## Instant Download with all chapters and Answers

Sample Chapters

***you will get test bank in PDF in best viewable format after buy***

Single-Gene Inheritance

MULTIPLE-CHOICE QUESTIONS

Sections 2.1. and 2.2. (Single gene inheritance, The chromosomal basis of single-gene

inheritance patterns)

1. If a plant of genotype A/a is selfed, and numerous offspring are scored, what proportion of the

progeny is expected to have homozygous genotypes?

A) 0

B) 25%

C) 50%

D) 75%

E) 100%

Answer: C

2. What is the maximum number of heterozygous genotypes that could be produced by

monohybrid self?

A) 1

B) 2

C) 3

D) 4

E) 6

Answer: A

3. A plant is heterozygous at three loci. How many different gamete genotypes can it theoretically

produce with respect to these three loci?

A) 2

B) 3

C) 4

D) 8

E) 16

Answer: D

4. In mountain rabbits, the EL-1 gene is located on chromosome 3. Four alleles of this gene have

been identified in the population. With respect to EL-1, what is the maximum number of

genotypes in the progeny of a single cross between two mountain rabbits?

A) 1

B) 2

C) 3

2

D) 4

E) 6

Answer: D

5. A wild-type strain of haploid yeast is crossed to a mutant strain with phenotype d. What

phenotypic ratios will be observed in the progeny?

A) all wild type

B) 75% wild type and 25% mutant (d)

C) 50% wild type and 50% mutant (d)

D) 25% wild type and 75% mutant (d)

E) all mutant (d)

Answer: C

Section 2.3. (The molecular basis of Mendelian inheritance patterns)

6. Mice (Mus musculus) have 40 chromosomes per diploid cell (2n = 40). How many double-

stranded DNA molecules and how many chromosomes are there in a mouse cell that is in the G2

stage of the cell cycle?

A) 40 DNA molecules and 20 chromosomes

B) 40 DNA molecules and 40 chromosomes

C) 40 DNA molecules and 80 chromosomes

D) 80 DNA molecules and 40 chromosomes

E) 80 DNA molecules and 80 chromosomes

Answer: D

7. A mutation occurs in a germ cell of a pure-breeding, wild-type male mouse prior to DNA

replication. The mutation is not corrected, and the cell undergoes DNA replication and a normal

meiosis producing four gametes. How many of these gametes will carry the mutation?

A) 1

B) 2

C) 3

D) 4

E) It is impossible to predict.

Answer: B

8. What is the mechanism that ensures Mendel’s first law of segregation?

A) formation of chiasmata

B) formation of the kinetochore

C) pairing of homologous chromosomes

D) segregation of homologous chromosomes during meiosis I

3

E) segregation of sister chromatids during meiosis II

Answer: D

9. A laboratory mouse homozygous for an RFLP marker is mated to a wild mouse that is

heterozygous for that marker. One of the heterozygous individuals resulting from this cross is

mated back to the wild parent. What proportion of the offspring will have the same RFLP pattern

as the original laboratory mouse?

A) none of the offspring

B) 1/4

C) 1/2

D) 3/4

E) all of the offspring

Answer: C

10. The diagram below shows a part of the biochemical pathway responsible for fruit color in

peppers (Caspicum annuum). Enzyme 1 is responsible for catalyzing the reaction that turns the

colorless precursor into yellow pigment, whereas Enzyme 2 catalyzes the step that turns the

yellow pigment into red pigment. A breeder crosses a pure-breeding plant that makes yellow

peppers to a pure-breeding plant that makes red peppers. What proportion of the offspring will

make red peppers?

Enzyme 1 Enzyme 2

Colorless precursor Yellow pigment Red pigment

A) all of the offspring

B) 3/4

C) 1/2

D) 1/4

E) none of the offspring

Answer: A

11. The wild-type eye color in the fruit fly Drosophila melanogaster is dark red, as a result of a

mixture of bright red and brown pigments. “Enzyme A” is encoded by the “a” gene, and is

required to synthesize the bright red pigment. A lack of red pigment results in a somewhat brown

eye color. You cross two fruit flies who are heterozygous for a recessive mutation that completely

inactivates the “a” gene. What proportion of their offspring will have a recessive eye color

phenotype?

