White horse | |
---|---|
Genotype | |
Base color | Dominant white |
Skin | White |
A white horse is born predominantly white and stays white throughout its life. A white horse has mostly pink skin under its hair coat, and may have brown, blue, or hazel eyes. "True white" horses, especially those that carry one of the dominant white (W) genes, are rare. Most horses that are commonly referred to as "white" are actually "gray" horses whose hair coats are completely white. Gray horses may be born of any color and their hairs gradually turn white as time goes by and take on a white appearance. Nearly all gray horses have dark skin, except under any white markings present at birth. Skin color is the most common method for an observer to distinguish between mature white and gray horses. [1]
White horses have unpigmented skin and a white hair coat. Many white horses have dark eyes, though some have blue eyes. In contrast to gray horses which are born with pigmented skin they keep for life and pigmented hair that lightens to white with age, truly white horses are born with white hair and mostly pink, unpigmented skin. Some white horses are born with partial pigmentation in their skin and hair, which may or may not be retained as they mature, but when a white horse lightens, both skin and hair lose pigmentation. In contrast, grays retain skin pigment and only the hair becomes white.
White colorings, whether white markings, white patterns or dominant white are collectively known as depigmentation phenotypes, and are all caused by areas of skin that lack pigment cells (melanocytes). [2] Depigmentation phenotypes have various genetic causes, and those that have been studied usually map to the EDNRB and KIT genes. However, much about the genetics behind various all-white depigmentation phenotypes are still unknown.
Dominant white (W) is a large group of alleles best known for producing pink-skinned all-white horses with brown eyes, though some dominant white horses have residual pigment along the topline. Some W alleles produce white spotting on horses with a predominately dark coat. Dominant white has been studied in Thoroughbreds, Arabian horses, the American White horse, the Camarillo White Horse, and several other breeds. There are 32 identified variants of dominant white as of 2021, plus sabino 1, each corresponding to a spontaneously-white foundation animal and a mutation on the KIT gene. Researchers have suggested that at least some forms of dominant white result in nonviable embryos in the homozygous state, though others are known to be viable as homozygotes. While homologous mutations in mice are often linked to anemia and sterility, no such effects have been observed in dominant white horses. Dominant white horses typically have white noses that can be subject to sunburn.
Sabino-white horses are pink-skinned with all-white or nearly-white coats and dark eyes. They are homozygous for the dominant SB1 allele at the Sabino 1 locus, which has been mapped to KIT . [5] Sabino-white was one of the earliest dominant white alleles discovered, but was not originally recognized as such, hence the different name. The Sabino1 allele, and the associated spotting pattern, is found in Miniature horses, American Quarter Horses, American Paint Horses, Tennessee Walkers, Missouri Fox Trotters, Mustangs, Shetland Ponies, and Aztecas. [6] Sabino 1 has not been found in the Arabian horse, Clydesdale, [5] Thoroughbred, Standardbred horse, or Shire horse. The Sabino 1 allele is not linked to any health defects, though sabino-whites may need some protection from sunburn. Horses with only one copy of the Sabino1 gene usually have dramatic spotting, including two or more white legs, often with white running up the front of the leg, extensive white on the face, spotting on the midsection, and jagged or roaned margins to the pattern. [5]
The leopard complex, related to the Leopard (LP) gene, characterizes the Appaloosa and Knabstrupper breeds with their spotted coats. Leopard is genetically quite distinct from all other white and white-spotting patterns. The fewspot leopard pattern, however, can resemble white. Two factors influence the eventual appearance of a leopard complex coat: whether one copy (heterozygous LP/lp) or two copies (homozygous LP/LP) Leopard alleles are present, and the degree of dense white patterning present at birth. [7] If a foal is homozygous for the LP allele and has extensive dense white patterning, they will appear nearly white at birth, and may continue to lighten with age. In other parts of the world, these horses are called "white born." [8] "White born" foals are less common among Appaloosa horses than Knabstruppers or Norikers, as the extensive dense white patterning is favored for producing dramatic full leopards. Homozygous leopards have the LP/LP genotype, and may be varnish roan, fewspot leopard, or snowcap patterned. Homozygous leopards are substantially more prone to congenital stationary night blindness. [9] Congenital stationary night blindness is present at birth and is characterized by impaired vision in dark conditions.
