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EVOLUTIONARY BIOLOGY LABORATORY MANUAL

NAME: ________________________________________ SCORE: ____________


YEAR/COURSE/SECTION: ________________________ DATE: _____________

NATURAL SELECTION AND THE PRESERVATION OF GENETIC


DIVERSITY Activity No. 5

I. INTRODUCTION

Although the action of natural selection often results in a reduction of genetic


diversity, some forms of selection (collectively known as balancing selection) can maintain
genetic diversity. One form of balancing selection is heterozygote advantage, where the
heterozygote has a higher fitness than either homozygote. Heterozygote advantage is
sometimes called overdominance for fitness.

Perhaps the best-known case of heterozygote advantage is sickle cell anemia in


humans. Homozygotes for the sickle cell allele usually die before child-bearing years,
particularly in less-developed areas of the world. Despite the low fitness of the
homozygotes, the allele for sickle cell anemia can persist in malaria-infested regions of the
world because heterozygotes have increased resistance to malaria. Other likely examples
of heterozygote advantage include cystic fibrosis in humans, alleles at the Human
Leukocyte Antigen (HLA) system in humans, and resistance to the pesticide warfarin in
rats.

In this exercise, you will perform simulations that show the power of heterozygote
advantage.

II. SIMULATIONS

Go to cite: https://evolution4e.sinauer.com/simulations/05/natural_selection.html to
open the simulation window.

III. QUESTIONS

PROCUDURE 1: Set the population size to 100, with 25 AA, 50 Aa, and 25 aa individuals.

1. What is the initial frequency of the A allele?


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EVOLUTIONARY BIOLOGY LABORATORY MANUAL

2. Is the population at Hardy–Weinberg equilibrium (see textbook Chapter 4, pp. 83–85)?


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3. If the initial frequency of the A allele were 0.3 and the population size were 100, how
many individuals of each genotype would be in the population at Hardy–Weinberg
equilibrium?
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PROCEDURE 2: Set the fitnesses of all three genotypes (AA, Aa, aa) to 1.0. All genotypes
thus have equal fitnesses.

PROCEDURE 3: Run the simulation. Record if the A allele is fixed, lost, or remains
polymorphic throughout the 400 generations. If the A allele remains
polymorphic, record whether its frequency stayed between 0.25 and 0.75
(see lines of chart of frequency). Repeat for a total of 20 trials.

4. In how many trials did the A allele fix? In how many trials was it lost? In how many was it
polymorphic? In the cases where the A allele remains polymorphic after 400
generations, in how many trials did its frequency remain between 0.25 and 0.75
throughout the 400 generations?
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5. What evolutionary processes caused the changes in frequency of the A allele? What
evolutionary processes caused the loss and fixation of the A allele in those cases
where it was lost or fixed?
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PROCEDURE 4: Set the fitnesses of the genotypes so that the fitness of AA is 0.8, the
fitness of Aa is 1.0, and the fitness of aa is 0.8. This is a case of
heterozygote advantage.

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EVOLUTIONARY BIOLOGY LABORATORY MANUAL

PROCEDURE 5: Run the simulation. Record if the A allele is fixed, lost, or remains
polymorphic throughout the 400 generations. If the A allele remains
polymorphic, record whether its frequency stayed between 0.25 and 0.75
(see lines on chart of frequency). Repeat for a total of 10 trials.

6. In how many trials did the A allele fix? In how many trials was it lost? In how many was
it polymorphic? In the cases where the A allele remains polymorphic after 400
generations, in how many trials, did its frequency remain between 0.25 and 0.75
throughout the 400 generations?
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7. What evolutionary process is counteracted by balancing selection by heterozygote


advantage in the last simulations you performed?
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PROCEDURE 6: Set the initial frequency of the A allele to 0.8 by starting the population
with 128 AA, 64 Aa, and 8 aa individuals. Maintain the same values for
fitness: fitness of AA is 0.8, the fitness of Aa is 1.0, and the fitness of aa is
0.8. Run the simulation three times.

8. Describe what happens to the frequency of the A allele.


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IV. REFERENCES

Futuyma D. J. & Kirkpatrick M. (2017). Evolution, 4 th ed. Sunderland, Massachusetts:


Sinauer Associates, Inc.

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