A) all of the offspring

B) 3/4

C) 1/2

D) 1/4

E) none of the offspring

4

Answer: D

Section 2.4. (Some genes discovered by observing segregation ratios)

12. In pet rabbits, brown coat color is recessive to black coat color. A black female rabbit gives

birth to four black-coated and three brown-coated baby rabbits. What can be deduced about the

genotype of the baby rabbits’ father?

A) He could be heterozygous black/brown or homozygous brown.

B) He could be heterozygous black/brown or homozygous black.

C) He must be heterozygous black/brown.

D) He must be homozygous black.

E) He must be homozygous brown.

Answer: A

13. “Dumpy” is a commonly used mutant phenotype in the nematode worm C. elegans. Two

“Dumpy” individuals are crossed to each other, and this cross produces 210 “Dumpy” and 68

wild-type individuals. If one of the “Dumpy” individuals used in this cross was mated with a wild

type, what “Dumpy”: wild-type ratio would we observe in the offspring?

A) 0:1

B) 1:0

C) 1:1

D) 1:3

E) 3:1

Answer: C

14. A female rabbit of phenotype c′ is crossed to a male rabbit with c

ch. The F1 is comprised of

five rabbits with a c′ phenotype, two with c

ch phenotype, and three with c phenotype. Of the

phenotypically c rabbits, two are females and are backcrossed to their father. This cross produces

only rabbits with c

ch phenotype. These results suggest that:

A) c could be dominant or recessive to c′.

B) c is dominant to c′, but recessive to c

ch

.

C) c is dominant to c

ch, but recessive to c′.

D) c is dominant to both c′ and c

ch

.

E) c is recessive to both c′ and c

ch

.

Answer: E

15. A plant with small red flowers is crossed to a plant with large white flowers. The resulting F1

is comprised of 75 plants with small red flowers and 72 plants with small white flowers.

If flower color and flower size are controlled by a single gene each, what can be concluded from

these results?

A) Flower color is controlled by a sex-linked gene.

5

B) Red color and small size are dominant to white color and large size, respectively.

C) Small size is dominant to large size, but we can’t determine which color is dominant.

D) We can’t determine which color and which size are dominant.

E) White color and small size are dominant to red color and large size.

Answer: C

16. A dominant gene b

+

is responsible for the wild-type body color of Drosophila; its recessive

allele b produces black body color. A testcross of a heterozygous b

+

/b female by a black b/b

male gave 52 black and 58 wild-type progeny. If a black female from these progeny were crossed

with a wild-type brother, what phenotypic ratios would be expected in their offspring?

A) All males will be wild type, and all females will be black.

B) All progeny will be black.

C) All progeny will be wild type.

D) 75% will be wild type, 25% will be black.

E) 50% will be wild type, 50% will be black.

Answer: E

Section 2.5. (Sex-linked single-gene inheritance patterns)

17. A very common type of red–green colorblindness in humans is caused by a mutation in a

gene located on the X chromosome. Knowing that the mutant allele is recessive to the wild type,

what is the probability that the son of a woman whose father is colorblind is going to also be

colorblind?

A) 0%

B) 25%

C) 50%

D) 75%

E) 100%

Answer: C

18. A phenotypically normal woman is heterozygous for the recessive Mendelian allele causing

phenylketonuria, a disease caused by the inability to process phenylalanine in food. She is also

heterozygous for a recessive X-linked allele causing red–green colorblindness. What percentage

of her eggs will carry the dominant allele that allows normal processing of phenylalanine and the

X-linked recessive allele that causes colorblindness?

A) 0%

B) 25%

C) 50%

D) 75%

E) 100%

Answer: B

6

19. A rare, curly winged mutant of Drosophila was found in nature. A mating of this fly with a

true-breeding, normal laboratory stock produced progeny in the ratio 1 curly winged to 1 normal

(both sexes had the same ratio). All curly winged progeny of this cross, mated with normal

progeny of the same cross, again yielded 1 curly winged to 1 normal fly. When mated with one

another, the curly winged progeny of the first cross yielded a progeny of 623 curly : 323 normal.

