Eliminerende
feil i henhold til rasebekrivelsen for Berner Sennen av FCI.
Dette er ikke ment å sette i gang en debatt - kun informasjon.
I mai 2003 ble
det noen endringer i rasebeskrivelsen når det gjelder eliminerende feil.
Bernere med haleknekk ble
i den nye rasebbeskrivelsen tatt inn som eliminerende feil - medfødt
haleknekk - ved skade bør man få legeattest. Dette hadde i første
omgang konsekvenser for
hunder med haleknekk som ble vist på hundeutstilling. FCI regelverket
sier at hunder med eliminerende feil
i henhold til rasestandard skal/bør ha 0- premie.
I tillegg vil
dette også føre til at hunden ikke/bør kunne godkjennes
som avlshund i henhold til reglene for avl
som gjelder i Norsk Berner Sennenhund Klubb - avlshund må ha oppnådd
I AK på utstilling.
Nå er det jo slik at dommere ikke alltid - noe de skal i henhold til
regelverket for dommerer fra FCI -
har satt seg inn i siste rasebeskrivelse for rasen de skal dømme, senest
dagen før de skal dømme en rase.
Dette medfører at bernere med denne eliminerende feilen vil kunne oppnå
I AK og selvfølgelig være
godkjent avlshund i henhold til norske regler.
Nå er det
vel slik at jeg som tillitsvalgt ikke burde skrive noe om dette på egne
web sider, men synes
likevel at det kan være på sin plass. Jeg har vært en del
opptatt av dette da jeg ikke kan få avlsgodkjent min egen tispe
da hun kun har oppnådd 2AK på utstilling. Regner også med
at det er en del andre - både oppdrettere
og utstillere som er opptatt av slike saker både med hensyn på
avl og utstilling.
Jeg har undersøkt
en god del på nettet og da jeg er medlem av 3 bernergrupper på
nettet
Showberner - NaturalBerner - BernerL
fant jeg ut at
jeg ville forespørre medlemmene i BernerL. Gruppen har 2150 medlemmer
-
både bernereiere og oppdrettere.
Jeg vet ikke i
hvilken grad Pat Long er kjent for norske bernereiere/oppdrettere. Internasjonalt
er han en ganske kjent bernerkjenner som har et ry for å være
meget seriøs. Synes det er viktig
å gjengi hans svar, da det kan være med å oppklare synspunkter
rundt de nye reglene:
"You
mention that the kink in the tail is an eliminating fault. Is
that in the FCI standard? In the AKC standard, a kink is a fault, but not
a
disqualifying fault. The only disqualifying faults we have here is blue eyes
and a ground coat color other than black, or the red coat. So in this
country, it is possible to get a championship on a dog with a kink in the
tail. If the dog happens to be an excellent example of the breed other than
the kink, I would hope the breeder would consider breeding him/her, and go
forward with a puppy from the litter without a kink."
"Du
nevnte at haleknekk er en eliminerende feil. Gjelder det FCI standarden? I
AKC standard (gjelder i USA),
er haleknekk en feil, men ikke en eliminerende feil. De eneste eliminerende
feil vi har er blå øyne
og grunnfarge annen enn svart, eller rød pels. Så i dette landet
vil det være mulig å bli Champion
for en hund med haleknekk. Hvis hunden er et utmerket eksemplar av rasen,
uten andre feil
enn haleknekk, håper jeg at oppdretter vil overveie å bruke han/henne
i avl, og avle videre
fra kullet med en valp uten haleknekk."
Dette svaret
synes jeg er en god grunn til å ta opp saken på egen hjemmeside
- da svaret
er svært opplysende - og ikke minst at det kommer fra en som inngir
autoritet på området
og som bruker svært mye av sin tid på rasen vår og ikke
minst at AKC standarden
ikke har haleknekk som en eliminerende feil.
http://www.akc.org/breeds/bernese_mountain_dog/
http://www.bmdca.org/
http://www.bmdcc.ca/ckc_standard.htm
Man burde derfor få et svar fra FCI hva grunnen er at denne regelen
er kommet
på standarden for berner sennen - har vel aldri vært noe problem
i Norge.
Håper at
dette er opplysende for andre enn bare meg.
Det er viktig å huske på kriteriene han gir for å benytte en hanne/tispe.
