Слайд 2Genetic load
Genetic load: the extent to which the fitness of an
individual is below the optimum for the population as a whole due to the deleterious alleles that the individual carries in its genome.
Genetic load : The average number of lethal mutations per individual in a population. Such mutations result in the premature death of the organisms carrying them.
Слайд 3Genetic load: the difference between the average fitness of the population and
the fitness of the best genotype. It measures the probability of selective death of an individual in a population.
W = average fitness
Genetic load (L) = 1 - W
Слайд 4Types of Genetic Load
Three main kinds of genetic load may be recognized:
A.Input
Load: in which inferior alleles are introduced into the gene pool of a population either by mutation or immigration;
B. Balanced Load: which is created by selection favouring allelic or genetic combinations that, by segregation and recombination, form inferior genotypes every generation; and
Слайд 5C. Substitutional Load: Which is generated by selection favouring the replacement of
an existing allele by a new allele.
Originally called the ‘cost of natural selection’ by the geneticist J. B. S. Haldane, substitutional load is the genetic load associated with transient polymorphism.
The term ‘genetic load’ was originally coined by H. J. Muller in 1950
Слайд 7Genetic load an Example…
Selective death (or genetic death): the chance that an
individual will die without reproducing as a consequence of natural selection. [e.g.,15% of offspring in above]
Слайд 8Causes of Genetic Load
1.Deleterious mutation
2.Beneficial mutation
3.Inbreeding
4.Recombination/segregation load
Слайд 9DELETERIOUS MUTATIONS
Deleterious mutation load is the main contributing factor to genetic load
overall.
Most mutations are neutral or slightly deleterious, and occur at a constant rate.
The Haldane-Muller theorem of mutation–selection balance says that the load depends only on the deleterious mutation rate and not on the selection coefficient.
High load can lead to a small population size, which in turn increases the accumulation of mutation load, culminating in extinction via mutational meltdown.
Слайд 10Beneficial mutation
New beneficial mutations create fitter genotypes than those previously present in
the population.
When load is calculated as the difference between the fittest genotype present and the average, this creates a substitutional load.
The difference between the theoretical maximum (which may not actually be present) and the average is known as the "lag load.
Слайд 12Inbreeding
Inbreeding increases homozygosity.
In the short run, an increase in inbreeding increases
the probability with which offspring get two copies of a recessive deleterious alleles, lowering fitnesses via inbreeding depression.
In a species that habitually inbreeds, e.g. through self-fertilization, recessive deleterious alleles are purged.
Слайд 13Recombination/segregation load
Combinations of alleles that have evolved to work well together may
not work when recombined with a different suite of coevolved alleles, leading to outbreeding depression.
Segregation load is the presence of underdominant heterozygotes (i.e. heterozygotes that are less fit than either homozygote).
Слайд 14Recombination load arises through unfavorable combinations across multiple loci that appear when
favorable linkage disequilibria are broken down.
Recombination load can also arise by combining deleterious alleles subject to synergistic epistasis, i.e. whose damage in combination is greater than that predicted from considering them in isolation.
Слайд 16Genetic load: segregational
Segregational load is a big problem for the balance school:
Well
known examples exist; Haemoglobin, MHC locus, etc.
Слайд 17There is a cost to selection, in genetic death, during this time
period
Слайд 18 Migration load
Migration load is the result of nonnative organisms that aren’t adapted
to a particular environment coming into that environment.
If they breed with individuals who are adapted to that environment, their offspring will not be as fit as they would have been if both of their parents had been adapted to that particular environment.
Слайд 19“It is altogether unlikely that two genes would have identical selective values
under all the conditions under which they may coexist in a population. … cases of neutral polymorphism do not exist … it appears probable that random fixation is of negligible evolutionary importance”
-------Ernst Mayr
Слайд 20Defining Directional Section
Directional selection: selection that favours the phenotype at an extreme
of the range of phenotypes
Directional selection: can be subdivided into two broad categories.
1.Positive Darwinian selection
2.Negative Darwinian selection
Слайд 21Defining two types directional selection
Type 1:
Positive Darwinian selection: directional selection for
fixation of a new and beneficial mutation in a population.
Слайд 22 Type 2:
Negative Darwinian selection: directional selection for removal of a new
and deleterious mutation from a population.
Negative selection: same as “negative Darwinian selection”.
Purifying election: same as negative selection.