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1.chromosome:
The
nuclear structure which houses (contains) the genetic information.
Chromosomes exist in pairs and therefore there are always two
copies of a given gene.
2.
gene:
a unit
of inheritance
3.
locus (-ci):
the
position of a gene on a chromosome. Every gene has a specific
locus
4.
genotype:
the
genetic make-up of an individual
5.
phenotype:
that part of the physical appearance of an organism which depends
on gene action
6.
homozygous:
the
condition when both alleles of a gene pair are identical
7.
heterozygous:
the
condition when both alleles of a gene pair are different
8.
dominant:
term
describing a gene which can produce a phenotype when present only
once; also the phenotype which results
9.
recessive:
term
describing a gene which must be present twice to produce a
phenotype; also refers to the phenotype which results
10.
wild:
the
"normal" phenotype
11.
mutant:
the
non-normal phenotype; is a relative term (relative to the
population from which the organism originates
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Color
Genes:
genes that affect the pigment color of hairs.
Pattern Genes:
genes that affect the distribution
of a particular color.
Different terms are sometimes used for the same genetic colors,
depending on breed and sometimes country too. In Border Collies, the
dilute brown, is called lilac. A dog that is genetically 'recessive red'
("e/e") is known as yellow in some breeds and red in others. Brown is
called chocolate by many and is also referred to as red. This can be
confusing.
MELANIN, AGOUTI AND RED:
Melanin is the substance that gives a
dog's hair its color. There are two distinct types of melanin in the
dog --- eumelanin and phaeomelanin.
Eumelanin
is, in
the absence of other modifying genes, black or dark brown.
Phaeomelanin
is, in its unmodified form, a yellowish color.
Melanin is produced by cells called melanocytes. These are found in the
skin, hair bulbs (from which the hairs grow) and other places. Melanocytes
within the hair follicles cause melanin to be added to the hair as it
grows. However, melanin is not added at a constant 'rate'. At the very
tip of the hair, eumelanin production is usually most intense, resulting
in the darker tip.
A protein called the Agouti protein has a major effect on the amount of
melanin injected into the growing hair. The Agouti protein causes a
banding effect on the hair: it causes a fairly sudden change from the
production of eumelanin (black/brown pigment) to phaeomelanin
(red/yellow pigment). An example of this coloration would be like the
color of a wild rabbit. The term 'Agouti' actually refers to a South
American rodent that exemplifies this type of hair.

The
Extension Locus - E
This refers to the extension of
eumelanin over the dog's body. The dominant form, "E", is normal
extension. The recessive form, "e", is non-extension. When a dog is
homozygous for non-extension (e/e), its coat will be entirely red/yellow
(phaeomelanin based). All dogs that have a brown (chocolate) coat will
have at least one "E" allele, because of the production of eumelanin.
The way to tell the difference between an Agouti red/yellow and an
Extension (e/e) red/yellow dog -- is the Agouti red/yellow almost always
have some black/brown hair in the coat (usually around the ears and
tail) and the Extension (e/e) dog won't. Another way is the Agouti
red/yellow must have at least one ("A^y") allele and can carry at most
one other agouti allele, the Extension (e/e) can carry any two Agouti
alleles (not necessarily "A^y").

