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Example Questions
Example Question #12 : Population Genetics And Hardy Weinberg
Cystic fibrosis is an autosomal recessive disease. In a population of one hundred individuals, twenty-five are found to have the disease. Assuming Hardy-Weinberg equilibrium, what is the percent of the population that are carriers for cystic fibrosis?
More information is needed
The Hardy-Weinberg formulas tell us that and , where is the dominant allele frequency and is the recessive allele frequency. is the frequency of homozygous dominant individuals in a population, is the frequency of heterozygous individuals, and is the frequency of homozygous recessive individuals.
In the question, we are told that 25 people out of 100 are homozygous recessive, meaning that .
Using this, we can find that .
If , and , then .
We are looking for the frequency of heterozygous individuals ().
50% of the population will be heterozygous (carriers) for the trait.
Example Question #11 : Population Genetics And Hardy Weinberg
In a population that is in Hardy-Weinberg equilibrium there is a gene that has only two alleles. If the dominant gene accounts for 70% of the gene pool, what percentage of the population is heterozygous for the trait?
42%
49%
58%
21%
42%
When a population is in Hardy-Weinberg equilibrium, we can predict the genotypic frequencies found in the population using the equation , where is the frequency of the dominant allele, and is the frequency of the recessive allele. Since and account for the homozygotes in the population, we can find the frequency of the heterozygotes using the portion of the equation. We can first solve for using the relationship .
Example Question #94 : Genetics
In a population that is in Hardy-Weinberg equilibrium, there is a gene that has only two alleles that codes for the color of the organism. Which of the following scenarios would not disrupt the Hardy-Weinberg equilibrium of the population?
A massive plague destroys 80% of the population
One specific color is able to survive better in the population's present environment
All color variations in the population have separate niches which allow them to thrive equally
Organisms begin to mate with partners that are the same color as themselves
All color variations in the population have separate niches which allow them to thrive equally
Hardy-Weinberg equilibrium is dependent on five key conditions:
1. The population is very large.
2. Mutations are in equilibrium (no net mutation rate).
3. There is no immigration/emigration that alters the gene pool ratios.
4. There is random mating.
5. There is no selection for the fittest organism taking place in the population.
If any of these conditions are violated in a population, Hardy-Weinberg equilibrium will be disrupted.
Example Question #1161 : Mcat Biological Sciences
75% of a given population test positive for Rhesus (Rh) factor antibodies. Given that blood type Rh+ is a dominant allele, what percentage of this population is homozygous?
We must know the total population size to solve
This question is testing your knowledge of blood types and of the Hardy-Weinberg equations. Let's first evaluate the blood type portion of the question.
Rh-positive individuals will produce Rh factor. This molecule is an antigen. The given percentage refers to the number of individuals that produce antibodies to the Rh antigen. We can conclude that 75% of the population must be Rh-negative, since they produce antibodies against Rh factor; thus, 75% of the population must be homozygous recessive, since Rh-positive is a dominant allele.
Using this information, we can apply the Hardy-Weinberg equations:
We know that 75% of the population is homozygous recessive, which corresponds to the term in the second Hardy-Weinberg equation.
Use this value to solve for the dominant allele frequency.
The total percentage of the population that is homozygous will be given by the sum of the and terms in the Hardy-Weinberg equation.
Example Question #96 : Genetics
9% of a population of mice suffer from muscle spasms due to an autosomal recessive disease. What percentage of the population are carriers for the disease?
This question requires application of the two Hardy-Weinberg equations:
We know that the disease is autosomal recessive, which means that affected individuals must be homozygous. The frequency of the homozygous recessive genotype is given by the term in the second Hardy-Weinberg equation. We can use the given genotype frequency to solve for the recessive allele frequency.
Use the first Hardy-Weinberg equation to determine the dominant allele frequency.
The frequency of the heterozygous genotype (carriers) is given by the term of the second Hardy-Weinberg equation. Use the values of the allele frequencies to calculate this term.
Example Question #1162 : Mcat Biological Sciences
In a population of a particular island, 64% of individuals have a homozygous recessive genotype. Assuming the population correlates with Hardy-Weinberg principles, what percentage of individuals in the next generation will be heterozygous?
Use equations p + q = 1 and p2 + 2pq + q2 = 1.
If 64% is homozygous recessive genotype, then q2 = 0.64.
Then solve for p and q.
q = 0.8 and p = 0.2. The frequency of heterozygous individuals is 2pq or 2(0.2)(0.8) = 0.32
Example Question #1165 : Mcat Biological Sciences
A certain island-nation with a population of 200,000 has laws which severely restrict travel onto or off the island. There is an absolute prohibition against marrying foreigners, but island natives may marry as they wish. A non-lethal recessive genetic condition affects 2,000 of the people. How many carriers of this condition live on the island?
