Hardy-Weinberg Equation (Edexcel International A Level Biology): Revision Note
Changes in Allele Frequency
Hardy-Weinberg Principle
The Hardy-Weinberg principle states that if certain conditions are met, the allele frequencies of a gene within a population will not change from one generation to the next
There are several conditions or assumptions that must be met for the Hardy-Weinberg principle to hold true:
Mating must be random between individuals
The population is infinitely large
There is no migration, mutation or natural selection
The Hardy-Weinberg equation allows for the calculation of allele and genotype frequencies within populations
It also allows for predictions to be made about how these frequencies will change in future generations
If the allele frequencies in a population change over time, then it means that migration, mutation or natural selection has happened
Hardy-Weinberg calculations
If the phenotype of a trait in a population is determined by a single gene with only two alleles (we will use B / b as examples throughout this section), then the population will consist of individuals with three possible genotypes:
Homozygous dominant (BB)
Heterozygous (Bb)
Homozygous recessive (bb)
When using the Hardy-Weinberg equation, the frequency of a genotype is represented as a proportion of the population
For example, the BB genotype could be 0.40
Whole population = 1
The letter p represents the frequency of the dominant allele (B)
The letter q represents the frequency of the recessive allele (b)
As there are only two alleles at a single gene locus for this phenotypic trait in the population:
p + q = 1
The chance of an individual being homozygous dominant is p2
In this instance, the offspring would inherit dominant alleles from both parents ( p x p = p2 )
The chance of an individual being heterozygous is 2pq
Offspring could inherit a dominant allele from the father and a recessive allele from the mother ( p x q ) or offspring could inherit a dominant allele from the mother and a recessive allele from the father ( p x q ) = 2pq
The chance of an individual being homozygous recessive is q2
In this instance, the offspring would inherit recessive alleles from both parents ( q x q = q2 )
As these are all the possible genotypes of individuals in the population, the following equation can be constructed:
p2 + q2 + 2pq = 1
Worked Example
In a population of birds, 10% of the individuals exhibit the recessive phenotype of white feathers. Calculate the frequencies of all genotypes.
Solution:
We will use F / f to represent dominant and recessive alleles for feather colour
Those with the recessive phenotype must have the homozygous recessive genotype, ff
Therefore q2 = 0.10 (as 10% of the individuals have the recessive phenotype and q2 represents this)
To calculate the frequencies of the homozygous dominant ( p2 ) and heterozygous ( 2pq ):
Step 1: Find q
Step 2: Find p (the frequency of the dominant allele F). If q = 0.32, and p + q = 1
p + q = 1
p = 1 - 0.32
p = 0.68
Step 3: Find p2 (the frequency of homozygous dominant genotype)
0.682 = 0.46
p2 = 0.46
Step 4: Find 2pq = 2 x (p) x (q)
2 x (0.68) x (0.32)
= 0.44
Step 5: Check calculations by substituting the values for the three frequencies into the equation; they should add up to 1
p2 + 2pq + q2 = 1
0.46 + 0.44 + 0.10 = 1
In summary:
Allele frequencies:
p = F = 0.68
q = f = 0.32
Genotype frequencies:
p2 = FF = 0.46
q2 = ff = 0.10
2pq = Ff = 0.44
Examiner Tips and Tricks
When you are using Hardy-Weinberg equations, start your calculations by determining the proportion of individuals that display the recessive phenotype - you will always know the genotype for this: homozygous recessive. Remember that the dominant phenotype is seen in both homozygous dominant, and heterozygous individuals. Also, don’t mix up the Hardy-Weinberg equations with the Hardy-Weinberg principle. The equations are used to estimate the allele and genotype frequencies in a population. The principle suggests that there is an equilibrium between allele frequencies and there is no change in this between generations.
