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Deafness and the Merle
Gene
George M. Strain, PhD
Professor of Neuroscience
Louisiana State University,
Baton Rouge, LA
Of all the
domestic species, the canine has the greatest variation in size, shape, and skin
pigmentation pattern.1 Results from classical genetic studies in the
last century identified at least ten genetic loci that determine coat color and
pattern, represented by the letters A, B, C, D, E, G, M, P, S, and T.2
Two of these genes, S (piebald) and M (merle), have been linked to the
appearance of congenital hereditary deafness. The S series has one dominant and
three recessive alleles: the dominant S allele produces a solid coat
color, while the recessive alleles si (Irish spotting), sp
(piebald), and sw (extreme piebald) produce increasing amounts
of white in the coat and skin. The Dalmatian breed is homozygous for sw
and is the breed with the highest prevalence of deafness: 30% are deaf in one or
both ears. Other breeds carrying recessive piebald alleles with deafness
problems include the bull terrier, English setter, English cocker spaniel,
Australian cattle dog, and Jack Russell terrier.
The second
pigmentation gene associated with deafness is merle. The dominant allele M
acts on uniform pigmentation to produces an alternating pattern of dark versus
light that is also known as dapple. The recessive allele produces uniform
pigmentation when the dog is homozygous (mm). Heterozygous merle (mM)
in an otherwise black dog produces a blue merle, and in an otherwise brown dog
produces a red merle. Dogs homozygous for the dominant allele (MM) can be
mildly affected to the naked eye or severely affected, depending on breed and
even varying within a breed. Severely affected MM individuals are often
nearly all white, deaf, sterile, and blind or affected by various visual
abnormalities. Merles are commonly seen in the collie, border collie, Australian
shepherd, Shetland sheepdog, Cardigan Welsh corgi, dachshund, and Great Dane
breeds; other breeds less commonly known to carry merle are the Chihuahua,
American pit bull terrier, American Staffordshire terrier, Beauceron, Catahoula
leopard dog, Koolie, poodle, Pyrenean shepherd, Old English sheepdog, American
cocker spaniel, Pomeranian, Hungarian Mudi, Norwegian dunkerhound, and others.
Many of the
breeds that carry merle also carry piebald. Whether it linked to S, M,
or other causes, congenital deafness has been identified in nearly 90 breeds,3
nearly all of which carry piebald, merle, or both. While we know that the
piebald gene is inherited as a simple recessive and the merle gene as a simple
dominant, the inheritance of deafness resulting from either gene does not appear
to be inherited in a simple Mendelian manner – I’ve bred deaf Dalmatian to deaf
Dalmatian and gotten bilaterally hearing puppies. Our data analyses suggest that
the inheritance involves more than one gene: M or s and another
gene that modifies how strongly the first gene acts.
Relatively few
studies of the merle gene have been published, most coming from studies of a
breeding colony of merle dachshunds kept at a university in Hanover, Germany.
One study4 examined auditory function in the animals, and several
(e.g. reference 5) examined visual function. From these limited studies of an
inbred population in one breed, subsequent authors have, unfortunately,
extrapolated the reported findings to apply to all merle-carrying breeds.
Current work in our and other laboratories and the experiences of many breeders
have shown that the actions of merle have usually been over-stated. Reetz et al.4
reported hearing results for 38 dachshunds (Tekels in German): 11 double merles,
19 single merles, and 8 non-merles. They found hearing loss – slight to total,
unilateral or bilateral – in 54.6% of double merles, in 36.8% of single merles,
and in none of the non-merles. Hearing was tested using the brainstem auditory
evoked response (BAER), determining the threshold to click stimuli under
sedation. Any threshold above 20 dB was considered to be abnormal, not because
that is an accepted standard, but because one of their non-merle dogs had a 20
dB hearing threshold. Only one dog – a double merle male – was totally deaf in
both ears (threshold > 90 dB) and none of the dogs were totally deaf in only one
ear (unilaterally deaf). Looked at this way, true bilateral deafness occurred in
9.1% (1/11) of the double merles and 0% of the single merles.
How can the
reported hearing loss in the remaining single and double merles be explained?
The pigment-associated deafness seen with the piebald and merle patterns
typically presents as total deafness in one or both ears, based on all of
the histological studies that have been reported, so the partial hearing loss
reported by Reetz is not likely to be genetic and associated with the merle
gene. Instead, it most likely reflects a combination of poor aural hygiene
(dirty ear canals), middle ear infections, and noise-induced hearing trauma. The
noise level in institutional kennels is notoriously high, and exposure to high
noise levels produces cumulative hearing loss. Dogs in large kennels also
usually do not receive regular ear cleaning, leading to build up of excess
cerumen and infections, both of which muffle the sound reaching the inner ear.
