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Introduction
The Augustinian monk Gregor Mendel (1822-1884) conducted his experiments within the confines of a quiet
monastery garden in almost complete anonymity. His findings were written down, but only after his death were his
contributions to genetics recognized. Mendel chose the common garden pea, Pisum sativum, as his experimental
model. It was an excellent choice. The plants were commercially available, easy to cultivate and grew rapidly.
Different varieties had clearly different characteristics that “bred true”—reappearing consistently in crop after crop.
Also the sexual structures of the plant are completely enclosed within the petals of the flower; consequently the flower
normally self-pollinates (sperm from the flower’s own pollen fertilizes its egg cells) essentially creating genetic clones
of the parent. If pea flowers were pollinated by insects, the large number of hybrid offspring and the genetic variety
created would have clouded Mendel’s results and made the clear patterns that led to Mendel’s conclusions impossible
to detect.
Many other people may have noticed genetic effects just as Mendel did, but it was Mendel’s application of
mathematical interpretation to his results and his clear replicable reporting of the experiments that was revolutionary
for its time.
Mendel’s experiments
Mendel’s experiments were an extension of the efforts of a long line of biologists and farmers that studied the effects
of unifying (hybridizing) two different parental stocks. It had long been thought that heredity was purely a blending
process, with offspring being a “dilution” of different parental characteristics. It was Mendel who demonstrated the
appearance and disappearance of traits follows specific laws which could be determined merely by counting the
different characteristics of offspring produced from any particular set of crosses.
Mendel found seven traits that he could observe clearly being passed from parents to offspring: seed form and color,
flower position and color, pod form and color, and stem length (height of plant). Mendel began each experiment by
intentionally dusting the pollen from one parent onto the stigma of the flower of another variety. He called this first
cross the “parental generation”; abbreviated P. The first generation of offspring of the parents was called F1 (meaning
family number one). In every case Mendel found that the F 1 generation showed the same trait as only one of the
parents. This is called the dominant phenotype or trait. When the F1 offspring were allowed to self-fertilize
(essentially crossing two F1 organisms) Mendel observed a return of some of the missing traits, which he called the
recessive trait. The second generation is known as F 2.
Mendel formulated this idea following a second set of experiments where he studied the inheritance of two traits at
once (e.g. one parent plant had seeds that were round and yellow, and another parent had seeds that were wrinkled and
green.) As seen in Table 1, the round and yellow traits are dominant, and the wrinkled and green are recessive. As
you would expect, all seeds produced in the F1 generation showed the dominant phenotype. When the F1 seeds were
allowed to self-pollinate, 556 seeds were produced in the F 2 generation. The results are shown in Table 2 below.
Table 2: Results from the F2 generation following a cross of round yellow and wrinkled green parents
in the P generation.
Tally and compare separately the round vs. wrinkled ratio and the yellow vs. green ratio to see if the traits
follow a Mendelian 3:1 ratio.
# round # wrinkled Ratio (2 decimal places)
These experimental results did not contradict Mendel’s early experiments. Round and wrinkled still appeared in the
same 3:1 ratio and so did yellow and green. But the round and yellow traits and the wrinkled and green traits, which
had originally combined in one parent plant each, sorted themselves out as if they were independent of one another.
Calculate the phenotype ratio when taking both traits into account (hint: divide the number of each
observed phenotype by the number observed for the double-recessive trait).
: : : 1
Adapted from Ward’s Natural Science Establishment: Principle of Mendelian Genetics, 1995.
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Activity 1
In this activity you will see how the laws of chance relate to biological occurrences. Mendel realized the role
of chance in heredity and it was a radical concept for its time.
What are the odds of a normal coin landing heads up after being flipped?
What is the probability (odds) of two coins both landing heads up after being flipped? (Hint: the probability
of a sequential event is the probability of each event separately, multiplied together.)
What is the probability of three coins all landing heads up after being flipped?
Imagine three coins are flipped, but one at a time. The first two coins both land heads. What are the odds of
the last coin landing heads up?
Procedure
1. Complete the Punnett squares below. (A = any generic dominant trait; a = any generic recessive trait)
a) Aa x Aa cross b) Aa x aa cross
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2. Create a Punnett square to predict the outcome of tossing two coins (assume heads is one allele and tails
is the other, neither is dominant).
3. Flip or toss your two coins 100 times (Yes, you have to do it 100 times). Put tallies in the top boxes and
then count the tallies and write the number in the total row of the table.
Actual total
Predicted
3a. Fill in the predicted number (based out of 100 flips) of each category based on your Punnett square
from question #1.
Do the actual results match your prediction? Explain why they do or do not.
4. If you toss the coins 1000 times instead of 100, would you expect the actual and predicted numbers to
match more closely than you saw after 100 flips, be the same as after 100, or become very different?
Explain.
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Activity 2
This activity investigates crosses between pea plants that are different in two trait characteristics (a dihybrid cross)
with each pair having one dominant and one recessive allele—and how each gene pair acts independently of the other.
Phenotypes in the resultant generations will be, on average, in a ratio of 9:3:3:1, demonstrating the independence, or
independent assortment, of these two gene pairs.
Materials needed (per team of two students)
Two (2) four-sided pyramidal dice—each numbered point represents a possible gene pair that the parents could pass on.
1. Which traits (seed form and seed color) are dominant? _______________ _________________
2. What is the genotype of the F1 generation following Mendel’s P cross of a pure dominant pea plant
(RRYY) with a double recessive plant (rryy)? Hint: this is easy, think about what alleles each parent
will contribute and put them together in a new genotype
3. Complete the Punnett square showing possible outcomes for the F2 generation (cross RrYy x RrYy).
RRYY
rryy
4. Calculate the expected phenotypic ratio based on the outcome of the Punnett square.
: : : 1 green wrinkled
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5. Use the two four-sided dice to generate some random data that simulates the uniting of gene pairs in a
new organism (zygote). Read the dice by reading the number on the point of each die that is
facing up. The two numbers correspond to a pair of alleles as shown in the chart in the materials
section. Thus a roll of 1, 4 would represent RY and ry coming together as the genotype RrYy. The
phenotype for this combination is Round Yellow, so that is the column where the mark is written.
Toss the dice about 80 times and record the phenotypes generated by each roll in the chart below (use
a tally mark ‘ for each one). If you accidentally go over 80, use all data you have.
wrinkled
Round Yellow Round green wrinkled green
Yellow
1,1 1, 2 1,3 1,4 2,3 2,2 2,4 4,4
3,3 3,4
Totals
Use your totals and calculate the phenotypic ratio observed from the dice toss (use 2 decimal places).
: : :
6. Put your data on the board as directed by your teacher. Total all the class data and recalculate
the phenotypic ratio for the whole class total.
Explain (referencing rules of probability as related to sample size) any differences seen from group to
group and overall compared to the predicted outcome. In other words, why is the class total (or
maybe certain individual groups) closer to the “perfect” 9:3:3:1 ratio than others are?