
Steven R. Hollingsworth Department of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California, Davis, CA 95616.

Search for other papers by Steven R. Hollingsworth in
Current site
Google Scholar
PubMed
Close
 DVM
,
Janelle M. Belanger Department of Animal Science, College of Agricultural and Environmental Sciences, University of California, Davis, CA 95616.

Search for other papers by Janelle M. Belanger in
Current site
Google Scholar
PubMed
Close
 MS
,
Kelly R. Regan Department of Animal Science, College of Agricultural and Environmental Sciences, University of California, Davis, CA 95616.

Search for other papers by Kelly R. Regan in
Current site
Google Scholar
PubMed
Close
 BS
, and
Thomas R. Famula Department of Animal Science, College of Agricultural and Environmental Sciences, University of California, Davis, CA 95616.

Search for other papers by Thomas R. Famula in
Current site
Google Scholar
PubMed
Close
 PhD

Abstract

Objective—To characterize heritability and mode of inheritance of cataracts and primary lens luxation in Jack Russell Terriers.

Animals—872 Jack Russell Terriers from which buccal epithelial cells were collected and phenotypes for cataracts and lens luxation were determined and an additional 1,898 Jack Russell Terriers without phenotypic information used to complete pedigree relationships and that were included in the analyses.

Procedures—Narrow-sense heritabilities and genetic correlation for cataracts and lens luxation were modeled by use of threshold analysis, whereas complex segregation analysis was used to characterize mode of inheritance. For the analyses, dogs < 6 years old, unless confirmed as having cataracts or lens luxation, were classified as an unknown phenotype. The possible involvement of an HSF4 mutation in cataracts was determined by DNA sequencing.

Results—Cataracts and primary lens luxation were highly heritable and genetically correlated, and neither was controlled by a single gene. Cataracts were not associated with an HSF4 mutation.

Conclusions and Clinical Relevance—Analysis of the data indicated that concerted selection against both cataracts and primary lens luxation when choosing breeding animals can be used to improve ocular health in Jack Russell Terriers.

Abstract

Objective—To characterize heritability and mode of inheritance of cataracts and primary lens luxation in Jack Russell Terriers.

Animals—872 Jack Russell Terriers from which buccal epithelial cells were collected and phenotypes for cataracts and lens luxation were determined and an additional 1,898 Jack Russell Terriers without phenotypic information used to complete pedigree relationships and that were included in the analyses.

Procedures—Narrow-sense heritabilities and genetic correlation for cataracts and lens luxation were modeled by use of threshold analysis, whereas complex segregation analysis was used to characterize mode of inheritance. For the analyses, dogs < 6 years old, unless confirmed as having cataracts or lens luxation, were classified as an unknown phenotype. The possible involvement of an HSF4 mutation in cataracts was determined by DNA sequencing.

Results—Cataracts and primary lens luxation were highly heritable and genetically correlated, and neither was controlled by a single gene. Cataracts were not associated with an HSF4 mutation.

Conclusions and Clinical Relevance—Analysis of the data indicated that concerted selection against both cataracts and primary lens luxation when choosing breeding animals can be used to improve ocular health in Jack Russell Terriers.

Contributor Notes

Supported by the American Kennel Club Canine Health Foundation (grant Nos. 2228 and 0351).

The authors thank Dr. L. Janss for technical assistance with the computer software.

Address correspondence to Dr. Oberbauer.
  • 1.

    Gelatt KN, MacKay EO. Prevalence of primary breed-related cataracts in the dog in North America. Vet Ophthalmol 2005;8:101111.

  • 2.

    Davidson MG, Nelms SR. Diseases of the lens and cataract formation. In: Gelatt KN, ed. Veterinary ophthalmology. 3rd ed. Philadelphia: Lippincott Williams & Wilkins, 1999;797825.

    • Search Google Scholar
    • Export Citation
  • 3.

    Rubin LF. Inherited eye diseases in purebred dogs. Baltimore: Williams & Wilkins, 1989.

  • 4.

    Barnett KC. Comparative aspects of canine hereditary eye disease. Adv Vet Sci Comp Med 1976;20:3967.

  • 5.

    Heinrich CL, Lakhani KH, Featherstone HJ, et al. Cataract in the UK Leonberger population. Vet Ophthalmol 2006;9:350356.

  • 6.

    Wallace MR, MacKay EO, Gelatt KN, et al. Inheritance of cataract in the Bichon Frise. Vet Ophthalmol 2005;8:203205.

  • 7.

    Rubin LF, Koch SA, Huber RJ. Hereditary cataracts in miniature schnauzers. J Am Vet Med Assoc 1969;154:14561458.

  • 8.

    Mellersh CS, Pettitt L, Forman OP, et al. Identification of mutations in HSF4 in dogs of three different breeds with hereditary cataracts. Vet Ophthalmol 2006;9:369378.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 9.