This ratio strongly suggests which of the following?

A) Curly and normal are in the 3:1 ratio expected from intercrossing monohybrid genotypes for a

recessive mutant allele (curly).

B) Curly and normal are in the 3:1 ratio expected from intercrossing monohybrid genotypes for a

dominant mutant allele (curly).

C) The curly winged parent of the curly curly cross is homozygous.

D) Flies homozygous for the curly allele are lethal and never survive.

E) The gene for curly is sex-linked.

Answer: D

20. A female Drosophila with the mutant phenotype a is crossed to a male who has the mutant

phenotype b. In the resulting F1 generation all females are wild-type and all males have the a

mutant phenotype. Based on these results, we can conclude that the mode of inheritance of the

phenotypes of interest is:

A) autosomal for a and X-linked for b.

B) dominant for a and recessive for b.

C) recessive for a and dominant for b.

D) recessive for both a and b.

E) X-linked for a and autosomal for b.

Answer: D

21. A recessive X-linked gene mutation is known to generate premature baldness in males but is

without effect in women. If a heterozygous female marries an affected male, what proportion of

all their children is expected to be prematurely bald?

A) 1/4

B) 1/8

C) 1/16

D) 1/32

E) 1/216

Answer: A

Section 2.6. (Human pedigree analysis)

7

22. You have three jars of gumballs. The first jar has 100 white gumballs and 25 green, the

second jar has 50 white and 150 blue, and the third jar contains 500 white and 10 red.

If you randomly draw one gumball from each jar, what is the probability for all white gumballs?

A) 0.196 or 19.6%

B) 0.109 or 10.9%

C) 0.056 or 5.6%

D) 0.567 or 56.7%

E) This is impossible (0% chance).

Answer: A

23. You have three jars of gumballs. The first jar has 100 white gumballs and 25 green, the

second jar has 50 white and 150 blue, and the third jar contains 500 white and 10 red.

If you randomly draw one gumball from each jar, what is the probability for all white OR all

colored gumballs?

A) 0.199 or 19.9%

B) 0.112 or 11.2%

C) 0.058 or 5.8%

D) 0.589 or 58.9%

E) This is impossible (0% chance).

Answer: A

24. You have three jars of gumballs. The first jar has 100 white gumballs and 25 green, the

second jar has 50 white and 150 blue, and the third jar contains 500 white and 10 red.

If you randomly draw one gumball from each jar, what is the probability for at least one white

gumball?

A) 0.997 or 99.7%

B) 0.85 or 85%

C) 0.69 or 69 %

D) 0.034 or 3.4%

E) This is impossible (0% chance).

Answer: A

25. The following pedigree concerns the autosomal recessive disease phenylketonuria (PKU).

The couple marked A and B are contemplating having a baby but are concerned about the baby

8

having PKU. What is the probability of the first child having PKU? Unless you have evidence to

the contrary, assume that a person marrying into the pedigree (i.e., not a descendant of the two

parents at the top of the pedigree) is not a carrier. The filled-in individuals have PKU.

A) 0

B) 1/12

C) 1/4

D) 3/4

E) 9/64

Answer: B

26. The following pedigree depicts the inheritance of a rare hereditary disease affecting muscles.

What is the most likely mode of inheritance of this disease?

A) autosomal dominant

B) autosomal recessive

C) X-linked dominant

D) X-linked recessive

E) Y-linked

Answer: D

27. The following pedigree shows the inheritance of attached earlobes (black symbols) and

unattached earlobes (white symbol). Both alternative phenotypes are quite common in human

populations.

9

If the phenotypes are determined by alleles of one gene, then attached earlobes are inherited as:

A) an autosomal dominant trait.

B) an autosomal recessive trait.

C) a dominant trait that could be either autosomal or X-linked.

D) a recessive trait that could be either autosomal or X-linked.

E) an X-linked dominant trait.

Answer: A

28. In the human pedigree shown below, black symbols indicate individuals suffering from a rare

genetic disease, whereas white symbols represent people who do not have the disease.

Based on the pedigree, what is the most likely mode of inheritance of this rare genetic disease?

