Genetics and dog breeding Flashcards

1
Q

Most Popular Dog Breeds

A

 Labrador Retrievers (29 years in a row) – data from the American Kennel Club (AKC) so this means ONLY registered breeds and ignores popularity of designer breeds

-then german shepherd, then golden retriever…

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2
Q

can mixed breeds register with AKC?

A

AKC has realized they were losing a huge clientele and you can now register your mutt (or designer breed or whatever) through the AKC Canine PartnersTM Program
 This allows “mutts” to participate in sporting events with their owners

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3
Q

Reasons for Genetic Testing

A

 Paternity
 Disease testing
> Carrier (recessive traits)
> Affected
> Clear
 Trait testing, eg. coat colour testing eg. does this black Lab carry chocolate or yellow? (formerly pedigree analysis)

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4
Q

peternity testing methods

A

 DNA“Fingerprinting”
 BloodTyping
 AKC requirements for Frequently Used Sires (FUS), frozen semen, etc.

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5
Q

types of DNA tests for paternity

A

 Usemarkers
 The AKC used 10 now 14 with gender verification too (MMI)
 Other labs will perform this too
 Ask CKC about which lab results they will accept

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6
Q

AKC DNA Data bank breadth

A

 As of Dec., 2012 the AKC collected over 653,000 DNA profiles from 228 breeds
 In 2017, the top 11 breeds AKC DNA Profiled
> Labrador Retriever; Yorkshire Terrier; German Shepherd Dog; Dachshund; Poodle; Chihuahua; Golden Retriever; Shih Tzu; Pomeranian; Beagle
> These are not the same as the most popular breed list

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7
Q

AKC DNA Profile Program; how does it work and how extensive is it

A

 >709,000 samples have been submitted
voluntary basis and/or to satisfy AKC DNA requirements.
Frequently Used Sires (FUS) Requirement
 >45% of pups registered are from FUS
Some argue this is the biggest problem in purebred dogs

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8
Q

What is the AKC multiple-sured litters requirement?

A

previously, if your bitch had been bred to more than one stud dog, AKC would refuse to register the litter
-often, owners wouldnt know about multiple sires
-test all puppies to determine sires
- now 14 markers and XX vs XY, no ‘unidentifiables’

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9
Q

what is the AKC compliance audit program?

A

-AKC may show up and ask you for DNA samples from your dogs
-when program started, 11% of ‘purebreds’ were not actually
-identifies puppy parentage
-this program only in USA, not canada
>Expect at least 10% of puppies in Canada have wrongly identified parents

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10
Q

how many inherited diseases described in dogs? usually caused by what kind of mutation?

A

350 to 600 inherited diseases described in dogs
precise mode of inheritance known in ~half
-85% caused by a single gene mutation (monogenic disorders)
- 70% single recessive
- 10% polygenic (eg. hip dysplasia)

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11
Q

what can the canine health information center tell you?

A

CHIC site allows you to search by breed or disease - tells you what a breed should be tested for at minimum
>good for client info before they get a dog
>helps with breeding decisions
>open to public

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12
Q

Influence of Single Sire on Genetic Diseases: common problem in doberman

A

Doberman Pinschers and von Willebrand’s Disease

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13
Q

how has DNA testing allowed us to decreased affected animals

A

DNA testing has decreased affected animals by breeding clears to carriers
1997: 30% affected/51% carriers/19% clear 2008: 19% affected/46% carriers/35% clear

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14
Q

Methods of Genetic Testing

A

 Phenotypic tests, eg. CAER (Companion Animal Eye Registry), PennHip, OFA hips, elbows, shoulder, BAER hearing test, etc.
 Metabolic screening eg. urine in MPS VI
 DNA (really only one to test for those diseases that are not apparent at a
young age and best for “carriers”)
 Parental tests with above

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15
Q

classic example of a partially hereditary genetic condition

A

hip dysplasia

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16
Q

difference between a horizontal and vertical pedigree

A

-horizontal only looks at parents, grandparents
- vertical looks at siblings as well, for all generations

> vertical tells you a lot more about what that animal may be carrying
issue is that we rarely have this much information about siblings

17
Q

OFA reccomendations for fair hips; when is a fair dig a good breeding prospect

A

Fair hips may be within normal limits
eg. Fair hips with a strong hip background and >75% of siblings normal is a good breeding prospect
eg. Excellent hips, but with a weak family background and <75% of its siblings normal is a poor breeding prospect

18
Q

OFA’s Recommended Breeding Principles for hip dysplasia

A
  • Breed normals to normals
  • Breed normals with normal ancestry
  • Breed normals from litters (brothers/sisters) with a low incidence of HD
  • Select a sire that produces a low incidence of HD
  • Replace dogs with dogs that are better than the breed average
19
Q

how are hereditary diseases of purebred dogs tracked?