DOMINANT
BLACK -- "K"
The dominant form of black:
completely dominates all formation of phaeomelanin pigment. In the past,
dominant black had been placed at the head of the Agouti series (symbol
"A^s"). Now, it has been proven to be part of a separate series, the "K"
series, and not at the Agouti locus at all.
Dominant black (K) is epistatic to whatever is found at the Agouti locus
(simply means that it causes the Agouti allele to act differently from
what it normally would), however; "e/e" is dominant to "K" at the E
locus.
When "K" is in the dominant form, "K/K" or "K/k", there would be no
expression from the A Locus and the color is dependant on what is at the
E Locus.
When "K" is in the homozygous recessive form "k/k", the coat color will
depend on what is located on the "E" and "A" Locus.
Dominant "K" codes for both dominant black and brindle in decreasing
order of dominance:
K -- dominant black (does not allow the A Locus alleles to be expressed)
br^k -- brindle (expressed when A Locus alleles are expressed)
k -- normal (allows the A Locus alleles to be expressed)
A dog
that is:
"K/K" or "K/k" -- dominant black;
dominant black carrying recessive black
"K^br" -- dominant black, carrying brindle
"br^br" -- brindled
"br^k" -- brindled, carrying recessive black
"k/k" -- 'normal' (recessive black)
Brindling
is 'stripes' of eumelanin-based (can be modified by the genes at the B
and D Locus, so the color could be black, blue, chocolate or lilac)
hairs in areas that are otherwise phaeomelanin based. In order to
produce the brindle color, at least one parent MUST be a brindle.
Brindle is dominant to its absence, so only one copy is needed. If a
person has a brindle colored pup for sale and there are no brindle
colors anywhere in the pedigree, then the sire that is reported on the
registration papers --- genetically can not be the (true) sire. There
is an exception to this if the dog is "e/e" or "K", he can be a carrier
of brindle.
It
is thought that the three loci E, K and A act together as follows:
If the dog is "e/e" at the E locus, and
at the K locus, it is "K", "br" or "k", its coat will be entirely
red/yellow (phaeomelanin based);
If the dog is E/E or E/e at the E locus, and at the K locus, it is "K",
its coat will be entirely dominant black (eumelanin based)
[**NOTE: the phenotypic color will depend on what is at the B, D, C and
M Locus];
If the dog is E/E or E/e at the E locus, and at the K locus, it is "br^br"
or "br^k" it will be brindled with the color of the phaeomelanin part of
the brindling affected by the Agouti alleles present;
If the dog is E/E or E/e at the E locus, and at the K locus, it is "k/k"
the distribution of eumelanin and phaeomelanin will be determined solely
by the Agouti alleles present.