A) autosomal dominant

B) autosomal recessive

C) X-linked dominant

D) X-linked recessive

E) Y-linked

Answer: C

29. The following pedigree shows the inheritance of a mild, but very rare condition in Siberian

Husky dogs. If individuals 1 and 2 are crossed, what is the probability that they will produce an

affected pup?

A) 1/36

B) 1/16

C) 4/36

D) 4/16

E) 16/36

Answer: C

10

30. What is the probability that individual A is a heterozygous with respect to the condition

depicted in the pedigree?

A) 0%

B) 25%

C) 50%

D) 75%

E) 100%

Answer: E

31. What is the most likely mode of inheritance of the exceptionally rare condition represented in

the pedigree below, and why?

A) impossible to determine, because the condition is so rare

B) recessive, because it is only present in one generation, but we do not have enough

information to tell whether it’s X-linked or autosomal

C) recessive, because unaffected parents have an unaffected child, and autosomal, because there

are more autosomes than there are X chromosomes

D) X-linked recessive, because this would require the smallest number of rare alleles in the

pedigree

E) X-linked recessive, because it only affects a male, and his parents are unaffected

Answer: D

32. A couple is both heterozygous for the autosomal recessive disease cystic fibrosis (CF). What

is the probability that their first child will either be a boy or have CF?

A) 6/8

B) 5/8

C) 3/8

D) 2/8

E) 1/8

11

Answer: B

33. Cystic fibrosis is an autosomal recessive condition. If the parents of a boy with cystic fibrosis

have two more children, what is the probability that both of these children will be unaffected?

A) 1/16

B) 3/16

C) 4/16

D) 9/16

E) 16/16

Answer: D

MATCHING QUESTIONS

34. Below are a list of crosses and a list of progeny phenotypic ratios. Match each cross with the

expected progeny phenotypic ratio. Write the letter corresponding to the progeny phenotypic

ratio in the space provided on the right of each cross. Each progeny ratio may be used

multiple times. If a cross has no corresponding progeny ratio, write an “X” in the space

provided.

List of crosses

1) monohybrid self (diploids) _d__

2) monohybrid testcross (diploids) –a––

3) mutant wild-type in a haploid –a––

4) homozygous dominant homozygous recessive (diploid) –e––

5) mutant 1 mutant 2 in a haploid –a––

List of phenotypic ratios observed in the progeny

a) 1:1

b) 1:2:1

c) 2:1:1

d) 3:1

e) 1:0

35. Four patterns of inheritance and four pedigrees are shown below. Assume that individuals

marrying into the family are homozygous for the wild-type allele. Match each of the

inheritance patterns with a pedigree. If there is no pedigree to match an inheritance pattern,

write “X” beside that inheritance pattern.

A) autosomal dominant ______III____

B) autosomal recessive ______II____

C) X-linked dominant _______X___

D) X-linked recessive ______IV____

E) Y-linked _______I___

12

OPEN-ENDED QUESTIONS

Sections 2.1 and 2.2 (Single gene inheritance, The chromosomal basis of single-gene

inheritance patterns)

36. Mendel studied the inheritance of phenotypic characters determined by alleles of seven

different genes. It is an interesting coincidence that the pea plant has seven pairs of

chromosomes (n = 7). What is the probability that, by chance, Mendel’s seven genes would

each be located on a different chromosome? You may assume that the pea’s chromosomes

are all the same size.

Answer: 6!/76

= 6.12 * 103

Take each gene in turn. The probability is 1 that the first gene falls on a chromosome. The

probability that the second gene falls on any of the remaining six chromosomes is 6/7, the

next is 5/7, etc. The overall probability is the product of all these.

37. In Labrador retrievers, black color coat (B/–) is dominant to brown color coat (b/b). A

breeder crosses two black individuals who have previously produced some brown puppies. If

the cross produces six puppies:

a) what is the probability that the first born will be brown?

b) what is the probability that four of them will be brown and two will be black?

c) what is the probability that at least one of them will be brown?