HOW ARE DEFECTS INHERITED?
The magic of heredity - DNA, chromosomes, genes
All animals are made up of billions of tiny cells. The nucleus of these cells contains all the information to regulate the activity of the cell and therefore the form and function of the particular body tissue, and ultimately to form the individual animal. This information originally comes from the parents of the animal, with approximately one half from the mother and one half from the father.
This information from which all life develops is in the form of DNA (deoxyribonucleic acid). A gene is a portion of a DNA molecule, carried on a chromosome. Think of a chromosome as a long string of genes. Hundreds and even thousands of genes may be carried on a particular chromosome. Chromosomes occur in pairs in the cell nucleus, except in the egg and sperm where they occur in half pairs. When an egg is fertilized by the sperm, the resulting cell from which the animal will develop has complete pairs again. This is the way in which one half of the genetic information comes from each parent.
The dog has 78 chromosomes, in 39 pairs, on which approximately 100,000 genes are located. This makes up the animal's genotype. The phenotype is what you actually see in the animal, and this can be influenced by both environmental and developmental factors. For example, a dog's size as an adult is determined partly by his or her genes, but is also influenced by environmental factors such as its health as a puppy and the food it eats.
Each gene in a chromosome pair has a partner at the same position (or locus) on the matching chromosome. Each member of a gene pair is called an allele. A gene can have many alleles within a population but an individual animal will have only 2 alleles which influence a particular trait. If the 2 alleles are identical (AA or aa for example), the individual is homozygous at that locus; if the alleles are different (Aa), then heterozygous.
If the allele is dominant, only 1 copy is required to express the trait; if recessive then 2 copies. Upper case letters are traditionally used to represent dominant traits, lower case letters for recessive traits. Thus for a dominant trait, either AA or Aa will express the particular characteristic, while for a recessive trait only aa will express the characteristic. The heterozygote (Aa) will be a carrier - clinically unaffected but able to pass the harmful allele to the offspring.
Example:
Progressive retinal atrophy (PRA) causes blindness in many breeds. P represents the dominant allele, and p the recessive allele. Since PRA is a recessive trait, p is the affected allele, and P the normal allele.
The genotypes PP and pp are homozygous. Dogs with the genotype PP have normal sight and those with pp are affected.
Pp is heterozygous. These animal have normal sight but are carriers. They will pass the allele for progressive retinal atrophy to approximately half their offspring.
Phenotypically, both PP and Pp have normal sight, but their genotype is different. At this time, as with most recessive disorders, there is no way to identify carriers (animals with the genotype Pp) until affected offspring are born.
Sex-linked characteristics are slightly different. Females have a pair of X chromosomes (XX) while males have 1 X and 1 Y chromosome (XY). Thus 1 dose of a recessive X-linked trait (x) will cause the expression of that characteristic in a male, while a female with only 1 dose(Xx) will be a clinically unaffected carrier . The bleeding disorder hemophilia is probably the best known example of a sex-linked condition.
Defects: inherited or not?
A disease condition or abnormality may be caused by many factors. Some of these are genetic; that is the disorder is a result of a mutation in a gene that carries particular information. Some mutations are spontaneous, such as a mutation caused by toxins consumed by the mother during pregnancy. An inherited defect is one in which the defective gene has been inherited from one or both of the parents.
Many conditions that have a well-documented hereditary basis may also have other causes. For example, there are several forms of hereditary cataracts, but cataracts may also occur as a result of injury, toxins, or a disease such as diabetes. In trying to determine whether a disorder is inherited, your veterinarian will look at many factors, including the age the disorder becomes evident, whether littermates or other relatives are affected, and whether the defect is known to occur in that breed. It is very important that inherited disorders be identified so that information can be relayed back to the breeder, and on a larger scale, so that breeding programmes can be designed to reduce or eliminate these debilitating conditions in dogs.
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Patterns of inheritance
The specific pattern of inheritance has not been established for many of the disorders that are believed to be inherited. Where the mode of inheritance is not known, breeds that have an increased risk relative to other dog breeds are said to have a breed predisposition for a particular condition.
The following describes known patterns of inheritance.
