Genetic load
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In population genetics, genetic load or genetic burden is a measure of the cost of lost alleles due to selection (selectional load) or mutation (mutational load). It is a value in the range 0 < L < 1, where 0 represents no load. The concept was first formulated by the British population geneticist J.B.S. Haldane.[1]
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[edit] Definition
Genetic load is the reduction in selective value for a population compared to what the population would have if all individuals had the most favored genotype.[2] It is normally stated in terms of fitness as the reduction in the mean fitness for a population compared to the maximum fitness.
[edit] Mathematics
Consider a single gene locus with the alleles , which have the fitnesses and the allele frequencies respectively. Ignoring frequency-dependent selection, then genetic load (L) may be calculated as:
where wmax is the maximum value of the fitnesses and is mean fitness which is calculated as the mean of all the fitnesses weighted by their corresponding allele frequency:
where the ith allele is and has the fitness and frequency wi and pi respectively.
When the wmax = 1, then (1) simplifies to
[edit] Causes of genetic load
Load may be caused by selection and mutation.
[edit] Mutational load
Load caused by mutations is known as mutational load.
[edit] Selectional load
Selection occurs when the fitnesses of particular alleles are inequal, hence selection always exerts a load.
With directional selection, the allele frequencies will tend towards an equilibrium position with the fittest allele reaching a frequency in mutation-selection balance. As mutations are rare, this is effectively fixation. Consider two alleles and . If w1 > w2, then at equilibrium, and , hence , and .
In contrast to directional selection, heterozygote advantage always exerts a load at equilibrium.
If the mean fitness is 0, the load is equal to 1, but the population goes extinct.
[edit] Creationist criticism
Some creationists (such as Henry M. Morris) have suggested that mutational load would increase over time and thus make populations inviable. However, they ignore the effect of selection acting to weed out deleterious mutations.
[edit] References
- ^ JBS Haldane (1957). "The cost of natural selection". Journal of Genetics 55: 511-524.
- ^ JF Crow (1958). "Some possibilities for measuring selection intensities in man". Hum. Biol 30: 1-13.