A

 Every breed has a list of diseases, constantly updated
 Breeders ‘know’ what these are and often what lines have them
 Every breed has internet sites with information

20
Q

World Small Animal Veterinary Association (WSAVA); what info does it give you?

A

 Web site searchable by breed, disease or laboratory
>Can be used to find nearest lab or best lab for testing for breed and also names, when known, the gene being tested

21
Q

Samples for DNA Testing

A

 Whole blood in EDTA (lavender top)
 Cheek (buccal) swab with brush
 Dried blood on filter paper

22
Q

what is a wisdom panel?

A

mixed breed analysis by Mars Veterinary
>tells you what breeds are in your dog
- only check EIC and MDR1 disease genes
-cheek swabs

23
Q

what test is available for mutt health?

A

Royal canin genetic health analysis (blood)
- performed by Mars
-

24
Q

limitatins of mutt genetic testing? uses and issues?

A

 Can’t “verify” it’s a purebred since can’t test for EVERY breed, but can be more sure
 Various claims, most ~90% accuracy
 Prices have come down, all use cheek swabs now
 Only two companies as there was an issue of patents
 Those performing both breed and DNA use blood rather than cheek swabs

25
Q

use of fecal DNA detection for dogs

A

-enforce stoop and poop laws

26
Q

should designer breeders (hybrid) do generic testing? do they often do this?

A

 Many do a lot of genetic testing of parents
 Web sites of those producing designer breeds RARELY say
they do genetic testing
 Counsel clients to do their homework before purchasing any dog
 MUST test parents for common genetic diseases PRIOR to breeding
 Use clear parents differently from carrier
 Use common sense, for example, bad heart worse than missing teeth!

27
Q

Types of DNA Tests for Disease

A

Single gene testing
>Clear or Carrier or Affected
ie. Rare false results unless > 1 gene causing same disease (PRA in Chinese Crested)

Linked-marker gene(s) testing
>A or B or C based on frequency of the marker in the population not linked and % recombination reported at the lab,
ie. Subject to Major interpretation!!

28
Q

Counseling Considerations for DNA test and conditions

A

 Type of DNA test used
 Dominant or recessive trait or X-linked
 Genetic pool for the breed
 Certainty of a genetic basis for the congenital/adult disease/condition
 Severity of disease/condition to health/quality of life of the individual
>eg. cryptorchidism vs PRA vs lysosomal storage disease

29
Q

most common veterinary species with genetic defects? what types?

A

canine
 Musculoskeletal most common followed by organs of special sense

30
Q

is a congenital defect always genetic?

A

Congenital defects are often genetic, BUT
Possible Teratogens: medicines, environmental exposures, vaccines, radiation, plants, nutrition, viruses, circulatory disturbance, mechanical factors, aged gametes, aged parents, and UNKNOWN
Karyotype abnormality – maybe hereditary (eg. Robertsonian Translocation) or aged gametes and parents

31
Q

what is the litter effect for generic disorders?

A

Rarely do all fetuses respond to the same degree
Fetal death, infertility, stillbirth, mummification, congenital defects, apparently normal neonates dying shortly after birth, totally normal puppies

32
Q

how do we approach a diagnosis for congenital disorders?

A

History (as available) of similar defects in related dogs
>Problem with teasing out environment from genetics in a “kennel”

Lists of common defects by breed are available
>Cleft palates in Bulldogs and other brachycephalic breeds

Compare defect with reports in other species, eg. humans, cattle
>Need to do complete gross and perhaps further post mortem or workup
>Karyotype analysis
>Internet

History during pregnancy eg. medicines, exposure to teratogens

When exposed eg. palate closes about 5 weeks of gestation

Exposure to other dogs eg. returning from shows or new arrivals

33
Q

what contributes to possible teratogenicity of drugs?

A

 Properties of the drug, eg. metabolism, lipid solubility  Concentration and duration of drug in dam and any
metabolism
 Access to fetuses
 Stage of development at exposure
 Fetal metabolism of drug
 Individual susceptibility
 “Litter effect” – fetuses will not all respond the same- death, resorption, mummification, congenital defects, stillbirth, normal