Lethal white syndrome is a genetic disorder linked to the Frame overo (O) gene and most closely studied in the American Paint Horse. Affected foals are carried to term and at birth appear normal, though they have pink-skinned all-white or nearly-white coats and blue eyes. However, the colon of these foals cannot function due to the absence of nerve cells, and the condition cannot be treated. Foals with Lethal White Syndrome invariably die of colic within 72 hours, and are usually humanely euthanized. Carriers of the gene, who are healthy and normal, can be identified by a DNA test. While carriers often exhibit the "frame overo" pattern, this is not a dispositive trait and testing is necessary, as the pattern can appear in a minimal form as normal white markings or be masked by other white spotting genes.
Genetically white horses have unpigmented pink skin (except where a horse with a W allele may have some darker pigmented areas) and unpigmented white hair, though eye color varies. The lack of pigment in the skin and hair is caused by the absence of pigment-producing cells called melanocytes. Some coat colors are characterized by light or white-like coats and even pinkish skin, however these white-like coats are not lacking melanocytes. Instead, white-like coat colors result from various changes in the ways melanocytes produce pigment.
Gray horses have the most common "white-like" coat color. However, the most noticeable difference between a gray horse whose hair coat is completely white and a white horse is skin color: most gray horses have black skin and dark eyes, white horses have light, unpigmented skin. The gray gene does not affect skin or eye color, so grays typically have dark skin and eyes, as opposed to the unpigmented pink skin of true white horses. [10] The skin and eyes may be other colors if influenced by other factors such as white markings, certain white spotting patterns or dilution genes. Gray foals may be born any color, but the colored hairs of their coat become progressively silvered as they age, eventually giving mature gray horses a white or nearly-white hair coat. Gray is controlled by a single dominant allele of a gene that regulates specific kinds of stem cells. [11] Gray horses are at an increased risk for melanoma; 70-80% of gray horses over the age of 15 have a melanoma tumor. [11]
True white hair is rooted in unpigmented skin that lacks melanocytes. In contrast, diluted coat colors have melanocytes, but vary due to the concentration or chemical structure of the pigments made by these pigment-producing cells, not the absence of the cells themselves. There are at least five known types of pigment dilution in horses, three which, as described below, can act to produce off-white phenotypes. Horses with strongly diluted coat colors usually have pale eyes (usually blue), cream-colored coats, and rosy-pink skin that contains a minimal amount of pigment. White markings are usually visible upon closer inspection.
Although white horses are sometimes called "albino" there are few cases of a true "albino" horse. [15] There are also references in literature calling white horses "albino". [16] Dominant white in horses is caused by the absence of pigment cells (melanocytes), whereas albino animals have a normal distribution of melanocytes. [17] In other animals, patches of unpigmented skin, hair, or eyes due to the lack of pigment cells (melanocytes) are called piebaldism, not albinism nor partial albinism.
