Fixation (population genetics)

In population genetics, fixation is the change in a gene pool from a situation where there exists at least two variants of a particular gene (allele) in a given population to a situation where only one of the alleles remains. That is, the allele becomes fixed. [1] In the absence of mutation or heterozygote advantage, any allele must eventually either be lost completely from the population, or fixed, i.e. permanently established at 100% frequency in the population.[2] Whether a gene will ultimately be lost or fixed is dependent on selection coefficients and chance fluctuations in allelic proportions.[3] Fixation can refer to a gene in general or particular nucleotide position in the DNA chain (locus).

In the process of substitution, a previously non-existent allele arises by mutation and undergoes fixation by spreading through the population by random genetic drift or positive selection. Once the frequency of the allele is at 100%, i.e. being the only gene variant present in any member, it is said to be "fixed" in the population.[1]

Similarly, genetic differences between taxa are said to have been fixed in each species.

  1. ^ a b Arie Zackay (2007). Random Genetic Drift & Gene Fixation (PDF). Archived from the original (PDF) on 2016-03-04. Retrieved 2013-08-29.
  2. ^ Kimura, Motoo; Ohta, Tomoko (26 July 1968). "The average number of generations until fixation of a mutant gene in a finite population". Genetics. 61 (3): 763–771. doi:10.1093/genetics/61.3.763. PMC 1212239. PMID 17248440.
  3. ^ Kimura, Motoo (1983). The Neutral Theory of Molecular Evolution. The Edinburgh Building, Cambridge: Cambridge University Press. ISBN 978-0-521-23109-1. Retrieved 16 November 2014.

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