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In a population that meets the Hardy-Weinberg equilibrium assumptions, 81% of the individuals are homozygous for a recessive allele. What percentage of the individuals would be expected to be heterozygous for this locus in the next generation?

Short Answer

Expert verified
Answer: 18%

Step by step solution

01

Understand Hardy-Weinberg equilibrium equation

The Hardy-Weinberg equilibrium equation is given by the formula: p2+2pq+q2=1, where p is the frequency of the dominant allele, q is the frequency of the recessive allele, p2 represents the frequency of homozygous dominant individuals, 2pq represents the frequency of heterozygous individuals, and q2 represents the frequency of homozygous recessive individuals in a population.
02

Calculate frequency of homozygous recessive individuals

We are given that 81% of the population are homozygous recessive individuals. To get the frequency, we need to convert this percentage into a decimal. So, q2=0.81.
03

Calculate frequency of recessive allele

To find the frequency of the recessive allele (q), take the square root of the frequency of homozygous recessive individuals: q=q2=0.81=0.9.
04

Calculate frequency of dominant allele

Since there are only two types of alleles for a locus in the Hardy-Weinberg equilibrium, we can calculate the frequency of the dominant allele (p) using the formula: p=1q. So, p=10.9=0.1.
05

Calculate frequency of heterozygous individuals

Now, we can use the Hardy-Weinberg equilibrium equation to find the frequency of heterozygous individuals (2pq): 2pq=2×0.1×0.9=0.18.
06

Convert frequency into percentage

Finally, to express the frequency of heterozygous individuals as a percentage, multiply the frequency by 100: 0.18×100=18%. So, we would expect 18% of the individuals in the next generation to be heterozygous for this locus.

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Key Concepts

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

Homozygous Recessive Individuals
Homozygous recessive individuals are key to understanding genetic variations in a population. These are individuals who carry two copies of the same recessive allele for a specific gene. When considering the Hardy-Weinberg equilibrium, which serves as a model for genetic distribution in a population, homozygous recessive individuals are represented by the term q2 in the equation. This model assumes no evolution is occurring—that is, the frequencies of alleles (gene variants) do not change over time.

In practical terms, if 81% of a population are homozygous recessive, this tells us the frequency of this genetic trait within that group. It's quite straightforward to evaluate the presence of this trait in future generations by using the Hardy-Weinberg equation, which in turn helps predict genetic diversity and potential for genetic diseases linked to recessive alleles.
Allele Frequency
Allele frequency is the cornerstone of population genetics. It measures how common a particular allele—or version of a gene—is in a population. Two frequencies are at play: one for the dominant allele (represented by p) and one for the recessive allele (q). These frequencies are crucial because they determine the genetic variability and potential evolutionary changes in a group of organisms.

The Hardy-Weinberg equation, p2+2pq+q2=1, hinges on the fact that the sum of these probabilities (p and q) is 1, or 100 percent. When the allele frequencies are known, as in our exercise where q was calculated to be 0.9, scientists can gauge the genetic makeup of the next generation—helping to predict prevalence of diseases, response to selection pressures, or even how a population might adapt to environmental changes.
Heterozygous Individuals
Heterozygous individuals possess two different alleles for a given gene, one from each parent. In terms of the Hardy-Weinberg equilibrium, these individuals are significant because their genetic makeup includes both dominant and recessive alleles, represented by 2pq in the formula. This heterozygosity is essential for maintaining genetic diversity within a population, contributing to the ability of a species to adapt and survive in changing environments.

Knowing the percentage of heterozygous individuals, like the 18% calculated in the exercise, provides insight into the genetic structure of a population. This balance between homozygosity and heterozygosity shapes the overall genetic health and resilience against potential threats, such as diseases or changes in habitat.

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Most popular questions from this chapter

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?

The genetic difference between two Drosophila species, D. heteroneura and D. sylvestris, as measured by nucleotide diversity, is about 1.8 percent. The difference between chimpanzees (P. troglodytes) and humans (H. sapiens) is about the same, yet the latter species are classified in different genera. In your opinion, is this valid? Explain why.

The use of nucleotide sequence data to measure genetic variability is complicated by the fact that the genes of higher eukaryotes are complex in organization and contain 5 and 3 flanking regions as well as introns. Researchers have compared the nucleotide sequence of two cloned alleles of the γ -globin gene from a single individual and found a variation of 1 percent. Those differences include 13 substitutions of one nucleotide for another and 3 short DNA segments that have been inserted in one allele or deleted in the other. None of the changes takes place in the gene's exons (coding regions). Why do you think this is so, and should it change our concept of genetic variation?

Calculate the frequencies of the AA,Aa, and aa genotypes after one generation if the initial population consists of 0.2AA,0.6 Aa, and 0.2 aa genotypes and meets the requirements of the Hardy-Weinberg relationship. What genotype frequencies will occur after a second generation?

What is the original source of genetic variation in a population? Which natural factors affect changes in this original variation?

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