The Agouti Locus - A
Simply, this is how the pigment is
distributed on the dog's body and hair shaft.
The Agouti locus controls the formation of the Agouti protein, that in
turn is one of the mechanisms that controls the replacement of eumelanin
with phaeomelanin in the growing hair. The alleles of the Agouti locus
can affect not just whether or not the eumelanin -- phaeomelanin shift
occurs, but also where on the dog's body this happens.
Two promoters are generally associated with the "wild type" version of
the agouti gene.
-
Cycling
Promoter
-
Ventral Promoter
The Cycling Promoter produces a banded
hair with a black tip and yellow middle over the entire body. If only
the action of this promoter is disrupted, the hair color on the dog's
back will be black and its belly and inside of the legs will be yellow.
This produces the black and tan color.
The Ventral Promoter dictates that there will be only yellow color in
the hair on the belly.The animal will have black banded hair on the
dorsal (back) side andpaler yellow hair on the ventral (belly) side. If
only the action of this promoter is disrupted, the hair color on the dog
will be banded over its entire body. This is said to be solid agouti
color.
If something inactivates the agouti protein, or if both promoters are
disrupted, the animal will appear to be solid black.
If a mutation occurs at one of these Promoters, this can cause the
yellow to be expressed over most of the body.
NOTE:
In part of a series on Dog Coat Color Genetics by Sheila Schmutz,
she
states that recent studies show that the
agouti signal peptide (ASIP) competes with melanocyte stimulating
hormone (MSH), which produces eumelanin pigments, to bind on the
melanocortin receptor and must sometimes win. Both the E allele and Em
allele are responsive to agouti or melanocortin binding in dogs. However
dogs that are ee have a mutation in MC1R and produce only phaeomelanin.
The dog's agouti genotype doesn't affect its coat color, which will be
some shade of cream, yellow or red.
To further complicate things, agouti has 2 separate and somewhat distant
promoters. Roughly, one seems to control ventral or belly color and the
other dorsal or back color. The simplest way to "see" this is on a black
and tan dog......the back is black from eumelanin pigment being made and
the belly is tan or red from phaeomelanin pigment being made.
The agouti gene has been mapped in the dog and DNA studies to determine
which patterns are under the control of this gene in the dog are in
progress. This gene undoubtedly has several alleles, but how many is
still an open question. Some have been identified using DNA studies and
tests for agouti phenotypes in some breeds may become available soon.
Although several books attempt to state thedominance hierarchy of the
agouti alleles, since no breed has all the alleles, it is not possible
to know this for sure. Most books suggest that it is aw > ay > at > a.
Breeding data and DNA data from our collaborative study with Dr. Greg
Barsh's group at Stanford supports this. However the data confirm
pairwise dominance/recessive
relationships in different families.......not the entire hierarchy in
one family.
Decreasing in order of dominance: (**sable may be dominant over wolf in
some breeders)
~~ "a^w", 'wolf' color
- This is
like "a^y" but the tan is replaced with a pale gray/cream color and the
hairs usually have several bands of light and dark color, not just the
black tip of sable. Example would be Keeshond, Siberian and Norwegian
Elkhound.
~~ "a^y", 'sable'
- also known as 'dominant yellow' or 'golden sable'. This results in an
essentially red/yellow phenotype, but the hair tips are black (eumelanin).
The extent of the eumelanin tip varies considerably from lighter sables
(where just the ear tips are black, called "Clear Sables") to darker
sables (where much of the body is dark, called "Shaded Sables").
~~ "a^s", 'saddle'
- Eumelanin is restricted to the back
and side regions, somewhat like the black/tan ("a^t") allele (below).
~~ "a^t", 'tan
points'
- This is primarily a solid
colored dog with tan (phaeomelanin) "points" above the eyes, muzzle,
chest, stomach and lower legs. The hue can range from a pale biscuit to
a rich ginger to a golden copper in color. In the Border Collie which
has the Irish spotting, along with tan points, this is known as "tri"
colored .
~~ "a"
- last of the Agouti series is recessive
black. When a dog is homozygous for recessive black (a/a), there will be
no red/yellow (phaeomelanin) in its coat (unless "e/e" is present, which
is epistatic to the Agouti series). Examples of breeds that show to be
recessive black are German Shepherd and Shetland Sheepdog.

BLACK
or
BROWN
(CHOCOLATE) - B GENE LOCUS: (pigment color)
This gene, when in the homozygous
recessive form, has a lightening effect on
eumelanin (black-based
colors) only. It has no effect on phaeomelanin (red-based colors).
It is believed that the Brown Locus codes for an enzyme, tyrosinase-related
protein 1 (TYRP1), which catalyzes the final step in eumelanin
production, changing the final intermediate brown pigment (dihydroxyindole)
to black pigment. SO, ALL dogs start as BROWN and after the final step
--- this directs the color to be black.
When brown (b/b) is expressed, it means that the final step in eumelanin
production has not been completed and the pigment remains brown. The
brown color is not a genetic defect.
When the alleles are in the homozygous or heterozygous dominant form of
B/B or B/b, the color and pigment (nose, eye rims and lips) remains (or
directs the color to be) black.
When the alleles are in the homozygous recessive form (b/b), the color
and pigment will be brown. This just means that the final step in
eumelanin production of changing brown to black did not occur.
Phaemelanin (yellow/red [e/e]) is not affected. BUT, in the e/e colored
dog, if the dog is also b/b; they'll be either red or yellow and will
have brown pigment (nose, eye rims and lips). The pigment
granules produced by "bb" are smaller, rounder in shape, and appear
lighter than pigment granules in "B" dogs. The iris of the eye is also
lightened.

