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In a population of cattle, the following color distribution was noted: \(36 \%\) red \((R R), 48 \%\) roan \((R r),\) and \(16 \%\) white \((r r) .\) Is this population in a Hardy-Weinberg equilibrium? What will be the distribution of genotypes in the next generation if the Hardy-Weinberg assumptions are met?

Short Answer

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Answer: In the next generation, the distribution of genotypes will be 36% red (RR), 48% roan (Rr), and 16% white (rr) if the Hardy-Weinberg assumptions are met.

Step by step solution

01

Calculating allele frequencies

To find the allele frequencies, we can use the information given about the genotypes frequencies. Since RR (red) has a frequency of 36% and Rr (roan) has a frequency of 48%, we can calculate the frequency of the R allele (p) as follows: \(p = \frac{2 * RR~frequency + Rr~frequency}{2 * Total~frequency} = \frac{2 * 0.36 + 0.48}{2} = 0.6\) Now, to find the frequency of the r allele (q), we can use the fact that the sum of p and q must equal 1: \(q = 1 - p = 1 - 0.6 = 0.4\)
02

Testing for Hardy-Weinberg equilibrium

Now that we have the allele frequencies, we can use the Hardy-Weinberg equation to test if the population is in equilibrium. The expected frequencies for the various genotypes under Hardy-Weinberg equilibrium would be as follows: Expected \(RR (red) = p^2 = (0.6)^2 = 0.36\) Expected \(Rr (roan) = 2pq = 2*0.6*0.4 = 0.48\) Expected \(rr (white) = q^2 = (0.4)^2 = 0.16\) These expected genotype frequencies match the given color distribution from the problem. Therefore, this population is in Hardy-Weinberg equilibrium.
03

Predicting the next generation's genotype frequencies

Since the population meets the assumptions of the Hardy-Weinberg equilibrium, we can expect it to remain in equilibrium in the next generation. This means that the genotype frequencies in the next generation will be the same as the current generation: Next generation \(RR (red) = 36\%\) Next generation \(Rr (roan) = 48\%\) Next generation \(rr (white) = 16\%\) So, the distribution of genotypes in the next generation will be \(36\%\) red (RR), \(48\%\) roan (Rr), and \(16\%\) white (rr) if the Hardy-Weinberg assumptions are met.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Allele Frequency
Allele frequency describes how common an allele is in a population. Alley frequency is crucial for studying Hardy-Weinberg Equilibrium. It allows us to determine the genetic composition and variability within a population.

To understand allele frequency better, imagine each organism as having two alleles for any gene. In a diploid organism, these alleles can be dominant or recessive. For our cattle exercise, we have alleles 'R' (for red) and 'r' (for white). Therefore, calculating the frequencies of each allele helps us predict the population's genetic structure.

The formula to calculate allele frequency is:
  • For allele 'R', the frequency (p) is determined by the equation:\[ p = \frac{2 \times \text{frequency of } RR + \text{frequency of } Rr}{2 \times \text{total frequency}} \]
  • For allele 'r', the frequency (q) can be simply obtained by subtracting 'p' from 1: \( q = 1 - p \)
Using these calculations, we find that in the cattle population, 'R' has a frequency of 0.6 and 'r' a frequency of 0.4. These are foundational for determining the genetic distribution under Hardy-Weinberg equilibrium.
Genotype Distribution
Genotype distribution is about understanding how different combinations of alleles are spread in a population. It helps to visualize how individual organisms express their genetic information.

In our cattle exercise, the genotypes are represented by combinations of 'R' and 'r' alleles: RR, Rr, and rr. The frequency of each genotype can be tested against Hardy-Weinberg Equilibrium expectations:
  • For homozygous dominant (RR), the expected frequency is \( p^2 \)
  • For heterozygous (Rr), it's \( 2pq \)
  • And for homozygous recessive (rr), it's \( q^2 \)
These calculations serve two purposes: confirm if the population is in equilibrium, and predict future distributions.
The observed genotype frequencies of 36% (RR), 48% (Rr), and 16% (rr) perfectly match the expected values. Hence, the population's distribution aligns with Hardy-Weinberg equilibrium.
Population Genetics
Population genetics is a critical field that examines genetic variations within populations and how these change over time and generations. It employs principles like Hardy-Weinberg Equilibrium to provide insights into evolutionary processes and genetic diversity.