All so-called "albino" horses have pigmented eyes, generally brown or blue. While true albino horses will have a pale blue or white eye. In contrast, many albino mammals, such as mice or rabbits, typically have a white hair coat, unpigmented skin and reddish eyes. The definition of "albinism" varies depending on whether humans, other mammals, or other vertebrates are being discussed. [18]
Despite this, some registries still refer to "albino" horses. For example, the Paso Fino Horse Association registers cremellos and other cream colors as "albino." [19] Until 1999, the American Quarter Horse Association (AQHA) described perlino or cremello horses as "albino" in rule 227(j). [20] The AQHA later replaced the word "albino" with "cremello or perlino," and in 2002 the rule was removed entirely. Among Connemara pony breeders, homozygous creams are called "blue-eyed creams" or sometimes "pseudo-albino". [21]
The best-known type of albinism is OCA1A, which impairs tyrosinase production. In other mammals, the diagnosis of albinism is based on the impairment of tyrosinase production through defects in the Color (C) gene. [22] Mice and other mammals without tyrosinase have unpigmented pink skin, unpigmented white hair, unpigmented reddish eyes, and some form of vision impairment. No mutations of the tyrosinase or C gene are known in horses. [15]
Humans exhibit a wide range of pigmentation levels as a species. However, the diagnosis of albinism in humans is based on visual impairment, which has not been described in white horses. [23] Vision problems are not associated with gray, dilute, or white coat colors in horses, and blue eyes in horses do not indicate poor vision. Eyes are pigmented at the front of the iris called the stroma, and in a thin layer at the back of the iris in tissue called the iris pigment epithelium. The iris pigment epithelium prevents damaging light scattering within the eye. Blue-eyed humans and mammals have little or no pigment in the stroma, but retain pigment in the iris pigment epithelium. If pigment is missing from both the stroma and the iris pigment epithelium, the only pigment in the eye is the hemoglobin in blood vessels. This accounts for the reddish appearance of eyes in some types of albinism. [24]
In research mammals, such as mice, albinism is more strictly defined. Albino mice occur due to a recessive mutation of the C gene. No such mutation exists in horses. [15] Albino mice lack pigment, but "...the inability of albino animals to produce pigment stems not from an absence of melanocytes...but from a deficiency and/or alteration of the structure of tyrosinase in melanocytes which are otherwise normal." [17] This definition of albinism in mice – the inability to make tyrosinase – is extended to other mammals. [22]
While mammals derive their pigments only from melanins, fish, reptiles and birds rely on a number of pigments apart from melanins: carotenoids, porphyrins, psittacofulvins, pterins, etc. [18] [25] Most commonly, reptiles with a condition homologous to human OCA1A retain their reddish and orangish hues. As a result, birds and reptiles without the ability to manufacture tyrosinase are more accurately described as "amelanistic." Horses do not have non-melanin pigments and so if they were albino, would have no pigmentation. The retained pigment of dilute horses, like cremellos, is not comparable to the retained pigment of amelanistic "albino" birds and reptiles.
The cream gene, which is responsible for palomino, buckskin, and cremello coat colors, was mapped to the MATP gene in 2003 (now known as SLC45A2). [26] This gene is sometimes called the OCA4 gene, because one mutation on SLC45A2 is associated with Oculocutaneous albinism type 4. However, other mutations in SLC45A2 are responsible for normal variations in skin, hair, and eye color in humans and . [27] Although SLC45A2 is not the "albino gene"; one of many mutations of the human SLC45A2 is responsible for a form of albinism. [28]
Many famous horses, past and present, were alleged to be "white" by observers, but were actually grays with hair coats turned fully white. Likewise, most white horses used in movies are actually grays, in part because they are easier to find. However, there are a few truly white horses who were used in film. One of the best-known examples was "Silver," ridden by the Lone Ranger, a role actually played by two different white horses. At least one horse who played "Topper," ridden by Hopalong Cassidy, was also white.
Another famous white horse is Sodashi, a Japanese Thoroughbred racehorse who won Grade 1 races including Hanshin Juvenile Fillies, Oka Sho (Japanese 1,000 Guineas), and Victoria Mile. [29] [30]
Throughout history, white horses have been mythologized in many cultures. For example, Herodotus reported that white horses were held as sacred animals in the Achaemenid court of Xerxes the Great (ruled 486–465 BC), [31] In more than one tradition, a white horse carries patron saints or the world saviour in the end times, including Hinduism, Christianity, and Islam. [ citation needed ]
A dilution gene is any one of a number of genes that act to create a lighter coat color in living creatures. There are many examples of such genes:
Cat coat genetics determine the coloration, pattern, length, and texture of feline fur. The variations among cat coats are physical properties and should not be confused with cat breeds. A cat may display the coat of a certain breed without actually being that breed. For example, a Neva Masquerade could wear point coloration, the stereotypical coat of a Siamese.
