Cat coat genetics

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This cat's coat allows it to blend in well with its environment
This cat's coat allows it to blend in well with its environment

The genetics of cat coat coloration, pattern, length, and texture is a complex subject, and many different genes are involved.

Contents

[edit] Genes involved in albinism, dominant white, and white spotting

The temperature sensitive albino genotype cscs produces point coloration at body extremities where lower temperature allows the mutated Tyrosinase enzyme to become active.
The temperature sensitive albino genotype cscs produces point coloration at body extremities where lower temperature allows the mutated Tyrosinase enzyme to become active.
  • The dominant C gene codes for the enzyme tyrosinase, the first step in pigment production. Its recessive alleles determine whether a cat is a complete albino (pink-eyed) or a temperature sensitive albino. The temperature sensitive albino genotypes are cbcb Burmese (sepia), cscs Siamese (pointed), and cbcs Tonkinese (mink). If a cat has the dominant C allele, then the cat is non-albino and full pigment production occurs.
  • The white masking gene, W/w. The dominant allele of this gene masks all other colors by preventing normal pigment producing cell replication and migration to the skin during embryologic development. These cats have a greatly reduced number of melanocytes. Although often called a "dominant" gene it would more correctly be called epistatic, as it masks the effects of all other color genes. A cat that is WW or Ww will be white, no matter what other color genes it may have. A cat that is homozygous recessive (ww) will express normal pigmentation. Some cats with the W allele of this gene are deaf and/or have depigmentation of the iris of one or both eyes, resulting in blue eye color. White cats are also more likely to get skin cancer.
  • The white spotting or piebald spotting gene, S/s, has variable expression, so that an SS cat often has more extensive white patching than an Ss cat. It is this gene that creates the familiar white blaze across the face, a white bib, tuxedo pattern, or dappled paws. This gene can turn a cat's eyes blue due to a reduced number of melanocytes, affecting pigmentation of the eyes. A hypothetical Sb allele ("gloving gene") may cause the mittens in Birman and Snowshoe breeds. Some researchers believe that there are separate white spotting genes for distinct forms of white pattern, such as the white locket that some cats have on their neck or bellies.

[edit] Genes involved in orange, black, brown, and diluted colors

  • The sex-linked orange gene, O, determines if there will be orange fur. This gene is located on the X chromosome. In cats with orange fur, phaeomelanin (orange pigment) completely replaces eumelanin (black or brown pigment).
  • Males have only one X chromosome, so only have one allele of this gene. O results in orange fur, and o results in non-orange fur.
  • Since females have two X chromosomes, they have two alleles of this gene. OO results in orange fur, oo results in non-orange fur, and Oo results in a tortoiseshell cat, in which some parts of the fur are orange and others areas non-orange. A cat with Oo and white spotting genes is commonly called a calico. The reason for the patchwork effect in female cats heterozygous for the O gene (Oo) is X-inactivation - one or the other X chromosome in every cell in the embryo is randomly inactivated (see Barr body), and the gene in the other X chromosome is expressed.
  • Rufous polygenes, as yet unidentified, can affect the richness of the orange gene's expression.

For a cat to be tortoiseshell, calico, or one of the variants such as blue-cream or chocolate tortoiseshell, the cat must simultaneously express two alleles, O and o, which are located on the X chromosome. Males normally cannot do this, as they have only one X chromosome, and therefore only one allele, and so calico cats are normally only female. Male tortoiseshell or calico cats occur only if they have chromosomal abnormalities such as the genotype XXY (in which case they are sterile), chromosomal mosaicism (only portions of their cells have the genotype XXY, so these cats may be fertile), or chimericism (a single individual formed from two fused embryos, at least one of which was male). Approximately 1 in 1000 calico/tortoiseshell cats are male. Chimericism (which may result in fertile male cats) appears to be the most common mechanism.

  • The browning gene B/b/bl codes for tyrosinase related protein-1, an enzyme involved in the metabolic pathway for eumelanin pigment production. Its dominant form, B, will produce black color. Recessive variants are b, producing brown (or chocolate), and bl producing light brown or cinnamon.
  • Barrington Brown is a recessive browning gene that dilutes black to mahogany, brown to light brown and chocolate to pale coffee. It is different from the browning gene and has only been observed in laboratory cats.
  • The Dense pigment gene, D/d, codes for melanophilin, a protein involved in the transportation and deposition of pigment into a growing hair. When a cat has two of the recessive d alleles (Maltese dilution), black fur becomes "blue" (appearing gray), chocolate fur becomes "lilac" (appearing light brown), cinnamon fur becomes fawn, and orange fur becomes cream.
  • Dilution modifier gene, Dm, "caramelizes" the dilute colors as a dominant trait. The existence of this phenomenon as a discrete gene is a controversial subject among feline enthusiasts.
  • There is also a theoretical "black modifier" gene, Bm, which in its recessive form, bmbm, causes tabby cats to turn into the colors amber or light amber. This gene could be more appropriately called "agouti modifier" and is probably related to the extension locus (the melanocortin receptor) or its ligands, melanocyte stimulating hormone and agouti signaling protein. This phenomenon was first identified in Norwegian Forest Cats. Other forms of extension mutations have been seen in many breeds (and domestic cats), resulting in unique forms of tabby expression.
  • A modifying factor has also been hypothesized in shaded silver and chinchilla Persians whose fur turns pale golden in adulthood, due to low levels of phaeomelanin production. These cats resemble shaded or tipped goldens, but are genetically shaded or tipped silvers. This is probably related to the phenomenon known as "tarnishing" in silvers.

