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Tortoiseshell Cat
Tortoiseshell is a cat animal coloration, coat coloring named for its similarity to tortoiseshell material. Like calico cat, calicoes, tortoiseshell cats are almost exclusively female. Male tortoiseshells are rare and are usually sterile.Atkins (2003), p.105 Tortoiseshell cats, or torties, combine two colors other than white, either closely mixed or in larger patches. The colors are often described as red and black, but the "red" patches can instead be orange, yellow, or cream, and the "black" can instead be chocolate, gray, tabby cat, tabby, or blue. Tortoiseshell cats with the tabby cat, tabby pattern as one of their colors are sometimes referred to as torbies or torbie cats. "Tortoiseshell" is typically reserved for particolored cats with relatively small or no white markings. Those that are predominantly white with tortoiseshell patches are described as tricolor, tortoiseshell-and-white (in the United Kingdom), or calico cat, calico (in Canada and the United States). Cats wi ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cat Coat Genetics
Cat coat genetics determine the coloration, pattern, length, and texture of feline fur. Understanding how can be challenging because many genes are involved. 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 Siberian cat, Siberian could wear point coloration, the stereotypical coat of a Siamese cat, Siamese. Solid colors Eumelanin The browning gene ''B/b/bl'' codes for TYRP1 (), an enzyme involved in the metabolic pathway for eumelanin pigment production. Its dominant form, ''B'', will produce black eumelanin. It has two recessive variants, ''b'' (chocolate) and ''bl'' (cinnamon), with ''bl'' being recessive to both ''B'' and ''b''. Chocolate is a rich dark brown color, and is referred to as chestnut in some breeds. Cinnamon is a light reddish brown, but is sometimes not reddish at all. Sex-linked orange/red The sex-linked ' ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Cat Colors
Cat coat genetics determine the coloration, pattern, length, and texture of feline fur. Understanding how can be challenging because many genes are involved. 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 Siberian could wear point coloration, the stereotypical coat of a Siamese. Solid colors Eumelanin The browning gene ''B/b/bl'' codes for TYRP1 (), an enzyme involved in the metabolic pathway for eumelanin pigment production. Its dominant form, ''B'', will produce black eumelanin. It has two recessive variants, ''b'' (chocolate) and ''bl'' (cinnamon), with ''bl'' being recessive to both ''B'' and ''b''. Chocolate is a rich dark brown color, and is referred to as chestnut in some breeds. Cinnamon is a light reddish brown, but is sometimes not reddish at all. Sex-linked orange/red The sex-linked ''Orange'' locus, ''O/o'', ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
X Chromosome
The X chromosome is one of the two sex-determining chromosomes (allosomes) in many organisms, including mammals (the other is the Y chromosome), and is found in both males and females. It is a part of the XY sex-determination system and XO sex-determination system. The X chromosome was named for its unique properties by early researchers, which resulted in the naming of its counterpart Y chromosome, for the next letter in the alphabet, following its subsequent discovery. Discovery It was first noted that the X chromosome was special in 1890 by Hermann Henking in Leipzig. Henking was studying the testicles of ''Pyrrhocoris'' and noticed that one chromosome did not take part in meiosis. Chromosomes are so named because of their ability to take up staining (''chroma'' in Greek means ''color''). Although the X chromosome could be stained just as well as the others, Henking was unsure whether it was a different class of object and consequently named it ''X element'', which later be ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Mosaic (genetics)
Mosaicism or genetic mosaicism is a condition in multicellular organisms in which a single organism possesses more than one genetic line as the result of genetic mutation. This means that various genetic lines resulted from a single fertilized egg. Genetic mosaics may often be confused with chimerism, in which two or more genotypes arise in one individual similarly to mosaicism. In chimerism, though, the two genotypes arise from the fusion of more than one fertilized zygote in the early stages of embryonic development, rather than from a mutation or chromosome loss. Genetic mosaicism can result from many different mechanisms including chromosome nondisjunction, anaphase lag, and endoreplication. Anaphase lagging is the most common way by which mosaicism arises in the preimplantation embryo. Mosaicism can also result from a mutation in one cell during development, in which case the mutation will be passed on only to its daughter cells (and will be present only in certain adult ce ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Chimera (genetics)
A genetic chimerism or chimera ( ) is a single organism composed of cells with more than one distinct genotype. In animals, this means an individual derived from two or more zygotes, which can include possessing blood cells of different blood types, subtle variations in form (phenotype) and, if the zygotes were of differing sexes, then even the possession of both female and male sex organs. Animal chimeras are produced by the merger of two (or more) embryos. In plant chimeras, however, the distinct types of tissue may originate from the same zygote, and the difference is often due to mutation during ordinary cell division. Normally, genetic chimerism is not visible on casual inspection; however, it has been detected in the course of proving parentage. Another way that chimerism can occur in animals is by organ transplantation, giving one individual tissues that developed from a different genome. For example, transplantation of bone marrow often determines the recipient's en ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Klinefelter Syndrome