Interestingly, of the 15 “hearing impaired” ears with thresholds between 25 and
50 dB, only 3 were in males. Perhaps differences in kennel housing for females
exposed them to greater noise levels in the whelping kennels. Regardless, the
hearing loss reported in these dachshunds that can be attributed to a genetic
cause is much lower than stated in the published English abstract of this German
publication.
In 2006 the gene
responsible for the merle pattern in dogs was identified and sequenced6
and a commercial DNA test is now available to determine whether a dog is a
single or double merle. In an unpublished study performed by myself and these
investigators at Texas A&M University,7 70 merle dogs from five
breeds (Shetland sheepdog, Australian shepherd, collie, Great Dane, and
Catahoula leopard dog) had BAER hearing tests performed and merle genotype
determined by DNA tests. Of 22 double merles, 8 were bilaterally deaf (36%) and
2 were unilaterally deaf (9%). Of 48 single merles only one was unilaterally
deaf (2%), a Great Dane that also carried the piebald gene, raising a questions
as to the cause for the deafness, and none was bilaterally deaf. Based on
Reetz’s study about one third of the single merles would have been expected to
have significant hearing loss.
An interesting
finding came from our group of 70 dogs: 15 of the double merles were Catahoulas,
but only 4 of them were deaf in one or both ears (27%), while 86% of the double
merles in the other breeds (Shetland sheepdog, Australian shepherd, collie) were
deaf. This suggests a breed difference for the impact of the merle gene on
hearing status, which may not be surprising since most double merle Catahoulas
are heavily pigmented compared to double merles in the other breeds. We are
continuing to test additional dogs to further document and understand these
differences.
What do
experienced breeders in merle-carrying breeds have to say? I cannot present any
numbers because I have not done formal surveys, but I’ve repeatedly heard from
long-time breeders who say that they seldom if ever get deaf or blind dogs from
breeding merle ✕
merle, especially in the dachshund and Catahoula breeds. There is no denying
that such outcomes do occur, especially, it would seem, in the collie-type
breeds, but we do not at this time know the determinants or conditions that
produce deaf or blind dogs.
What is to be
done, then, about the merle gene? It seems clear that merles in some breeds,
especially double merles, present a problem. In other breeds the problem is
significantly less problematic. It might be said that recent efforts in several
national breed clubs to ban merle completely from the breed standard is throwing
out the baby with the bath water. Others would argue that the production of even
small numbers of puppies with auditory or visual defects is an adequate reason
to eliminate the pattern. If we completely understood how merle works and what
determines deaf or blind merle puppies, it might be easier to assert with
confidence the right way to proceed. Leaving aside the ascetics of the merle
pattern appearance, a matter of personal preference, we can say with
confidence based on current data that single merles have a very low likelihood
of deafness. Double merles in some breeds – Catahoula, dachshund – have a finite
but still low probability of being deaf, while double merles in some other
breeds – the collie-type breeds – have a high likelihood of producing deaf.
Knowing how strongly double merle dogs are impacted within a breed should
provide guidance to breeders on whether they should avoid breeding double
merles. Researchers will provide some guidance, but unfortunately the studies
will take some time. In the mean time it seems prudent to delay making
difficult-to-reverse changes in breed standards based on limited information. In
most cases the breed standards have been in place for many decades; a few more
years of waiting won’t bring about the end of the world while we develop a
better understanding of merle.
References
1. Ostrander EA,
Wayne RK. 2005. The canine genome. Genetic Research 15: 706-1716.
2. Little CC. 1957.
The Inheritance of Coat Color in Dogs. New York: Howell Book House, 194
pp.
3. Strain GM. 2007.
Deafness in Dogs and Cats. http://www.lsu.edu/deafness.deaf.htm.
4. Reetz, I,
Stecker, M, & Wegner, W. 1977. Audiometrische Befunde in einer Merlezucht
[Audiometric findings in dachshonds (merle gene carriers)]. Deutsche
Tierärztliche Wochenschrift 84, 273-277.
5. Klinckmann G,
Koniszewski G, & Wegner W. 1986. Light-microscopic investigations on the retinae
of dogs carrying the merle factor. Journal of Veterinary Medicine A
33:674-688.
6. Clark LA, Wahl JM,
Rees CA, & Murphy KE. 2006. Retrotransposon insertion in SILV is responsible for
merle patterning of the domestic dog. Proceedings of the National Academy of
Sciences103:1376-81.
7. Clark, LA, Wahl
JM, Rees CA, Strain GM, Cargill EJ, Vanderlip SL, & Murphy KE. 2007. Canine
SINEs and their effects on phenotypes of the domestic dog. In: P. Gustafson, ed.
Genetics of Disease (in press).
The Author
George M. Strain is a
professor of neuroscience at the LSU School of Veterinary Medicine, where he has
studied deafness in dogs and cats for over twenty years. His training is in
electrical engineering, biomedical engineering, physiology, and neurology. More
information on deafness can be found on his Deafness in Dogs and Cats web site:
www.lsu.edu/deafness/deaf.htm.
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