One can deduce that a grey male cat with a white bib and paws:

  • has the o variant of the orange gene on its only X chromosome (because the grey color corresponds to black, not orange)
  • has at least one S variant of the white Spotting gene (because it has the white bib and paws)
  • has two w alleles (because it expresses a fur color)
  • has the dominant B allele (because its fur color is a shade of black rather than brown)
  • has two d (dilute) alleles (because its fur is grey, rather than black)

[edit] Genes involved in fur pattern and shading

  • The agouti gene, A/a which codes for agouti signaling protein. The dominant, wild-type A causes the agouti shift phenomenon which causes hairs to be black pigmented at the tips and orange pigmented at the roots (revealing the underlying tabby pattern), while the recessive non-agouti or "hypermelanistic" allele, a, prevents this shift in the pigmentation pathway. In its homozygous form, aa, this results in black pigment production throughout the growth cycle of the hair. Thus, the non-agouti genotype (aa) masks or hides the tabby pattern, although sometimes a suggestion of the underlying pattern can be seen (called "ghost striping"), especially in kittens. The O allele is also epistatic over the aa genotype. That is, the A to a mutation does not have a discernible effect on red or cream colored cats, resulting in these cats displaying tabby striping independent of their genotype at this locus. This explains why you can usually see the tabby pattern in the orange patches of non-agouti tortoiseshell cats, but not in the black or brown patches.
Mackerel tabby with the classic "M" on forehead.
Mackerel tabby with the classic "M" on forehead.
The recessive mutant gene mc produces the blotched or classic tabby pattern.
The recessive mutant gene mc produces the blotched or classic tabby pattern.
White cat with black spotting.
White cat with black spotting.
  • The primary tabby pattern gene, Mc/mc, sets the basic pattern of stripes that underlies the coat: the basic wild-type tabby gene, Mc, produces what is called a mackerel striped tabby (stripes look like thin fishbones and may break up into bars or spots); while a recessive mutant, mc, produces a blotched or classic tabby pattern (broad bands, whorls, and spirals of dark color on pale background usually with bulls-eye or oyster pattern on flank), common to Great Britain and in lands that were once part of the British Empire.
  • Secondary tabby pattern genes such as Ta / ta, at which locus a dominant mutation produces an Abyssinian ticked or non-patterned agouti tabby, having virtually no stripes or bars. (This is one type of unpatterned tabby; the other type of unpatterned tabby is the shaded/chinchilla. See inhibited pigment gene, below.) The dominant ticked tabby allele masks all other tabby patterns.
  • Other genes (pattern modifier genes) are theorized to be responsible for creating various type of spotting patterns, many of which are variations on a basic mackerel or classic pattern. There are also hypothetical factors which affect the timing and frequency of the agouti shift, affecting agouti band width and the number and quality of alternating bands of eumelanin and phaeomelanin on individual hairs.
Brown Mackerel tabby cat with pencil lines on the face.
Brown Mackerel tabby cat with pencil lines on the face.

Tabby cats (AA or Aa), normally have:

  • M on forehead. (Visible in ticked tabby cats, but hard to discern in shaded silver/golden, and tipped cats)
  • Thin pencil lines on face. (Visible in ticked tabby cats, but hard to discern in shaded silver/golden, and tipped cats)
  • Black "eyeliner" appearance and white or pale fur around eyeliner.
  • Pigmented lips and paws.
  • A pink nose outlined in darker pigment
  • Torso, leg, and tail banding. (Torso banding disappears in the ticked tabby.)

Most or all striping disappears in the chinchilla or shaded cat, but you can still identify the cat as a tabby from these other features.

  • There is an interesting gene, not yet identified but believed to be related to the agouti gene, in the Chausie breed, that produces silver-tipped black fur similar to Abyssinian ticked fur. The "grizzled" phenomenon is purported to have been inherited from the hybridization of domestic cats to Jungle Cats.
  • The inhibited pigment gene, I/i. The dominant allele (I) produces tipped hairs that are fully colored only at the tip and have a white base. This allele appears to interact with other genes to produce various degrees of tipping, ranging from deeply tipped silver tabby to lightly tipped shaded silver and chinchilla silver. The inhibitor gene interacts with the non-agouti genotype (I-aa) to produce the color known as smoke. The homozygous recessive genotype when combined with the agouti gene (iiA-), produces tabby coloration, which can vary along a spectrum ranging from a deeply patterned brown tabby, to a lighter "golden tabby", to the very lightly colored shaded or chinchilla golden colors. Orange cats with the inhibitor gene (I-O-) are commonly called "cameo".