Klinefelter syndrome (KS), also known as 47,XXY, is an aneuploid genetic condition where a male has an additional copy of the X chromosome. The primary features are infertility and small, poorly functioning testicles. Usually, symptoms are subtle and subjects do not realize they are affected. Sometimes, symptoms are more evident and may include weaker muscles, greater height, poor motor coordination, less body hair, breast growth, and less interest in sex. Often, these symptoms are noticed only at puberty. Intelligence is usually normal, but reading difficulties and problems with speech are more common. Klinefelter syndrome occurs randomly. The extra X chromosome comes from the father and mother nearly equally. An older mother may have a slightly increased risk of a child with KS. The syndrome is defined by the presence of at least one extra X chromosome in addition to a Y chromosome yielding a total of 47 or more chromosomes rather than the usual 46. KS is diagnosed by t ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Sex-determination System
A sex-determination system is a biological system that determines the development of sexual characteristics in an organism. Most organisms that create their offspring using sexual reproduction have two sexes. In some species there are hermaphrodites. There are also some species that are only one sex due to parthenogenesis, the act of a female reproducing without fertilization. In some species, sex determination is genetic: males and females have different alleles or even different genes that specify their sexual morphology. In animals this is often accompanied by chromosomal differences, generally through combinations of XY, ZW, XO, ZO chromosomes, or haplodiploidy. The sexual differentiation is generally triggered by a main gene (a "sex locus"), with a multitude of other genes following in a domino effect. In other cases, sex of a fetus is determined by environmental variables (such as temperature). The details of some sex-determination systems are not yet fully underst ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Turkish Van
The Turkish Van (pronounced Von) is a naturally occurring breed of domestic cat that originated in the Lake Van area of modern-day Turkey, part of Armenian Highlands. The Van is classified as a semi-long hair, but it has two lengths of hair, determined by season. In the winter, the hair is thick and long. In the summer, the hair sheds to leave a short light coat. Both coat lengths are typified as being as soft as cashmere, down to the root. There is no evident undercoat on the Van, only one coat. The breed is rare, This source, in some places, conflates the Turkish Van breed and the Van cat landrace. and is distinguished by the Van pattern (named after the breed), where the color is restricted to the head and the tail, and the rest of the cat is white; this is due to the expression of the piebald white spotting gene, a type of partial leucism. A Turkish Van may have blue or amber eyes, or be odd-eyed (having one eye of each colour). The breed has been claimed to be descended fro ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Bicolor Cat , an early method of filming in color
{{disambiguation ...
Bicolor or bicolour may refer to: * Bicolour (flag), a flag of two color bands ** Bicolour, the flag of Haiti ** in the widest sense, any flag design with two colors, see List of flags by number of colors#2 * Bicolor cat, or piebald cat, a cat with white fur and fur of some other color See also * * , including a number of biological species * Two Colours (other) * Bipack color In bipack color photography for motion pictures, two strips of black-and-white 35 mm film, running through the camera emulsion to emulsion, are used to record two regions of the color spectrum, for the purpose of ultimately printing the images, ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Melanocytes
Melanocytes are melanin-producing neural crest-derived cells located in the bottom layer (the stratum basale) of the skin's epidermis, the middle layer of the eye (the uvea), the inner ear, vaginal epithelium, meninges, bones, and heart. Melanin is a dark pigment primarily responsible for skin color. Once synthesized, melanin is contained in special organelles called melanosomes which can be transported to nearby keratinocytes to induce pigmentation. Thus darker skin tones have more melanosomes present than lighter skin tones. Functionally, melanin serves as protection against UV radiation. Melanocytes also have a role in the immune system. Function Through a process called melanogenesis, melanocytes produce melanin, which is a pigment found in the skin, eyes, hair, nasal cavity, and inner ear. This melanogenesis leads to a long-lasting pigmentation, which is in contrast to the pigmentation that originates from oxidation of already-existing melanin. There are both ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Barr Body
A Barr body (named after discoverer Murray Barr) or X-chromatin is an inactive X chromosome in a cell with more than one X chromosome, rendered inactive in a process called lyonization, in species with XY sex-determination (including humans). The Lyon hypothesis states that in cells with multiple X chromosomes, all but one are inactivated during mammalian embryogenesis. This happens early in embryonic development at random in mammals,Brown, C.J., Robinson, W.P., (1997), XIST Expression and X-Chromosome Inactivation in Human Preimplantation Embryos ''Am. J. Hum. Genet.'' 61, 5–8Full Text PDF except in marsupials and in some extra-embryonic tissues of some placental mammals, in which the X chromosome from the sperm is always deactivated. In humans with euploidy, a genotypical female (46, XX karyotype) has one Barr body per somatic cell nucleus, while a genotypical male (46, XY) has none. The Barr body can be seen in the interphase nucleus as a darkly staining small mass in ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
X-inactivation
X-inactivation (also called Lyonization, after English geneticist Mary Lyon) is a process by which one of the copies of the X chromosome is inactivated in therian female mammals. The inactive X chromosome is silenced by being packaged into a transcriptionally inactive structure called heterochromatin. As nearly all female mammals have two X chromosomes, X-inactivation prevents them from having twice as many X chromosome gene products as males, who only possess a single copy of the X chromosome (see dosage compensation). The choice of which X chromosome will be inactivated in a particular embryonic cell is random in placental mammals such as humans, but once an X chromosome is inactivated it will remain inactive throughout the lifetime of the cell and its descendants in the organism (its cell line). The result is that the choice of inactivated X chromosome in all the cells of the organism is a random distribution, often with about half the cells having the paternal X chromos ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
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