Answer: a) Both parents must be heterozygotes B/b because they have previously produced

brown puppies. The probability that they produce a brown puppy is therefore 1⁄4.

b) Each pup has 3⁄4 chance of being black and 1⁄4 chance of being brown. The order in which

the brown and black puppies are born does not matter, so there are 15 different permutations

of 4 brown + 2 black (5!). Hence, the probability is:

15[(1/4)(1/4)(1/4)(1/4)(3/4)(3/4)] = 135/4096 = 3.3%

c) In this case, the only instance that does not satisfy the condition is the case in which all

puppies are black. The probability of this event is (3/4)6 = 729/4096 = 17.8%. Therefore, the

probability of obtaining at least one brown puppy is 1 (729/4096) = 82.2%.

13

38. In a particular species of plants, flower color is dimorphic: some individuals have red

flowers, whereas others have yellow flowers. If flower color is controlled by a single gene

with two alleles (c

red and c

yellow):

a) what would be the simplest way to determine which allele is dominant?

b) what will be the genotypic ratio in the offspring of a cross between a monohybrid and a

pure-breeding individual?

Answer: a) Crossing a pure-breeding red to a pure-breeding yellow individual, and assessing the

phenotype of the monohybrid produced. If it makes red flowers, then c

red is dominant; if it

makes yellow flowers, then c

yellow is dominant.

b) 1:1; half of the offspring will be heterozygous, and half will be homozygous like the pure-

breeding parent.

39. Suppose that red flower color (RR or Rr) is dominant to white flower color (rr) in a petunia.

A friend has a petunia plant with red flowers and wants to determine whether the plant is RR

or Rr.

a) What cross could you perform to help your friend determine the genotype of his petunia

plant?

b) How will this cross help you determine the genotype of your friend’s red-flowered

petunia? That is, how will the results from this cross differ if the red-flowered petunia is RR

versus Rr?

Answer: a) Perform a testcross (test the red petunia to a genotypically rr petunia).

b) You will observe different segregation in the testcross progeny, depending on the

genotype of the red petunia. If the red petunia is RR, then all testcross progeny will be red; if

the red petunia is Rr, then 1⁄2 of the testcross progeny will be red (Rr) and 1⁄2 will be white

(rr).

40. Suppose that a single gene controls fruit color in mango. Yellow fruit (Y) is dominant to red

fruit (y). Suppose a true-breeding yellow mango plant was crossed with a red-fruited plant,

and the resulting F1 was selfed. The F2 segregated as expected. If one of the yellow-fruited

plants was randomly selected and selfed, what is the probability that its progeny would

segregate for fruit color? Explain your logic.

Answer: The F2 consists of 1⁄4 YY: 1⁄2 Yy : 1⁄4 yy. Thus, the yellow-fruited plant that was randomly

picked could be either YY or Yy. There is a 1/3 chance that it was YY and 2/3 chance that it

was Yy. If a YY plant was selected and selfed, the progeny would not segregate for fruit

color. If a Yy plant was selected, the progeny would segregate for fruit color.

Section 2.3. (The molecular basis of Mendelian inheritance patterns)

14

41. The wild-type flower color of a particular species of plant is blue. The diagram below shows

a simplified version of the biochemical pathways responsible for the synthesis of the blue

pigment. Suppose that gene “A” codes for Enzyme A and gene “B” for Enzyme B.

A friend provides you with a pure-breeding plant that makes colorless (white) flowers. What

genetic experiment(s) could you perform to determine whether your plant lacks Enzyme A or

Enzyme B? (Suppose that you have access to any pure-breeding lines that you need.)

Enzyme A Enzyme B

Colorless precursor 1 Colorless precursor 2 Blue pigment

Answer: The “unknown” white mutant can be crossed to a pure-breeding mutant that lacks

Enzyme 2 (genotype b/b); if the “unknown” mutant lacks Enzyme 2, then the entire F1

should make only white (colorless) flowers, but if the “unknown” mutant lacks Enzyme 1,

then the F1 should inherit a functioning A allele from the b/b parent and a functioning B allele

from the “unknown” (a/a) parent, and therefore make blue flowers.

