The disappearing blonde gene was a hoax claiming a scientific study had estimated that natural blonds would become extinct, repeated as fact in reputable media such as the BBC and The Sunday Times between 2002 and 2006. The hoax claimed that, because the allele for the genes for hair colour is recessive, blond hair would become less common as people with dominant non-blond hair alleles had offspring with people with the recessive alleles, even though such a pairing would retain one copy of the blond allele in the genome of the offspring. Claims that blond hair would disappear have been made since 1865. [2]
Several reports erroneously claimed that the World Health Organization (WHO) had published a report claiming that people with blond hair "will become extinct by 2202". Neither the WHO nor any reputable expert had issued such a report, and the WHO asked those commenting on the alleged report to retract. [3]
In 2002, BBC News reported that unnamed German experts concluded that blond hair would disappear within 200 years since the gene causing blond hair is recessive. According to the German experts, the recessive blond allele is rare in nations of mixed heritage (for example, the United States, Canada, Argentina, Brazil, New Zealand and Australia). In the BBC article Prof. Jonathan Rees of the University of Edinburgh cast doubt on the story—he was quoted as saying "The frequency of blondes may drop but they won't disappear." [4]
In 2006 the hoax was mentioned by The Sunday Times when reporting on the publication of a hypothesis of the origins of blonde hair [5] and La Repubblica : "According to the WHO study, the last natural blond is likely to be born in Finland during 2202." It once again traveled quickly across the World Wide Web. [6] The hoax has also been featured on the "Threat-Down" segment of the satirical television show The Colbert Report on March 6, 2006, where Stephen Colbert suggested a selective breeding program to save blonds. [7]
The extinction hoax is based on a misinterpretation of recessiveness in genetics. [4] In reality, gene frequency is stable unless there is selection for or against them, [8] which does not appear to be the case for blonde hair. [4] In large populations, even extremely rare genes will persist at stable levels over long periods of time. It also does not matter whether a gene is dominant or recessive. Genes disappear if the population is very small (drift) or if they confer a disadvantage (selection). [8]
The Melanocortin 1 receptor gene is known to affect human hair colour, and alleles on that gene associated with blond hair are generally recessive to alleles associated with darker hair colours. However, there is no single allele that codes for blonde hair colour, and environmental factors can also determine whether blonde or brown hair colour is expressed in an individual. Additionally, several factors involving determination of human hair colour are still not fully understood by geneticists. [1]
An allele, or allelomorph, is a variant of the sequence of nucleotides at a particular location, or locus, on a DNA molecule.
The genotype of an organism is its complete set of genetic material. Genotype can also be used to refer to the alleles or variants an individual carries in a particular gene or genetic location. The number of alleles an individual can have in a specific gene depends on the number of copies of each chromosome found in that species, also referred to as ploidy. In diploid species like humans, two full sets of chromosomes are present, meaning each individual has two alleles for any given gene. If both alleles are the same, the genotype is referred to as homozygous. If the alleles are different, the genotype is referred to as heterozygous.
Mendelian inheritance is a type of biological inheritance following the principles originally proposed by Gregor Mendel in 1865 and 1866, re-discovered in 1900 by Hugo de Vries and Carl Correns, and later popularized by William Bateson. These principles were initially controversial. When Mendel's theories were integrated with the Boveri–Sutton chromosome theory of inheritance by Thomas Hunt Morgan in 1915, they became the core of classical genetics. Ronald Fisher combined these ideas with the theory of natural selection in his 1930 book The Genetical Theory of Natural Selection, putting evolution onto a mathematical footing and forming the basis for population genetics within the modern evolutionary synthesis.
In genetics, dominance is defined as the interactions between alleles at the same locus on homologous chromosomes and the associated phenotype. In the case of complete dominance, one allele in a heterozygote individual completely overrides or masks the phenotypic contribution of the other allele. The overriding allele is referred to as dominant and the masked one recessive. Complete dominance, also referred to as Mendelian inheritance, follow Mendel's laws of segregation. The first law states that each allele in a pair of genes is separated at random and have an equal probability of being transferred to the next generation, while the second law states that the distribution of allele variants is done independently of each other. However, this is not always the case as not all genes segregate independently and violations of this law are often referred to as "non-Mendelian inheritance".