Lethal white syndrome (LWS), also called overo lethal white syndrome (OLWS), lethal white overo (LWO), and overo lethal white foal syndrome (OLWFS), is an autosomal genetic disorder most prevalent in the American Paint Horse. Affected foals are born after the full 11-month gestation and externally appear normal, though they have all-white or nearly all-white coats and blue eyes. However, internally, these foals have a nonfunctioning colon. Within a few hours, signs of colic appear; affected foals die within a few days. Because the death is often painful, such foals are often humanely euthanized once identified. The disease is particularly devastating because foals are born seemingly healthy after being carried to full term.
A piebald or pied animal is one that has a pattern of unpigmented spots (white) on a pigmented background of hair, feathers or scales. Thus a piebald black and white dog is a black dog with white spots. The animal's skin under the white background is not pigmented.
Bay is a hair coat color of horses, characterized by a reddish-brown or brown body color with a black point coloration on the mane, tail, ear edges, and lower legs. Bay is one of the most common coat colors in many horse breeds.
A gray horse has a coat color characterized by progressive depigmentation of the colored hairs of the coat. Most gray horses have black skin and dark eyes; unlike some equine dilution genes and some other genes that lead to depigmentation, gray does not affect skin or eye color. Gray horses may be born any base color, depending on other color genes present. White hairs begin to appear at or shortly after birth and become progressively more prevalent as the horse ages as white hairs become intermingled with hairs of other colors. Graying can occur at different rates—very quickly on one horse and very slowly on another. As adults, most gray horses eventually become completely white, though some retain intermixed light and dark hairs.
The cream gene is responsible for a number of horse coat colors. Horses that have the cream gene in addition to a base coat color that is chestnut will become palomino if they are heterozygous, having one copy of the cream gene, or cremello, if they are homozygous. Similarly, horses with a bay base coat and the cream gene will be buckskin or perlino. A black base coat with the cream gene becomes the not-always-recognized smoky black or a smoky cream. Cream horses, even those with blue eyes, are not white horses. Dilution coloring is also not related to any of the white spotting patterns.
The champagne gene is a simple dominant allele responsible for a number of rare horse coat colors. The most distinctive traits of horses with the champagne gene are the hazel eyes and pinkish, freckled skin, which are bright blue and bright pink at birth, respectively. The coat color is also affected: any hairs that would have been red are gold, and any hairs that would have been black are chocolate brown. If a horse inherits the champagne gene from either or both parents, a coat that would otherwise be chestnut is instead gold champagne, with bay corresponding to amber champagne, seal brown to sable champagne, and black to classic champagne. A horse must have at least one champagne parent to inherit the champagne gene, for which there is now a DNA test.
Equine coat color genetics determine a horse's coat color. Many colors are possible, but all variations are produced by changes in only a few genes. Bay is the most common color of horse, followed by black and chestnut. A change at the agouti locus is capable of turning bay to black, while a mutation at the extension locus can turn bay or black to chestnut.
The dun gene is a dilution gene that affects both red and black pigments in the coat color of a horse. The dun gene lightens most of the body while leaving the mane, tail, legs, and primitive markings the shade of the undiluted base coat color. A dun horse always has a dark dorsal stripe down the middle of its back, usually has a darker face and legs, and may have transverse striping across the shoulders or horizontal striping on the back of the forelegs. Body color depends on the underlying coat color genetics. A classic "bay dun" is a gray-gold or tan, characterized by a body color ranging from sandy yellow to reddish brown. Duns with a chestnut base may appear a light tan shade, and those with black base coloration are a smoky gray. Manes, tails, primitive markings, and other dark areas are usually the shade of the undiluted base coat color. The dun gene may interact with all other coat color alleles.
Chestnut is a hair coat color of horses consisting of a reddish-to-brown coat with a mane and tail the same or lighter in color than the coat. Chestnut is characterized by the absolute absence of true black hairs. It is one of the most common horse coat colors, seen in almost every breed of horse.
