alleles
Information about alleles
For the hard rock band, see .
An allele (Pronounced: /əˈlil/) is a viable DNA (deoxyribonucleic acid) coding that occupies a given locus (position) on a chromosome. Usually alleles are sequences that code for a gene, but sometimes the term is used to refer to a non-gene sequence. An individual's genotype for that gene is the set of alleles it happens to possess. In a diploid organism, one that has two copies of each chromosome, two alleles make up the individual's genotype. The word came from Greek αλληλος = "each other".
An example is the gene for blossom colour in many species of flower — a single gene controls the colour of the petals, but there may be several different versions (or alleles) of the gene. One version might result in red petals, while another might result in white petals. The resulting colour of an individual flower will depend on which two alleles it possesses for the gene and how the two interact.
Introduction
Diploid organisms, for example, humans, have paired homologous chromosomes in their somatic cells, and these contain two copies of each gene. An organism in which the two copies of the gene are identical — that is, have the same allele — is called homozygous for that gene. An organism which has two different alleles of the gene is called heterozygous. Phenotypes (the expressed characteristics) associated with a certain allele can sometimes be dominant or recessive, but often they are neither. A dominant phenotype will be expressed when at least one allele of its associated type is present, whereas a recessive phenotype will only be expressed when both alleles are of its associated type.However, there are exceptions to the way heterozygotes express themselves in the phenotype. One exception is incomplete dominance (sometimes called blending inheritance) when alleles blend their traits in the phenotype. An example of this would be seen if, when crossing Antirrhinums — flowers with incompletely dominant "red" and "white" alleles for petal color — the resulting offspring had pink petals. Another exception is co-dominance, where both alleles are active and both traits are expressed at the same time; for example, both red and white petals in the same bloom or red and white flowers on the same plant. Codominance is also apparent in human blood types. A person with one "A" blood type allele and one "B" blood type allele would have a blood type of "AB".
A wild type allele is an allele which is considered to be "normal" for the organism in question, as opposed to a mutant allele which is usually a relatively new modification.
(Note that with the advent of neutral genetic markers, the term 'allele' is now often used to refer to DNA sequence variants in non-functional, or junk DNA. For example, allele frequency tables are often presented for genetic markers, such as the DYS markers.) Also there are many different types of alleles.
Equations
There are two equations for the frequency of two alleles of a given gene (see Hardy-Weinberg principle).Equation 1:
,
Equation 2:
where
is the frequency of one allele and
is the frequency of the other allele. Under appropriate conditions, subject to numerous limitations regarding the applicability of the Hardy-Weinberg principle,
is the population fraction that is homozygous for the
allele,
is the frequency of heterozygotes and
is the population fraction that is homozygous for the
allele.
Natural selection can act on
and
in Equation 1, and obviously affect the frequency of alleles seen in Equation 2.
Equation 2 is a consequence of Equation 1, obtained by squaring both sides and applying the binomial theorem to the left-hand side. Conversely,
implies
since
and
are positive numbers.
The following equation (commonly termed the Lee equation) can be used to calculate the number of possible genotypes in a diploid organism for a specific gene with a given number of alleles.
where
is the number of different alleles for the gene being dealt with and
is the number of possible genotypes.
For example, the human ABO blood group gene has three alleles; A (for blood group A), B (for blood group B) and i (for blood group O). As such, (using the equation) the number of possible genotypes a human may have with respect to the ABO gene are 6 (AA, Ai, AB, BB, Bi, ii). The equation does not specify the number of possible phenotypes, however. Such an equation would be quite impossible as the number of possible phenotypes varies amongst different genes and their alleles. For example, in a diploid heterozygote some genotypes may show complete dominance, incomplete dominance etc., depending of the gene involved.
Types
There are 4 different types of alleles. Dominant, recessive, codominant, and incomplete dominant. Depending on the inheritance of two alleles, a person may therefore end up having a dominant, recessive, codominant, or incomplete dominant trait. In a single-gene trait, only two alleles determine the trait. In a polygenic trait, more than two alleles control the trait.An example of a dominant and a recessive trait is the (dis)possession of a widow's peak. Those who have a widow's peak are dominant and those who do not have one are recessive.
An example of a codominant trait occurs in certain types of calves (cow's young). Some calves are known as "blue roans" for their appearance of both blue and grey hairs.
An example of an incomplete dominant trait occurs in a pink 4-o'clock flower. When a red flower (dominant) and a white flower (recessive) are crossed , those flowers with a heterozygous genotype for color are pink, showing the incomplete dominance of the red allele.
An example of multiple alleles is blood type. People have AA, BB, AB, AO, BO, or OO blood.
Genetic Disorders
Genetic disorders are normally caused by the acquisition of two recessive alleles for a single-gene trait. Genetic disorders such as these include Albinism, Cystic Fibrosis, Galactosemia, Phenylketonuria (PKU), and Tay-Sachs Disease. These two alleles are autosomal (not sex chromosomes).Some other disorders are caused by the presence of a dominant allele.
See also
- Evolution
- Genealogical DNA test
- Haplo-sufficiency
- Meiosis
- Mendelian error
- Mendelian inheritance
- Mitosis
- Punnett square
External links
References
Natioinal Geographic Society, Alton Biggs, Lucy Daniel, Edward Ortleb, Peter Rillero, Dinah Zike. "Life Science". New York, Ohio, California, Illinois: Glencoe McGraw-Hill. 2002. Hard rock is a variation of rock and roll music which has its earliest roots in mid-1960s garage and psychedelic rock. It is typified by a heavy use of distorted electric guitars, bass guitar and drums.