Red hair, also known as orange hair or ginger hair, is a human hair color found in 1–2% of the world population, appearing with greater frequency (2–6%) among people of Northern or Northwestern European ancestry and lesser frequency in other populations. It is most common in individuals homozygous for a recessive allele on chromosome 16 that produces an altered version of the MC1R protein.
The Punnett square is a square diagram that is used to predict the genotypes of a particular cross or breeding experiment. It is named after Reginald C. Punnett, who devised the approach in 1905. The diagram is used by biologists to determine the probability of an offspring having a particular genotype. The Punnett square is a tabular summary of possible combinations of maternal alleles with paternal alleles. These tables can be used to examine the genotypical outcome probabilities of the offspring of a single trait (allele), or when crossing multiple traits from the parents. The Punnett square is a visual representation of Mendelian inheritance. For multiple traits, using the "forked-line method" is typically much easier than the Punnett square. Phenotypes may be predicted with at least better-than-chance accuracy using a Punnett square, but the phenotype that may appear in the presence of a given genotype can in some instances be influenced by many other factors, as when polygenic inheritance and/or epigenetics are at work.
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.
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.
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.
Sex linked describes the sex-specific reading patterns of inheritance and presentation when a gene mutation (allele) is present on a sex chromosome (allosome) rather than a non-sex chromosome (autosome). In humans, these are termed X-linked recessive, X-linked dominant and Y-linked. The inheritance and presentation of all three differ depending on the sex of both the parent and the child. This makes them characteristically different from autosomal dominance and recessiveness.
In genetics, a reciprocal cross is a breeding experiment designed to test the role of parental sex on a given inheritance pattern. All parent organisms must be true breeding to properly carry out such an experiment. In one cross, a male expressing the trait of interest will be crossed with a female not expressing the trait. In the other, a female expressing the trait of interest will be crossed with a male not expressing the trait. It is the cross that could be made either way or independent of the sex of the parents. For example, suppose a biologist wished to identify whether a hypothetical allele Z, a variant of some gene A, is on the male or female sex chromosome. They might first cross a Z-trait female with an A-trait male and observe the offspring. Next, they would cross an A-trait female with a Z-trait male and observe the offspring. Via principles of dominant and recessive alleles, they could then make an inference as to which sex chromosome contains the gene Z, if either in fact did.
Under the law of dominance in genetics, an individual expressing a dominant phenotype could contain either two copies of the dominant allele or one copy of each dominant and recessive allele. By performing a test cross, one can determine whether the individual is heterozygous or homozygous dominant.
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.
The German Rex is a breed of domestic cat.
Genetics is the study of genes and tries to explain what they are and how they work. Genes are how living organisms inherit features or traits from their ancestors; for example, children usually look like their parents because they have inherited their parents' genes. Genetics tries to identify which traits are inherited and to explain how these traits are passed from generation to generation.
Lethal alleles are alleles that cause the death of the organism that carries them. They are usually a result of mutations in genes that are essential for growth or development. Lethal alleles may be recessive, dominant, or conditional depending on the gene or genes involved.
The science of rosy-faced lovebird colour genetics deals with the heredity of colour variation in the feathers of the species known as Agapornis roseicollis, commonly known as the rosy-faced lovebird or peach-faced lovebird.
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.
Roan is a horse coat color pattern characterized by an even mixture of colored and white hairs on the body, while the head and "points"—lower legs, mane, and tail—are mostly solid-colored. Horses with roan coats have white hairs evenly intermingled throughout any other color. The head, legs, mane, and tail have fewer scattered white hairs or none at all. The roan pattern is dominantly inherited, and is found in many horse breeds. While the specific mutation responsible for roan has not been exactly identified, a DNA test can determine zygosity for roan in several breeds. True roan is always present at birth, though it may be hard to see until after the foal coat sheds out. The coat may lighten or darken from winter to summer, but unlike the gray coat color, which also begins with intermixed white and colored hairs, roans do not become progressively lighter in color as they age. The silvering effect of mixed white and colored hairs can create coats that look bluish or pinkish.
Flaxen is a genetic trait in which the mane and tail of chestnut-colored horses are noticeably lighter than the body coat color, often a golden blonde shade. Manes and tails can also be a mixture of darker and lighter hairs. Certain horse breeds such as the Haflinger carry flaxen chestnut coloration as a breed trait. It is seen in chestnut-colored animals of other horse breeds that may not be exclusively chestnut.