I. 198,000
II. 96,000
III. 36,000
IV. 12,400
V. 9,600
II
IV
I
III
V
III
The question assumes unusual conditions that must be met for a Hardy-Weinberg genetic equilibrium to exist. The population is large and isolated. The gene is assumed to be stable. Mating is "random," but only within the population. Here, the affected homozygous recessive people number 2,000—one one hundredth of the population.
In Hardy-Weinberg terms, this means q squared is 0.01 and q (the frequency of the recessive allele) is 0.1. Since p + q = 1, then p, the frequency of the dominant allele, must be 0.9. The carriers are denoted by 2pq because p + q = 1, and therefore p2 + 2pq + q2 is also equal to one. Here, 2 (0.9)(0.1) = 0.18, meaning that 18% of the 200,000 population, or 36,000 persons, are heterozygous carriers. The strict conditions for Hardy-Weinberg equilibrium are almost never satisfied in human populations.
Example Question #1163 : Mcat Biological Sciences
A botanist is reviewing a set of sequenced genomes from the tobacco plants he uses in his lab. He notices frequency of plants that are phenotypically recessive is 0.16. What are the frequencies of heterozygotes and homozygous dominant plants?
Heterozygotes = 0.60
Homozygous dominant = 0.40
Heterozygotes = 0.36
Homozygous dominant = 0.48
Heterozygotes = 0.40
Homozygous dominant = 0.60
Heterozygotes = 0.68
Homozygous dominant = 0.16
Heterozygotes = 0.48
Homozygous dominant = 0.36
Heterozygotes = 0.48
Homozygous dominant = 0.36
We use the formula:
where p and q are the allelic frequencies. We know that is the frequency of homozygous recessive individuals, so q must be 0.4 That means that p must be 0.6, because p and q must add up to 1. From there, we can just plug in 0.4 a 0.6 to get our answer.
Example Question #1164 : Mcat Biological Sciences
The concept of genomic imprinting is important in human genetics. In genomic imprinting, a certain region of DNA is only expressed by one of the two chromosomes that make up a typical homologous pair. In healthy individuals, genomic imprinting results in the silencing of genes in a certain section of the maternal chromosome 15. The DNA in this part of the chromosome is "turned off" by the addition of methyl groups to the DNA molecule. Healthy people will thus only have expression of this section of chromosome 15 from paternally-derived DNA.
The two classic human diseases that illustrate defects in genomic imprinting are Prader-Willi and Angelman Syndromes. In Prader-Willi Syndrome, the section of paternal chromosome 15 that is usually expressed is disrupted, such as by a chromosomal deletion. In Angelman Syndrome, maternal genes in this section are deleted, while paternal genes are silenced. Prader-Willi Syndrome is thus closely linked to paternal inheritance, while Angelman Syndrome is linked to maternal inheritance.
Figure 1 shows the chromosome 15 homologous pair for a child with Prader-Willi Syndrome. The parental chromosomes are also shown. The genes on the mother’s chromosomes are silenced normally, as represented by the black boxes. At once, there is also a chromosomal deletion on one of the paternal chromosomes. The result is that the child does not have any genes expressed that are normally found on that region of this chromosome.
A scientist discovers another genetic disease that has similar symptoms to Prader-Willi Syndrome. He discovers that this disease is recessive, and caused not by changes to chromosome 15, but by a point mutation on chromosome 3. He calculates the recessive allele frequency in a population to be .
Assuming the that normal allele, , and recessive allele, , are the only two alleles in this population, what is the percentage of the population that has the disease?
Based on Hardy-Weinberg principles, we can predict the phenotype and genotype frequencies of a given population based on the equation . In this equation, is the recessive allele frequency and is the recessive phenotype frequency, or frequency of homozygous recessive genotypes.
The genotype frequency of , necessary for the development of a recessive disease, is going to be the square of the recessive allele frequency, .
Example Question #21 : Population Genetics And Hardy Weinberg
A rare recessive mutation causes rabbits that are normally white to be pink. If one in a hundred rabbits is pink, what is the frequency of the pink allele?
We know that the pink allele is recessive and that one out of every hundred is pink; thus, one out of every hundred rabbits is homozygous recessive. Using Hardy-Weinberg calculations, we should be able to calculate the allele frequency.
If the pink allele frequency is , then is ; will refer to the frequency of homozygous recessive individuals in a population.
Using this set up, we can solve for the recessive allele frequency.
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