Horses exhibit a diverse array of coat colors and distinctive markings. A specialized vocabulary has evolved to describe them.
Black is a hair coat color of horses in which the entire hair coat is black. It is not uncommon to mistake dark chestnuts or bays for black.
Sabino describes a distinct pattern of white spotting in horses. In general, Sabino patterning is visually recognized by roaning or irregular edges of white markings, belly spots, white extending past the eyes or onto the chin, white above the knees or hocks, and "splash" or "lacy" marks anywhere on the body. Some sabinos have patches of roan patterning on part of the body, especially the barrel and flanks. Some sabinos may have a dark leg or two, but many have four white legs. Sabino patterns may range from slightly bold face or leg white markings—as little as white on the chin or lower lip—to horses that are fully white.
The genetic basis of coat colour in the Labrador Retriever has been found to depend on several distinct genes. The interplay among these genes is used as an example of epistasis.
The leopard complex is a group of genetically related coat patterns in horses. These patterns range from progressive increases in interspersed white hair similar to graying or roan to distinctive, Dalmatian-like leopard spots on a white coat. Secondary characteristics associated with the leopard complex include a white sclera around the eye, striped hooves and mottled skin. The leopard complex gene is also linked to abnormalities in the eyes and vision. These patterns are most closely identified with the Appaloosa and Knabstrupper breeds, though its presence in breeds from Asia to western Europe has indicated that it is due to a very ancient mutation.
Amelanism is a pigmentation abnormality characterized by the lack of pigments called melanins, commonly associated with a genetic loss of tyrosinase function. Amelanism can affect fish, amphibians, reptiles, birds, and mammals including humans. The appearance of an amelanistic animal depends on the remaining non-melanin pigments. The opposite of amelanism is melanism, a higher percentage of melanin.
Dominant white (W) is a group of genetically related coat color alleles on the KIT gene of the horse, best known for producing an all-white coat, but also able to produce various forms of white spotting, as well as bold white markings. Prior to the discovery of the W allelic series, many of these patterns were described by the term sabino, which is still used by some breed registries.
In poultry standards, solid white is coloration of plumage in chickens characterized by a uniform pure white color across all feathers, which is not generally associated with depigmentation in any other part of the body.
Albinism is the congenital absence of melanin in an animal or plant resulting in white hair, feathers, scales and skin and reddish pink or blue eyes. Individuals with the condition are referred to as albinos.
Phenotypes may vary from tiny depigmentated body spots to white head and leg markings, further on to large white spotting and finally nearly complete depigmentation in white-born horses...White markings result from the lack of melanocytes in the hair follicles and the skin...A completely pigmented head or leg depends on the complete migration and clonal proliferation of the melanoblasts in the mesoderm of the developing fetus, thus ensuring that limbs and the head acquire a full complement of melanocytes
Horses with 2 copies of the Sabino1 gene, are at least 90% white and are referred to as Sabino-white.
The progressive loss of colour in the hair of gray horses is controlled by a dominantly inherited allele at the Gray locus (GG). Foals are born any colour depending on the alleles present at other colour determining loci. After birth, horses carrying the GG allele begin to show white hairs that are intermixed with their original hair colour. Although the rate at which horses will turn gray is variable, the amount of white hair increases with age until the coat is completely white at maturity. Pigmentation of the skin and eyes is not affected by GG. Dark skin distinguishes the gray phenotype from that of pink-skinned cremello and white horses.
Pearl is known to interact with Cream dilution to produce pseudo-double Cream dilute phenotypes including pale skin and blue/green eyes.
No true albino mutation of the color gene is known among horses, though several varieties of white horse are popularly known as albinos.
...the inability of albino animals to produce pigment stems not from an absence of melanocytes
Albinism results from a structural gene mutation at the locus that codes for tyrosinase; that is, albino animals have a genetically determined failure of tyrosine synthesis.
In the most severe form, the latter may look pink since the only pigment present is hemoglobin within the iris blood vessels