DILUTION - D GENE LOCUS: (dilution of
pigment)
This gene
has an effect on both eumelanin and phaeomelanin.
When in the dominant form, "D/D" or "D/d", it allows for full color
(black or red).
When present in the homozygous recessive form (d/d) it dilutes black (eumelanin)
to blue, chocolate to lilac and red to cream.

COMBINATIONS OF B AND D IN EUMELANISTIC
COATS:
The effects of these 2 genes, when
combined, form a range of 4 eumelanistic ('black-based') colors:
The color of the pup/dog (Eumelanistic Color):
B/B D/D or B/b D/d will be black in color
B/B d/d or B/b d/d will be blue in color
b/b D/D or b/b D/d will be brown/chocolate
b/b d/d will be flat or dull diluted brown/chocolate

WHITE
SPOTTING - S GENE:
The "S" series alleles appear to be
incompletely dominant. In dogs it is thought there are four alleles that
deal with white spotting:
~~ "S"
- 'solid/self color'. Most dogs that are
homozygous for "S/S" have no white hair at all, or possible a tiny
amount, like a white tail tip.
~~ "s^i"
- 'irish spotting'. This involves white
spotting on most parts of the coat,
but not crossing the back beyond the
withers. This color pattern is evident on the Border Collie that have
the white collar.
New
research has proven that the white
undersides of the Border Collie is dictated by a different gene.
~~ "s^p"
- 'piebald'. The white is more extensive than irish spotting, and often
crosses the back. It is sometimes confused with the merle pattern. This
coloration usually has large colored spots on the body. The white covers
approximately 50% of the body.
~~ "s^w"
- 'extreme white piebald'. A dog that is homozygous for "s^w" will be
almost entirely white. This allelic pair is also responsible for the
"color headed" white dogs. Often times, along with a colored head, there
will also be a colored spot near the tail.

TICKED - T
GENE:
A dominant mutation that
causes the presence of color (flecks of color) in areas that have been
made white by the effect of alleles in the white spotting (S) series.
Ticked
("T/T") is incompletely dominant to non-ticked ("t/t").

ALBINO -
C GENE: (development of pigment)
The intensity of melanin production in
the coat hairs is affected by this gene. The dominant form, "C", is
termed 'full color'.
At this locus, almost all dogs are "C/C", or full color.
The lower series alleles, in order of decreasing dominance:
~~ "c^ch"
- Chinchilla -- It is an incomplete dominant gene. Chinchilla lightens
most or all of the red/yellow (phaeomelanin) with little or no effect on
black/brown (eumelanin). It turns black/tan to black/silver. In dogs,
this gene lightens yellow, tan or reddish phaeomelanin to cream. Since
there is little effect on the dark eumelanin, phaeomelanin is effected
more strongly than eumelanin and brown.
Dilute eumelanin (blue) is effected more strongly than dark (black)
eumelanin. When chinchilla is present, it dilutes brown to milk
chocolate, blue to silver and red to a butter cream color.
NOTE:
Newer
research indicates a chinchilla-like mutation occurs in dogs, although,
tyrosinase activity hasn't been shown to be connected. Therefore, some
other factor may be involved and the dog chinchilla allele may not
belong in this series. Also, there may be more than one form of the
chinchilla gene.
~~ "c^e" - is 'extreme dilution'. It causes tan to
become almost white. It is thought that the white labrador might be
"c^e" with another, lower, "C" series allele. The "c^e" allele may be
responsible for producing white hair, while allowing fullexpression of
dark nose and eye pigment. West Highland Terriers are thought to be e/e
c^e/c^e.
~~ "c^b"
- or blue-eyed albino. This
is an entirely white coat with a very small amount of residual pigment
in the eyes, giving pale blue eyes. It is also called platinum or
silver. This allelic pair could be responsible for the white coated,
pink skinned, blue-eyed Doberman's.
~~ "c^c"
- true pink-eyed albino. Has not been seen in dogs.

