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Written by: Jeff Vidt, DVM


Genetic Tests

Fueled by the explosive advancements in biology, genetics, biochemistry, molecular biology and technology we have entered a time of significant advances in the study of genetic diseases in dogs. The completion of the Canine Genome Project will only accelerate our understanding in this area. Key to the practical usage of knowledge in the field of canine genetic diseases is the development and application of DNA-based genetic tests. DNA-based genetic tests identify differences in DNA sequences and are of two different types. The mutation-based test recognizes disease-causing mutations while the linked polymorphism test recognizes DNA differences that are near the disease-causing gene and are used to track both normal and mutant alleles of that gene through pedigrees. An allele is an alternative form of a gene inherited from each parent. There are differences in how these two tests are developed and used but both involve the same basic techniques. The most powerful tool developed in the last 10 years or so is the polymerase chain reaction (PCR). By the use of this tool millions of copies of the same DNA sequence can be produced resulting in amplification and the ability to allow rapid genotyping of marker alleles from minute amounts of genomic DNA. A rough analogy would be to take a swab of an infected ear and grow the organism on an agar plate so the organism can be identified and other tests could be done on the larger sample.
  1. Mutation-based tests recognize the specific DNA mutation that causes the genetic disease. These tests:
    1. require knowledge of the specific mutation (which requires that the normal gene sequence is known).
    2. can be used for carrier detection as well as detection of affected animals.
    3. may be breed specific, so different tests may be necessary to test for the same disease in different breeds.
    4. do not require DNA samples from additional members of a pedigree.
  2. Linked polymorphism tests recognize variations in DNA sequence outside but closely linked to the gene involved in the disease. This type of test:
    1. requires the identification of a specific polymorphism or variation in DNA sequence near a disease-causing gene and that is linked with that gene. This means that the they are inherited together. DNA from many individuals within pedigrees in which the disease appears is necessary. However it is not necessary to know the exact mutation, or even the disease-causing gene.
    2. is most accurate for use in families in which the parents of the animal in question are heterozygous (have two different alleles) at the linked marker focus and DNA is available from an affected full sibling of the animal to be tested.
    3. will be in error a small proportion of the time. An error occurs when there is recombination between the linked polymorphic locus and the disease-causing gene. The closer the two genes are, the less chance for recombination to occur and the smaller the degree of error.

Genetic tests in general should: How useful and how successful a genetic screening program depends on the following requisites: The role of veterinary medicine in genetic screening programs includes: The role of the breed club includes: Below is a listing of currently available genetic tests and informative web sites:

Currently Available Genetic Tests

View List (updated)