Reasons for Changes in Allele Frequency
Mutations
Organisms of the same species will have very similar genotypes, but two individuals (even twins) will have differences between their DNA base sequences
Considering the size of genomes, these differences are small between individuals of the same species
The small differences in DNA base sequences between individual organisms within a species population is called genetic variation
Genetic variation is transferred from one generation to the next and it generates phenotypic variation within a species population
The primary source of genetic variation is mutation (changes in the DNA base sequence)
Mutation results in the generation of new alleles
The new allele may be advantageous, disadvantageous or have no apparent effect on phenotype
New alleles are not always seen in the individual that they first occur in
They can remain hidden (not expressed) within a population for several generations before they contribute to phenotypic variation
Natural selection
Variation exists within a species population
This means that some individuals within the population possess different phenotypes (due to genetic variation in the alleles they possess; remember members of the same species will have the same genes)
Environmental factors affect the chance of survival of an organism; they, therefore, act as a selection pressure
Selection pressures increase the chance of individuals with a specific phenotype surviving and reproducing over others
The individuals with the favoured phenotypes are described as having a higher fitness
The fitness of an organism is defined as its ability to survive and pass on its alleles to offspring
Organisms with higher fitness possess adaptations that make them better suited to their environment
When selection pressures act over several generations of a species, they can cause a change in the allele frequency and the phenotype frequency in a population through natural selection
Natural selection is the process by which individuals with a fitter phenotype are more likely to survive and pass on their alleles to their offspring so that the advantageous alleles increase in frequency over time and generations
An example of natural selection in rabbits
Variation in fur colour exists within rabbit populations
At a single gene locus, normal brown fur is produced by a dominant allele whereas white fur is produced by a recessive allele in a homozygous individual
Rabbits have natural predators like foxes which act as a selection pressure
Rabbits with a white coat do not camouflage as well as rabbits with brown fur, meaning predators are more likely to see white rabbits when hunting
As a result, rabbits with white fur are less likely to survive than rabbits with brown fur
The rabbits with brown fur have a selection advantage, so they are more likely to survive to reproductive age and be able to pass on their alleles to their offspring
Over many generations, the frequency of alleles for brown fur will increase and the frequency of alleles for white fur will decrease
Selective pressure acting on a rabbit population for one generation. Predation by foxes causes the frequency of brown fur alleles in rabbits to increase and the frequency of white fur alleles in rabbits to decrease
Reproductive Isolation
Organisms that belong to the same species share the same characteristics and are able to produce fertile offspring
Reproductive isolation occurs when changes in the alleles and phenotypes of some individuals in a population prevent them from successfully breeding with other individuals in the population that don't have these changed alleles or phenotypes
Examples of allele or phenotype changes that can lead to reproductive isolation include:
Seasonal changes - some individuals in a population may develop different mating or flowering seasons (becoming sexually active at different times of the year) to the rest of the population (i.e their reproductive timings no longer match up)
Mechanical changes - some individuals in a population may develop changes in their genitalia that prevent them from mating successfully with individuals of the opposite sex (i.e. their reproductive body parts no longer match up)
Behavioural changes - some individuals in a population may develop changes in their courtship behaviours, meaning they can no longer attract individuals of the opposite sex for mating (i.e. their methods of attracting a mate are no longer effective)
These changes could be brought about due to geographical barriers isolating populations or random mutations producing new, different alleles in a population
Speciation
Speciation can occur when populations of a species become separated from each other by geographical barriers
The barrier could be natural like a body of water, or a mountain range
It can also be man-made, like a motorway
This creates two populations of the same species who are reproductively isolated from each other, and as a result, no genetic exchange can occur between them
If there are sufficient selection pressures acting to change the gene pools (and allele frequencies) within both populations then eventually these populations will diverge and form separate species
The changes in the alleles/genes of each population will affect the phenotypes present in both populations
Random mutations within each population will also change allele frequencies in each
Over time, the two populations may begin to differ physiologically, behaviourally and anatomically (structurally)
This type of speciation is known as allopatric speciation
Allopatric speciation occurring due to geographical isolation of two populations of the same species
Sometimes populations of the same species live in the same geographical area but they become separated from each other by ecological or behavioural means
An example of ecological separation is populations that live in different environments within the same area e.g. plants growing in soil with different pH levels may flower at different times from each other causing reproductive isolation
This type of speciation that occurs without the presence of a geographical barrier is known as sympatric speciation
Reproductive separation due to behavioural changes that resulted in sympatric speciation occurring
Population bottlenecks
A large population is required for the maintenance of a diverse gene pool
Sometimes dramatic events occur (such as natural disasters or disease) that decrease the size of a population dramatically
This is known as a population bottleneck
It can lead to a significant decrease in the size of the gene pool of the population and will have a dramatic effect on the allele frequencies as a result thereof
The remaining population will be more susceptible to the loss of alleles and the effects of mutations will be magnified in the new population
An example is the cheetah which survived a near-extinction event in the past
Only a few individuals remained and as a result the genetic diversity of all living cheetahs are very low
This makes them very vulnerable to disease or environmental changes
A population bottleneck in the past has dramatically decreased the genetic variation in cheetahs populations
The Founder effect
This refers to the loss of genetic variation if a new population is formed by a small number of individuals that left the main population
Since the initial gene pool is small, it is unlikely that it will contain the genetic variation of the original population that the individuals came from
Should any of these individuals carry unusual mutations in their genome, these will appear more frequently in the new population
An example of this is the unusually high occurrence of Ellis-van Creveld syndrome (a type of dwarfism) among the Amish community in the USA
This was the result of a few individuals that were heterozygous for the recessive allele that formed part of the founding Amish population
The Founder effect can amplify the occurrence of genetic mutations in a population due to the small gene pool of the founding members
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