The genetics involved in producing the ideal tabby, tipped, shaded, or smoke cat is complex. Not only are there many interacting genes, but genes sometimes do not express themselves fully, or conflict with one another. For example, the melanin inhibitor gene sometimes does a poor job blocking pigment, resulting in an excessively gray undercoat, or in tarnishing (yellowish or rusty fur). Likewise, poorly-expressed non-agouti or over-expression of melanin inhibitor will cause a pale, washed out black smoke. Various polygenes (sets of related genes), epigenetic factors, or modifier genes, as yet unidentified, are believed to result in different phenotypes of coloration, some deemed more desirable than others by fanciers.

Here are the genetic influences on tipped or shaded cats:

  • Agouti gene.
  • Tabby pattern genes (such as Ta masking the tabby pattern).
  • Silver or melanin inhibitor gene.
  • Factors affecting the number and width of bands of color on each hair (such as the hypothetical wide band gene).
  • Factors affecting the amount and quality of eumelanin and/or phaeomelanin pigment expression (such as theorized rufousing factors)
  • Genes causing sparkling appearance (such as glitter in the Bengal, satin in the Tennessee Rex, grizzle in the Chausie).
  • Factors to clear up residual striping (hypothetical Chaos, Confusion, Unconfused, Erase, and Roan factors).

[edit] Genes involved in fur length and texture

Cat fur length is governed by the Long hair gene in which the dominant form, L codes for short hair, and the recessive l codes for long hair. In the longhaired cat, the transition from anagen (hair growth) to catagen (cessation of hair growth) is delayed due to this mutation. A rare recessive shorthair gene has been observed in some lines of Persian cat (silvers) where two longhaired parents have produced shorthaired offspring.

There have been many genes identified that result in unusual cat fur. These genes were discovered in random-bred cats and selected for. Some of the genes are in danger of going extinct because the cats are not sold beyond the region where the mutation originated or there is simply not enough demand for cats expressing the mutation.

In many breeds, coat mutation genes are unwelcome. An example is the rex allele which appeared in Maine Coons in the early 1990's. Rexes appeared in America, Germany and the UK, where one breeder caused consternation by calling them "Maine Waves". Two UK breeders did test mating which indicated that this was probably a new rex mutation and that it was recessive. The density of the hair was similar to normally coated Maine Coons, but consisted only of down type hairs with a normal down type helical curl, which varied as in normal down hairs. Whiskers were more curved, but not curly. Maine Coons do not have awn hairs, and after moulting, the rexes had a very thin coat.

There are various genes producing curly coated or "rex" cats. New types of rex pop up spontaneously in random-bred cats now and then. Here are some of the rex genes that breeders have selected for:

  • r = Cornish Rex, recessive.
  • gr (provisional) = German Rex, recessive. Same locus as Cornish, but proposed as a different allele. However, most breeders consider the German Rex to have r/r genotype.
  • re = Devon Rex, recessive.
  • ro = Oregon Rex (extinct), recessive.
  • Se = Selkirk Rex, dominant although sometimes described as an incomplete dominant because the three possible allele parings relate to three different phenotypes: heterozygous cats (Sese) may have a fuller coat that is preferred in the show ring, while homozygous cats (SeSe) may have a tighter curl and less coat volume. (sese type cats have a normal coat.) This phenomenon may also coloquially be referred to as additive dominance.
  • Lp (provisional) = LaPerm, dominant: Lp/lp and Lp/Lp individuals have the same phenotype.

There are also genes for hairlessness:

Some rex cats are prone to temporary hairlessness, known as baldness, during moulting.

Here are a few other genes resulting in unusual fur:

  • The Wh gene (dominant, possibly incomplete) results in Wirehair cats. They have bent or crooked hair producing springy, crinkled fur.
  • A hypothetical Yuc gene, or York Chocolate undercoat gene, results in cats with no undercoat. However, the proportional relationship between guard, awn, and down hair production varies greatly between all breeds.
  • A recessive autosomal gene for Onion hair which causes roughness and swelling on the hairs. The swelling is due to enlargement of the inner core of medulla cells.
  • A recessive autosomal gene spf for sparse fur. As well as sparse coat, the hairs are thin, straggly and contorted and there is brown exudate around the eyes and nose and on the chest and stomach. A similar condition is linked to Ornithine Transcarbamylase Deficiency in mice.

[edit] See also

[edit] References

[edit] External links

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