GRAYING - G GENE:
This is a dominant mutant gene that
causes the dog to gray with age. The pigmented hairs are progressively
replaced with unpigmented hairs.

MERLE - M
GENE:
The
only way a merle colored pup can be
produced is if at least one parent is merle. Some breeders are of the
understanding that the merle gene is a recessive gene and is carried
from generation to generation. This is not correct. The merle gene is
not carried, meaning -- the dog is either a merle or is not a merle.
There are no exceptions to this law of genetics (for now, at least,
until further research
is conducted).
If someone tells you that they have a litter of merled colored pups and
there are no merles for many generations in their bloodlines --- then
these merled pups were not sired by the sire the owner thinks there
were. In fact, he should look for the hole in the fence!
The merle gene is an incomplete dominant or a gene with intermediate
expression and is another dilution gene. Instead of diluting the whole
coat it causes a patchy dilution, with a black coat becoming gray
patched with black. Brown becomes dilute brown patched with chocolate,
sienna, brick, and various diluted brown colors. While sable merles can
be distinguished from sables, this is sometimes
very difficult because the merle coloration looks like -- to just
slightly different from -- the sable color. The merling is clearly
visible at birth, but may fade to little more than mottling of the ear
tips as an adult. Merling on the tan points of a merle black and tan is
not immediately obvious, either, though it does show if the mask factor
is present. Eyes of a merle dog are sometimes blue or marbled (brown
and blue segments in the eye).
A
"m/m"
(homozygous recessive)
dog is normal color (no merling). A
"M/m"
(heterozygous)
dog is a merle. A
"M/M" (homozygous dominant)
dog, known as a
double merle (from a merle to merle mating), has much
more white than is normal for the breed and may have hearing loss,
vision problems including small or missing eyes, and possible
infertility. The health effects seem worse if a gene for
white markings is also present. In Border Collies all of which normally
have
fairly extensive white markings, the "M/M" white has a strong
probability of being deaf or blind. A "M/M", double merle, to "mm",
non-merle black in color breeding, is the only one that will produce
100% merles.
Cryptic or phantom (as it's sometimes called) merles are dogs which
carry a merle gene but are phenotypically (look like) tri, bi or self
colored. These dogs will have some small area of merling somewhere,
usually a tiny patch of merle pattern on their ear, tail, top of head,
etc. Keep in mind the tiny patch can be only one hair and it can be
located anywhere on the body. Cryptic merles are very rare. AGAIN, a
cryptic or visible merle can only be produced when one or both parents
are merles.

GENOTYPES AND
COLORS:
("-" is either the dominant or recessive allele)
B/- D/- E/- K/- = black
b/b D/- E/- K/- = brown (chocolate)
B/- d/d E/- K/- = blue
b/b d/d E/- K/- = lilac
AGOUTI:
at^at B/- D/- E/- k/k = black with tan
points
at^at b/b D/- E/- k/k = chocolate with tan points
at^at B/- d/d E/- k/k = blue with dilute tan points
at^at b/b d/d E/- k/k = lilac with dilute tan points
NON-EXTENSION RED (cream):
B/B d/d e/e
= dilute red to pale cream with gray nose (dog is genetically a dilute
black, but will be a cream color)
B/b d/d e/e
= dilute red to pale cream with gray nose (dog is genetically a dilute
black, but will be a cream color)
b/b d/d e/e
= dilute red to pale cream with rosey-brown nose (dog is genetically
dilute brown, but will be cream color)
b/b D/d e/e
= dilute red to pale cream with brown nose (dog is genetically brown,
but will be cream color)
b/b D/D e/e
= dilute red to pale cream with brown nose (dog is genetically brown,
but will be cream color)
B/B D/D e/e
= dilute red to pale cream with black nose (dog is genetically black,
but will be cream color)
B/b D/d e/e
= dilute red to pale cream with black nose (dog is genetically black,
but will be cream color)

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