ALTERNATIVELY: A heterozygous A/a can be produced by crossing a wild type to a pure

line that lacks Enzyme A. This heterozygous can be crossed to the “unknown” mutant; if a

1:1 of blue:white is observed in the offspring, then our “unknown” mutant most likely lacks

Enzyme A and is therefore a/a.

42. Yellow leaves on a plant can be caused by genetic mutations, viruses, or unfavorable

environmental conditions. Suppose you find a plant that has yellow leaves, and you want to

determine if the cause of the phenotype is a genetic mutation or an environmental stress.

Design an experiment to differentiate between the different possibilities.

Answer: Cross the yellow plant with a normal plant. Self the resulting F1 and look for a

consistent, predictable segregation pattern. For example, the presence of a 3 green :1 yellow

segregation ratio would suggest that the yellow phenotype was caused by a recessive

mutation.

Section 2.4. (Some genes discovered by observing segregation ratios)

43. Suppose that the length of a duck’s tail is determined by a single autosomal gene with two

alleles: L (long tail) and l (short tail). When a female duck with a long tail was backcrossed

to her father, she produced three ducklings with a long tail and three with a short tail.

a) What are the possible genotypes of the female duck and of her father?

b) What is the most likely genotype of the female duck’s father? (Justify your answer using

probabilities).

Answer: a) The presence of ducklings with the recessive phenotype among the offspring indicates

that both the mother (the “female duck”) and the male used in the cross carry the recessive l

allele. The mother must be L/l as she has a long tail phenotype. The father could be L/l or l/l.

15

b) l/l is more likely. The probability of the cross L/l l/l producing a 1:1 ratio within an

offspring of six ducklings is [(1/2)6

]*10 = ~15%, whereas the probability that the cross L/l

L/l produce a 1:1 ratio in an offspring of six ducklings is [(3/4)3

(1/4)3

]*10 = ~6.6%.

44. Loppins are fictitious (but useful) diploid invertebrates that produce large offspring and

normally have long antennae. Short antennae mutants also exist. Unfortunately for the

geneticists working on these organisms, the males’ antennae don’t fully develop until the

loppin equivalence of “middle age.” A female with short antennae is crossed to a young male,

and all the females in their offspring have the short antennae mutant phenotype. A subset of

these F1 females are crossed to a middle-aged male with short antennae, and all the females

produced by these crosses have short antennae. However, all the crosses between the F1

females and their brothers produce both short antennae and long antennae loppins in a ratio of

about 3:1. How can these results be explained? Provide the genotypes of as many individuals

as possible.

Answer: The 3:1 ratio obtained in the cross between brothers and sisters suggests that short

antennae (S) is dominant to long antennae (s), and that the F1 females and their brothers are

heterozygous (S/s). The young male used in the original cross is probably homozygous for the

long antennae allele (s/s); the middle aged male with short antennae is probably homozygous

(S/S, because all the progenies have short antennae). The cross between F1 females and the

middle aged male produces about 50% S/s and 50% S/S individuals; the cross between the F1

females and their brothers produces about 25% S/S, 25% s/s and 50% S/s, hence the observed

phenotypic ratios.

Section 2.5. (Sex-linked single-gene inheritance patterns)

45. Wild-type Drosophila melanogaster have a brown/grey body color. Mutants exist that have

a yellow body color. Several crosses were performed between phenotypically wild type and

yellow individuals, and the results of each cross are reported in the table below.

Deduce the mode of inheritance of the yellow body phenotype and genotypes of the parents

and offspring in the following crosses.

Progeny

–––––––––––––––––––––––––––––––––––––

Females Males

Parents wild type yellow wild type yellow

Female Male –––––––––––––––––––––––––––––––––––––

a) wild type * yellow 198 0 203 0

b) yellow * yellow 0 156 0 145

c) yellow * wild type 210 0 0 190

d) wild type * yellow 102 98 99 97

Answer: All the offspring in cross (a) are wild type; yellow is recessive to wild type;

16

let’s define A as the dominant wild-type allele and a as the yellow mutant recessive. In all

the progenies we have roughly equal numbers of males and females, which is what is

expected. However, there is some sex bias and reciprocal crosses give different results: all

the sons of yellow females (homozygous a/a) are yellow; all the daughters of wild-type

males are wild type; this suggests sex-linkage.