In a stable population, modeled by Hardy-Weinberg, allele and genotype frequencies remain constant over generations—assuming no evolutionary forces are acting. This means random mating, no natural selection, no genetic drift, no migration, and no mutation.
Understanding this equilibrium is essential as it works as a null model in genetics. Deviation from this model allows scientists to detect evolutionary influences such as selection or genetic drift.

For the cattle population studied, the genetic equilibrium was confirmed since the observed and expected frequencies match. This consistency signals that, at least for the traits studied, no disruptive evolutionary forces appear to be at play. This allows the prediction that subsequent generations will maintain the same genetic structure, which is vital for breeding programs or conservation efforts.

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Most popular questions from this chapter

Consider a population in which the frequency of allele \(A\) is \(p=0.7\) and the frequency of allele \(a\) is \(q=0.3,\) and where the alleles are codominant. What will be the allele frequencies after one generation if the following occurs? (a) \(w_{A A}=1, w_{A a}=0.9, w_{a a}=0.8\) (b) \(w_{A A}=1, w_{A a}=0.95, w_{a a}=0.9\) (c) \(w_{A A}=1, w_{A a}=0.99, w_{a a}=0.98\) (d) \(w_{A A}=0.8, w_{A a}=1, w_{a a}=0.8\)

Achondroplasia is a dominant trait that causes a characteristic form of dwarfism. In a survey of 50,000 births, five infants with achondroplasia were identified. Three of the affected infants had affected parents, while two had normal parents. Calculate the mutation rate for achondroplasia and express the rate as the number of mutant genes per given number of gametes.

Population geneticists study changes in the nature and amount of genetic variation in populations, the distribution of different genotypes, and how forces such as selection and drift act on genetic variation to bring about evolutionary change in populations and the formation of new species. From the explanation given in the chapter, what answers would you propose to the following fundamental questions? (a) How do we know how much genetic variation is in a population? (b) How do geneticists detect the presence of genetic variation as different alleles in a population? (c) How do we know whether the genetic structure of a population is static or dynamic? (d) How do we know when populations have diverged to the point that they form two different species? (e) How do we know the age of the last common ancestor shared by two species?

Price et al. (1999. J. Bacteriol. 181: 2358-2362) conducted a genetic study of the toxin transport protein (PA) of Bacillus anthracis, the bacterium that causes anthrax in humans. Within the 2294 -nucleotide gene in 26 strains they identified five point mutations-two missense and three synonyms-among different isolates. Necropsy samples from an anthrax outbreak in 1979 revealed a novel missense mutation and five unique nucleotide changes among ten victims. The authors concluded that these data indicate little or no horizontal transfer between different \(B\). anthracis strains. (a) Which types of nucleotide changes (missense or synonyms) cause amino acid changes? (b) What is meant by horizontal transfer? (c) On what basis did the authors conclude that evidence of horizontal transfer is absent from their data?

A form of dwarfism known as Ellis-van Creveld syndrome was first discovered in the late 1930 s, when Richard Ellis and Simon van Creveld shared a train compartment on the way to a pediatrics meeting. In the course of conversation, they discovered that they each had a patient with this syndrome. They published a description of the syndrome in \(1940 .\) Affected individuals have a short-limbed form of dwarfism and often have defects of the lips and teeth, and polydactyly (extra fingers. The largest pedigree for the condition was reported in an Old Order Amish population in eastern Pennsylvania by Victor McKusick and his colleagues (1964). In that community, about 5 per 1000 births are affected, and in the population of \(8000,\) the observed frequency is 2 per \(1000 .\) All affected individuals have unaffected parents, and all affected cases can trace their ancestry to Samuel King and his wife, who arrived in the area in \(1774 .\) It is known that neither King nor his wife was affected with the disorder. There are no cases of the disorder in other Amish communities, such as those in Ohio or Indiana. (a) From the information provided, derive the most likely mode of inheritance of this disorder. Using the HardyWeinberg law, calculate the frequency of the mutant allele in the population and the frequency of heterozygotes, assuming Hardy-Weinberg conditions. (b) What is the most likely explanation for the high frequency of the disorder in the Pennsylvania Amish community and its absence in other Amish communities?

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