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The International
Phonetic Alphabet
History
Nonstandard symbols
Extended IPA
Naming conventions
IPA for English The
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Note: This page may contain IPA phonetic symbols in Unicode.
The International
Phonetic Alphabet
History
Nonstandard symbols
Extended IPA
Naming conventions
IPA for English The
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locus (plural loci) is a fixed position on a chromosome, such as the position of a gene or a biomarker (genetic marker). A variant of the DNA sequence at a given locus is called an allele. The ordered list of loci known for a particular genome is called a genetic map.
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Figure 1: A representation of a condensed eukaryotic chromosome, as seen during cell division.]] A chromosome is a single large macromolecule of DNA, and constitutes a physically organized form of DNA in a cell.
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For a non-technical introduction to the topic, see .
A gene is a locatable region of genomic sequence, corresponding to a unit of inheritance, which is associated with regulatory regions, transcribed regions and/or other functional sequence regions...... Click the link for more information.
Genotype describes the genetic constitution of an individual, that is the specific allelic makeup of an individual, usually with reference to a specific character under consideration [1].
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In evolutionary biology, homology is any similarity between characters that is due to their shared ancestry. There are examples in different branches of biology. Anatomical structures that perform the same function in different biological species and evolved from the same structure
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A somatic cell is generally taken to mean any cell forming the body of an organism: the word "somatic" is derived from the Greek word sōma (σώμα), meaning "body". Somatic cells, by definition, are not germline cells.
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Zygosity refers to the genetic condition of a zygote. In genetics, zygosity describes the similarity or dissimilarity of DNA between homologous chromosomes at a specific allelic position or gene.
Every gene in a diploid organism has two alleles at the gene's locus.
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Every gene in a diploid organism has two alleles at the gene's locus.
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Zygosity refers to the genetic condition of a zygote. In genetics, zygosity describes the similarity or dissimilarity of DNA between homologous chromosomes at a specific allelic position or gene.
Every gene in a diploid organism has two alleles at the gene's locus.
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Every gene in a diploid organism has two alleles at the gene's locus.
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phenotype describes the total physical appearance of an organism, as opposed to its genotype. This genotype-phenotype distinction was proposed by Wilhelm Johannsen in 1911 to make clear the difference between an organism's heredity and what that heredity produces.
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dominance relationship refers to how the alleles for a locus interact to produce a phenotype.
There are three main kinds of dominance relationships:
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There are three main kinds of dominance relationships:
- Simple dominance or complete dominance (simple Mendelian inheritance) over a recessive trait
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dominance relationship refers to how the alleles for a locus interact to produce a phenotype.
There are three main kinds of dominance relationships:
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There are three main kinds of dominance relationships:
- Simple dominance or complete dominance (simple Mendelian inheritance) over a recessive trait
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dominance relationship refers to how the alleles for a locus interact to produce a phenotype.
There are three main kinds of dominance relationships:
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There are three main kinds of dominance relationships:
- Simple dominance or complete dominance (simple Mendelian inheritance) over a recessive trait
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blending inheritance -- an offspring was an average of its parents. If an individual had one short parent and one tall parent, it would be of medium height. And, the offspring would pass on genes for medium sized offspring.
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dominance relationship refers to how the alleles for a locus interact to produce a phenotype.
There are three main kinds of dominance relationships:
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There are three main kinds of dominance relationships:
- Simple dominance or complete dominance (simple Mendelian inheritance) over a recessive trait
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Blood type (or blood group) is determined, in part, by the ABO blood group antigens present on red blood cells.]] A blood type (also called a blood group) is a classification of blood based on the presence or absence of inherited antigenic substances on the surface of
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Wild type, sometimes written wildtype or wild-type, is the typical form of an organism, strain, gene, or characteristic as it occurs in nature. Wild type refers to the most common phenotype in the natural population.
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mutant is an individual, organism, or new genetic character arising or resulting from an instance of mutation, which is a sudden structural change within the DNA of a gene or chromosome of an organism resulting in the creation of a new character or trait not found in the wildtype.
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A genetic marker is a known DNA sequence that can be identified by a simple assay.
It can be described as some sort of variation present can arise due to mutation or alteration in the genomic loci that can be observed.
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It can be described as some sort of variation present can arise due to mutation or alteration in the genomic loci that can be observed.
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In molecular biology, "junk" DNA is a collective label for the portions of the DNA sequence of a chromosome or a genome for which no function has yet been identified. About 80-90% of the human genome has been designated as "junk", including most sequences within introns and most
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Allele frequency is a measure of the relative frequency of an allele on a genetic locus in a population. Usually it is expressed as a proportion or a percentage. In population genetics, allele frequencies show the genetic diversity of a species population or equivalently the
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DYS is short for DNA Y-chromosome Segment, and is used to designate a segment of DNA on the Y chromosome where a sequence of nucleotides repeats. These sequences are known as short tandem repeats (STRs), and are called markers in genealogical DNA testing.
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Hardy–Weinberg principle is a relationship between the frequencies of alleles and the genotype of a population. The occurrence of a genotype, perhaps one associated with a disease, stays constant unless matings are non-random or inappropriate, or mutations accumulate.
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Hardy–Weinberg principle is a relationship between the frequencies of alleles and the genotype of a population. The occurrence of a genotype, perhaps one associated with a disease, stays constant unless matings are non-random or inappropriate, or mutations accumulate.
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Natural selection is the process by which favorable traits that are heritable become more common in successive generations of a population of reproducing organisms, and unfavorable traits that are heritable become less
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In mathematics, the binomial theorem is an important formula giving the expansion of powers of sums. Its simplest version says
whenever n is any non-negative integer, the number
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whenever n is any non-negative integer, the number
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