Autosomal dominant
Only 1 copy of the gene, which may be inherited from either parent, is required to produce the trait. The parent with the dominant trait will pass the affected gene to approximately half its offspring, and the trait will be apparent in both the parent and the affected progeny. These conditions are uncommon because, as long as it is of early onset (ie becomes apparent before breeding age is reached), the disorder can be readily eliminated by avoiding the breeding of affected individuals.
In many instances however, there is incomplete dominance. The trait may be dominant with variable expressivity, which means that if either parent is affected, all puppies have a susceptibility to the disorder but not all will be affected equally. Alternately, a dominant trait may have incomplete penetrance. If penetrance is 75% for example, only about 3 quarters of the pups who inherit the trait will express it.
Autosomal recessive
This is the most common mode of inheritance for genetic conditions in dogs. Progressive retinal atrophy (PRA), which causes blindness in many breeds, is such a trait. To be affected, the animal must inherit 2 copies of the gene (genotype pp), 1 from each parent. Dogs with the genotype PP (normal) or Pp (carrier) will be clinically normal but the carrier will pass the affected gene to approximately half the offspring. As long as carriers (Pp) are mated to normal animals (PP), the offspring will be unaffected but some will remain carriers. If 2 carriers are mated, some of the offspring (approximately 25%) will be affected.
example:
As long as the frequency of a gene for a recessive disorder remains low in the population, the particular gene may be passed along for many generations before by chance 2 carriers are mated and affected individuals are born. However, the gene frequency may become unusually high due to breeding of close family members, or because of the "popular sire" effect , where a sire with a harmful recessive gene is mated frequently because of desirable traits.
Because the recessive gene is carried in the population in outwardly normal animals, it is very difficult to eradicate these traits. However the incidence can be reduced by identification of carriers through test matings or through various tests that have been developed, and the conscientious use of this information in breeding programmes. Veterinarians, dog breeders, and breed associations must all work together for substantial progress to be achieved.
Sex-linked traits
In these traits, the gene is located on the X chromosome. Males have 1 X chromosome from their mother, and 1 Y chromosome from their father, which carries little information other than maleness. Females have 2 X chromosomes, 1 each from their mother and father. So if a mother who is a carrier for a harmful recessive gene (Xx) passes the recessive gene (x) to her daughter, the daughter will be an unaffected carrier, but her sons who receive that gene will be affected.
The bleeding disorder hemophilia is the best known of the X-linked traits, which are uncommon in the dog. Control programmes are possible because carrier females can be identified through blood screening.
The above-mentioned traits are inherited in a straightforward manner. Many others are inherited in a more complex fashion. In fact, most traits that are selected for in the dog are the result of the interaction of many genes. Modifying genes may influence how other genes are expressed. As mentioned above, a trait may be dominant, but with incomplete penetrance so that it is not always expressed. Epistaxis occurs when alleles at one locus mask the action of another pair of alleles.
Polygenic inheritance
Polygenic traits are controlled by an unknown number of genes. The gene expression is influenced by a variety of factors including gender, nutrition, breed, rate of growth, and amount of exercise. These traits are quantitative traits - that is, there is a wide range within the population. Such traits include height, weight, character, working abilities, and some genetic defects. Heritability varies within different breeds and within different populations of a particular breed.
Because it is virtually impossible to determine the exact genotype for such traits, it is difficult to control defects with a polygenic mode of inheritance. The best attempts at control are based on a grading scheme for identification of the defect and a breed policy of recording and publishing the results for as many dogs as possible. Canine hip dysplasia is a polygenic trait that remains a problem in most large breeds of dog, despite efforts to control this condition dating back to the 1960s. Breed organizations and veterinarians in various countries have developed control programmes that rely on radiographic evaluation and a central registry of dogs. Thoughtful selection by breeders, using this information, has greatly reduced the incidence of hip dysplasia in those breeds in particular countries.
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This database is funded jointly by the Animal Welfare Unit at the Atlantic Veterinary College, University of Prince Edward Island, and the Canadian Veterinary Medical Association.
Copyright © 1998 Canine Inherited Disorders Database. All rights reserved.
Revised: December 15, 2000.
Ellers er det en veldig interessant side for oss som
lurer litt på
hva kritikkene på utstilling betyr og som kan gi oss litt bedre
forståelse for å vurdere egen berner:
Se Illustrated standard 2006
http://www.berneru.org