    Davidson MG, Nasisse MP, Rusnak IM, et al. Success rates of unilateral vs. bilateral cataract extraction in dogs. Vet Surg 1990;19:232236.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 10.

    Lannek EB, Miller PE. Development of glaucoma after phacoemulsification for removal of cataracts in dogs: 22 cases (1987–1997). J Am Vet Med Assoc 2001;218:7076.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 11.

    Sidjanin DJ, McElwee J, Miller B, et al. Cloning of canine galactokinase (GALK1) and evaluation as a candidate gene for hereditary cataracts in Labrador retrievers. Anim Genet 2005;36:265266.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 12.

    Hunter LS, Sidjanin DJ, Johnson JL, et al. Radiation hybrid mapping of cataract genes in the dog. Mol Vis 2006;12:588596.

  • 13.

    Kecova H, Necas A. Phacoemulsification and intraocular lens implantation: recent trends in cataract surgery. Acta Veterinaria Brno 2004;73:8592.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 14.

    Lazarus JA, Pickett JP, Champagne ES. Primary lens luxation in the Chinese Shar Pei: clinical and hereditary characteristics. Vet Ophthalmol 1998;1:101107.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 15.

    Nasisse MP, Glover TL. Surgery for lens instability. Vet Clin North Am Small Anim Pract 1997;27:11751192.

  • 16.

    Ketteritzsch K, Hamann H, Brahm R, et al. Genetic analysis of presumed inherited eye diseases in Tibetan Terriers. Vet J 2004;168:151159.

  • 17.

    Willis MB, Curtis R, Barnett KC, et al. Genetic aspects of lens luxation in the Tibetan Terrier. Vet Rec 1979;104:409412.

  • 18.

    Curtis R, Barnett KC, Lewis SJ. Clinical and pathological observations concerning the aetiology of primary lens luxation in the dog. Vet Rec 1983;112:238246.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 19.

    Curtis R, Barnett KC, Startup FG. Primary lens luxation in the Miniature Bull Terrier. Vet Rec 1983;112:328329.

  • 20.

    Curtis R, Barnett KC. Primary lens luxation in the dog. J Small Anim Pract 1980;21:657668.

  • 21.

    Padgett GA. Brief definitions of canine genetic disorders with affected breeds. In: Control of canine genetic diseases. New York: Howell Book House, 1998;219250.

    • Search Google Scholar
    • Export Citation
  • 22.

    Oberbauer AM, Grossman DI, Eggleston ML, et al. Alternatives to blood as a source of DNA for large-scale scanning studies of canine genome linkages. Vet Res Commun 2003;27:2738.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 23.

    Duggirala R, Williams JT, Williams-Blangero S, et al. A variance component approach to dichotomous trait linkage analysis using a threshold model. Genet Epidemiol 1997;14:987992.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 24.

    Bonney GE. Regressive logistic models for familial disease and other binary traits. Biometrics 1986;42:611625.

  • 25.

    Elston RC, Nasmboodrii KK, Glueck CJ, et al. Studies of the genetic transmission of hypercholesterolemia and hypertriglyceridemia in a 195 member kindred. Ann Hum Genet 1975;39:6787.

    • Crossref
    • Search Google Scholar
    • Export Citation
  • 26.

    Janss LLG. MaGGic: a package of subroutines for genetic analyses with Gibbs sampling, in Proceedings. 6th World Cong Genet Appl Livestock Prod 1998;459460.

    • Search Google Scholar
    • Export Citation
  • 27.

    Ensembl's canine genome sequence. Available at: www.ensembl.org/Canis_familiaris/index.html. Accessed Mar 12, 2007.

  • 28.

    Collins BK, Collier LL, Johnson GS, et al. Familial cataracts and concurrent ocular anomalies in chow chows. J Am Vet Med Assoc 1992;200:14851491.

    • Search Google Scholar
    • Export Citation
  • 29.

    Gelatt KN, Samuelson DA, Bauer JE, et al. Inheritance of congenital cataracts and microphthalmia in the Miniature Schnauzer. Am J Vet Res 1983;44:11301132.

    • Search Google Scholar
    • Export Citation
  • 30.

    Laratta LJ, Riis RC, Kern TJ, et al. Multiple congenital ocular defects in the Akita dog. Cornell Vet 1985;75:381392.

  • 31.

    Bettencourt A. Boston Terrier. Kennel Club dog breed series. Allenhurst, NJ: Kennel Club Books, 2003.

  • 32.

    Frome JH. Staffordshire Bull Terrier. Kennel Club dog breed series. Allenhurst, NJ: Kennel Club Books, 2004.

  • 33.

    Pettersall C. Parson Russell Terrier. Kennel Club dog breed series. Allenhurst, NJ: Kennel Club Books, 2003.

  • 34.

    Ostrander EA, Wayne RK. The canine genome. Genome Res 2005;15:17061716.

Advertisement