In fact:

Progeny

–––––––––––––––––––––––––––––––––––––

Females Males

Parents wild type yellow wild type yellow

Female Male –––––––––––––––––––––––––––––––––––––

a) XA

/XA

* X

a

/Y X

A

/Xa X

a

/Xa X

A

/Y not possible

expected ratio all WT, as observed all WT, as observed

b) Xa

/Xa

* X

a

/Y not possible X

a

/Xa

not possible X

a

/Y

expected ratio all yellow, as observed all yellow, as observed

c) Xa

/Xa

* X

A

/Y X

A

/Xa

not possible not possible X

a

/Y

expected ratio all WT, as observed all yellow, as observed

d) XA

/Xa

* X

a

/Y X

A

/Xa X

a

/Xa X

A

/Y X

a

/Y

expected ratio 1:1, as observed 1:1, as observed

46. The black and yellow pigments in the coats of cats are controlled by an X-linked pair of

alleles. Females heterozygous for these alleles have areas of black and areas of yellow in

their coat (called tortoise-shell, or calico if there are also patches of white hair).

a) A calico cat has a litter of eight kittens: one yellow male, two black males, two yellow

females, and three calico females. Assuming there is a single father for the litter, what is his

probable color?

b) A yellow cat has a litter of four kittens: one yellow and three calico. Assuming there is a

single father for the litter, what is the probable sex of the yellow kitten?

c) How would you prove that XO cats are phenotypically female? What female kitten colors

(with respect to yellow, calico, and black) would you look for in which types of parental

color crosses?

Answer: a) Yellow (genotype: yw;Y chromosome) where yw = yellow; yw

+

= black

b) Male. Since the father must be black (genotype yw

+

;Y chromosome), the only true yellow

progeny cannot have received a color gene from the father. It must be male, and must have

received its one X chromosome from its mother.

c) Look for female kittens that fail to express an allele they should have inherited from their

mothers: black female kittens from yellow mothers or yellow female kittens from black

mothers. These kittens should have an X chromosome from their fathers as usual; the fact

that they show no alleles from their mothers may suggest they developed from eggs without

an X chromosome and therefore that XO is female. Similarly, look for female kittens that

fail to express a color that should have been inherited from their father. Female progeny of

yellow tom cats should be either yellow or calico and of black tom cats, either black or

17

calico, depending on the allele inherited from the mother. A black daughter of a yellow tom

cat might come from a sperm lacking any sex chromosome. Chromosomal checks would be

required on these unexpected progeny.

47. A young woman is worried about having a child because her mother’s only sister had a son

with Duchenne muscular dystrophy (DMD). The young woman has no brothers or sisters.

(DMD is a rare X-linked recessive disorder.)

a) Draw the relevant parts of the pedigree of the family described above. (Be sure to include

the grandmother, the three women mentioned, and all their mates.)

b) State the most likely genotype of everyone in the pedigree.

c) Calculate the probability that the young woman’s first child will have DMD.

Answer: a) pedigree and b) genotypes

c) The grandmother must have been D/d. There is a 1/2 chance that the mother is D/d and, if

so, a further 1/2 chance that the woman herself is D/d. If she is, 1/2 of her sons will have

DMD. Since the probability of a son is also 1/2, the overall probability is 1/2 * 1/2 * 1/2 *

1/2 = 1/16.

Section 2.6. (Human pedigree analysis)

48. a) In families with four children, what proportion of the families will have at least one boy?

b) In families with two girls and one boy, what fraction of the families will have the boy as

the second child?

c) In families with four children, what fraction of the families will have the gender order

male-female-female-male?

Answer: a) 0.9375, since 1 Prob. of 4 girls, or 1 (.5)4

= 1 0.0625. The frequency can be

calculated more laboriously by expanding the binomial (p + q)

4

= p

4

+ 4p

3

q + 6p

2

q

2

+ 4pq

3

+

q

4

and calculating that 15/16 (0.9375) of the distribution has one boy.

b) 1/3, because the frequencies of MFF, FMF, and FFM families are equal.

c) Of four-child families, 6/16 have two boys and two girls; only 1/6 of such families will

have the birth order MFFM. Therefore, 1/16 will have that particular birth order. The same

answer can be derived as (0.5)4

.

