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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 richness of its gene pool. Allele frequency is defined as follows:
Given the following:
- a particular chromosome locus and the gene occupying that locus
- a population of individuals carrying n loci in each of their somatic cells (e.g. two loci in the cells of diploid species, which contain two sets of chromosomes)
- a variant or allele of the gene,
Then the allele frequency is the fraction or percentage of loci that the allele occupies within the population.
For example, if the frequency of an allele is 20% in a given population, then among population members, one in five chromosomes will carry that allele. Four out of five will be occupied by other variant(s) of the gene. Note that for diploid genes the fraction of individuals that carry this allele may be nearly two in five. If the allele distributes randomly, then the binomial theorem will apply: 32% of the population will be heterozygous for the allele (i.e. carry one copy of that allele and one copy of another in each somatic cell) and 4% will be homozygous (carrying two copies of the allele). Together, this means that 36% of diploid individuals would be expected to carry an allele that has a frequency of 20%. However, alleles distribute randomly only under certain assumptions, including the absence of selection. When these conditions apply, a population is said to be in Hardy-Weinberg equilibrium.
The frequencies of all the alleles of a given gene often are graphed together as an allele frequency distribution histogram. Population genetics studies the different "forces" that might lead to changes in the distribution and frequencies of alleles -- in other words, to evolution. Besides selection, these forces include genetic drift, mutation and migration.
Calculation of allele frequencies from genotype frequenciesEdit
If , , and are the frequencies of the three genotypes at a locus with two alleles, then the frequency p of the A-allele and the frequency q of the a-allele are obtained by counting alleles. Because each homozygote AA consists only of A-alleles, and because half of the alleles of each heterozygote Aa are A-alleles, the total frequency p of A-alleles in the population is calculated as
- frequency of A
Similarly, the frequency q of the a allele is given by
- frequency of a
It would be expected that p and q sum to 1, since they are the frequencies of the only two alleles present. Indeed they do:
and from this we get:
If there are more than two different allelic forms, the frequency for each allele is simply the frequency of its homozygote plus half the sum of the frequencies for all the heterozygotes in which it appears.
It is interesting to note here that allele frequency can always be calculated from genotype frequency. The reverse, however, requires that the Hardy-Weinberg conditions of random mating apply. This is partly due to the three genotype frequencies and the two allele frequencies. It is easier to reduce from three to two.
An example populationEdit
Consider a population of ten individuals and a given locus with two possible alleles, A and a. Suppose that the genotypes of the individuals are as follows:
- AA, Aa, AA, aa, Aa, AA, AA, Aa, Aa, and AA
Then the allele frequencies of allele A and allele a are:
The effect of mutationEdit
Let ú be the mutation rate from allele A to some other allele a ( the probability that a copy of gene A will become a during the DNA replication preceding meiosis). If is the frequency of the A allele in generation t, if is the frequency of the a allele in generation t, and if there are no other causes of gene frequency change (no natural selection, for example), then the change in allele frequency in one generation is
where is the frequency of the preceding generation. This tells us that the frequency of A decreases (and the frequency of a increases) by an amount that is proportional to the mutation rate ú and to the proportion p of all the genes that are still available to mutate. Thus gets smaller as the frequency of p itself decreases, because there are fewer and fewer A alleles to mutate into a alleles. We can make an approximation that, after n generations of mutation,
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