18

49. A man whose mother had cystic fibrosis (autosomal recessive) marries a phenotypically

normal woman from outside the family, and the couple considers having a child.

a) If the frequency of cystic fibrosis heterozygotes (carriers) in the general population is 1

in 25, what is the chance that the first child will have cystic fibrosis?

b) If the first child does have cystic fibrosis, what is the probability that the second child

will be normal?

Answer: a) The man must be a heterozygote, C/c. The probability that his wife is C/c is 1/25, and

if they are both C/c the probability of having an affected child is 1/4. Overall, the

probability is (1/25)(1/4) = 1/100.

b) The first child shows that both parents must have been C/c, so the probability that the

next child will be normal is 3/4.

50. Consider the following pedigree of a rare autosomal recessive disease. Assume all people

marrying into the pedigree do not carry the abnormal allele.

a) If individuals A and B have a child, what is the probability that the child will have the

disease?

b) If individuals C and D have a child, what is the probability that the child will have the

disease?

c) If the first child of C * D is normal, what is the probability that their second child will

have the disease?

d) If the first child of C * D has the disease, what is the probability that their second child

will have the disease?

Answer: a) Choosing M for unaffected and m for the disorder, male B must be M/m, and female

A has a 2/3 chance of being M/m. The overall chance of an affected child is 1 * 2/3 * 1/4 =

1/6.

b) If C’s mother A is heterozygous, C stands a 1/2 chance of being heterozygous. D’s

mother must be heterozygous, and D stands a 1/2 chance of inheriting that heterozygosity.

The overall chance of an affected child is 2/3 * 1/2 * 1 * 1/2 * 1/4 = 1/24.

c) The probability is still 1/24.

d) Now that we know individuals C and D must both be M/m, the chance of the second child

being m/m is 1/4.

19

51. Below is the pedigree of a family where some individuals are affected with a mild condition

of the skin.

a) Based on the pedigree, what is the most likely mode of inheritance of this condition, and

why?

b) Indicate the respective genotypes of each individual represented. For individuals who

could have two or more genotypes, calculate the relative probability of each possible

genotype.

c) What is the probability that individuals 1 and 2 will have an affected daughter?

Answer: a) Autosomal recessive; it is the only mode of inheritance whereby two unaffected

parents can have an affected daughter (as is the case for I-1 and I-2 and their first child).

b) A = WT; a = mild condition

The affected individuals are a/a; all four individuals in generation I are A/a; the unaffected

people in generation II have a probability of 2/3 of being A/a and 1/3 of being A/A; and

for individual “2” a few more calculations are required:

– if both her parents are A/A (probability of 1/9), then she’s A/A;

– if one of her parents is A/A and the other A/a (probability of 4/9), then she has a 50%

chance of being A/A and 50% chance of being A/a;

– if both of her parents are carriers (probability of 4/9), then she has a 2/3 chance of

being A/a and 1/3 chance of being A/A.

– Overall, her probability of being A/A is (1/9) + (1/2)(4/9) + (4/9)(1/3) = 13/27

and her probability of being A/a is (1/2)(4/9) + (4/9)(2/3) = 14/27

c) (14/27)(1/2) = 7/27

52. In the late 1800s, Mendel defined two fundamental laws of transmission genetics; these were

subsequently used to establish chromosome theory as scientists examined visible chromosomes

in meiotic cells. Define these two laws, and diagram where in the process of meiosis these two

processes actually occur.

Answer: Students can diagram meiosis, which is a healthy review of their understanding of the

process, and identify within this process the observations of Mendel (working without knowledge

of meiosis). Mendel’s first law focused upon the segregation of genetic determinants during

meiosis. This is essentially the anaphase I-mediated process of reducing ploidy during meiosis I.

Mendel’s second law, independent assortment, occurs during meiosis I as homologous

chromosomes are lined up and assorted to meiocytes. This process is distinctly random in each

meiotic process and is key to genetic diversity within gamete production.