Essentials Of Genetics 8th Edition by William S. Klug – Test Bank
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Essentials of Genetics, 8 (Klug)
Chapter 3 Mendelian Genetics
1) Name the single individual whose work in the mid-1800s
contributed to our understanding of the particulate nature of inheritance as
well as the basic genetic transmission patterns. With which organism did this
person work?
1. A)
Gregor Mendel; Pisum
sativum
2. B)
George Beadle; Neurospora
3. C)
Thomas Hunt Morgan; Drosophila
4. D)
Calvin Bridges; Drosophila
5. E) Boris
Ephrussi; Ephestia
Answer: A
Section: Introduction
2) A recessive allele in tigers causes the white tiger. If two
normally pigmented tigers are mated and produce a white offspring, what
percentage of their remaining offspring would be expected to have normal
pigmentation?
1. A)
25%
2. B)
50%
3. C)
about 66%
4. D)
75%
5. E)
about 90%
Answer: D
Section: 3.2
3) Polydactyly is expressed when an individual has extra fingers
and/or toes. Assume that a man with six fingers on each hand and six toes on each
foot marries a woman with a normal number of digits. Having extra digits is
caused by a dominant allele. The couple has a son with normal hands and feet,
but the couple’s second child has extra digits. What is the probability that
their next child will have polydactyly?
1. A)
1/32
2. B)
1/8
3. C)
7/16
4. D)
1/2
5. E)
3/4
Answer: D
Section: 3.2
4) Tightly curled or wooly hair is caused by a dominant gene in
humans. If a heterozygous curly-haired person marries a person with straight
hair, what percentage of their offspring would be expected to have straight
hair?
1. A)
25%straight
2. B)
50% straight
3. C)
75% straight
4. D)
100% straight
5. E) It
is impossible to predict the outcome.
Answer: B
Section: 3.2
5) Which types of phenotypic ratios are likely to occur in
crosses when dealing with a single gene pair for which all the genotypic
combinations are of equal viability?
1. A)
9:3:3:1, 27:9:9:9:3:3:3:1
2. B)
1:2:1, 3:1
3. C)
1:4:6:4:1, 1:1:1:1
4. D)
12:3:1, 9:7
5. E)
2:3, 1:2
Answer: B
Section: 3.2
6) Assume that a black guinea pig crossed with an albino guinea
pig produced 5 black offspring. When the albino was crossed with a second black
guinea pig, 4 black and 3 albino offspring were produced. What genetic
explanation would apply to these data?
1. A)
albino = recessive; black = recessive
2. B)
albino = dominant; black = incompletely dominant
3. C)
albino and black = codominant
4. D)
albino = recessive; black = dominant
5. E)
None of the answers listed are correct.
Answer: D
Section: 3.2
7) The fundamental Mendelian process that involves the
separation of contrasting genetic elements at the same locus is called
________.
1. A)
segregation.
2. B)
independent assortment
3. C)
continuous variation
4. D)
discontinuous variation
5. E)
dominance or recessiveness
Answer: A
Section: 3.2
8) Which of the following groups of scientists were influential
around the year 1900 in setting the stage for our present understanding of
transmission genetics?
1. A)
Beadle, Tatum, Lederberg
2. B)
Watson, Crick, Wilkins, Franklin
3. C)
deVries, Correns, Tschermak, Sutton, Boveri
4. D)
Darwin, Mendel, Lamarck
5. E)
Hippocrates, Aristotle, Kolreuter
Answer: C
Section: 3.5
9) The Chi-square test involves a statistical comparison between
measured (observed) and predicted (expected) values. One generally determines
degrees of freedom as ________.
1. A)
the number of categories being compared
2. B)
one less than the number of classes being compared
3. C)
one more than the number of classes being compared
4. D)
ten minus the sum of the two categories
5. E)
the sum of the two categories
Answer: B
Section: 3.8
10) According to Mendel’s model, because of ________, all
possible combinations of gametes will be formed in equal frequency.
Answer: independent assortment
Section: Introduction
11) Assume that in a series of experiments, plants with round
seeds were crossed with plants with wrinkled seeds and the following offspring
were obtained: 220 round and 180 wrinkled.
(a) What is the most probable genotype of each parent?
(b) What genotypic and phenotypic ratios are expected?
(c) Based on the information provided in part (b), what are the
expected (theoretical) numbers of progeny (400 total) of each phenotypic class?
Answer:
(a) assuming that round (W) is
dominant to wrinkled (w): Ww X ww
(b) 1:1
(c) 200
Section: 3.2
12) In peas, gray seed color is dominant to white. For the
purposes of this question, assume that Mendel crossed plants with gray seeds
with each other and the following progeny were produced: 320 gray and 80 white.
(a) What is the most probable genotype of each parent?
(b) What genotypic and phenotypic ratios are expected in the
progeny of such a cross?
Answer:
(a) assuming the following symbols: G = gray and g = white, Gg X Gg
(b) genotypic = 1:2:1, phenotypic = 3:1
Section: 3.2
13) Assume that you have a garden and some pea plants have solid
leaves and others have striped leaves. You conduct a series of crosses [(a)
through (e)] and obtain the results given in the table.
Cross Progeny
solid
striped
(a) solid X
striped
55
60
(b) solid X
solid
36
0
(c) striped X
striped
0
65
(d) solid X solid
92
30
(e) solid X
striped
44
0
Define gene symbols and give the possible genotypes of the
parents of each cross.
Answer:
(a) From cross (d), assume that solid (S) is dominant to
striped (s): Ss X ss.
(b) SS X SS or SS X Ss
(c) ss X ss
(d) Ss X Ss
(e) SS X ss
Section: 3.2
14) Albinism, lack of pigmentation in humans, results from an
autosomal recessive gene (a).
Two parents with normal pigmentation have an albino child.
(a) What is the probability that their next child will be
albino?
(b) What is the probability that their next child will be an
albino girl?
(c) What is the probability that their next three children will
be albino?
Answer:
(a) 1/4
(b) 1/4 X 1/2 = 1/8
(c) 1/4 X 1/4 X 1/4 = 1/64
Section: 3.2
15) Dentinogenesis
imperfecta is a rare, autosomal, dominantly inherited disease
of the teeth that occurs in about one in 8000 people (Witkop 1957). The teeth
are somewhat brown in color, and the crowns wear down rapidly. Assume that a
male with dentinogenesis
imperfecta and no family history of the disease marries a
woman with normal teeth. What is the probability that
(a) their first child will have dentinogenesis imperfecta?
(b) their first two children will have dentinogenesis imperfecta?
(c) their first child will be a girl with dentinogenesis imperfecta?
Answer:
(a) 1/2
(b) 1/2 X 1/2 = 1/4
(c) 1/2 X 1/2 = 1/4
Section: 3.2
16) A certain type of congenital deafness in humans is caused by
a rare autosomal (not X-linked) dominant gene.
(a) In a mating involving a deaf man and a deaf woman (both
heterozygous), would you expect all the children to be deaf? Explain your
answer.
(b) In a mating involving a deaf man and a deaf woman (both
heterozygous), could all the children have normal hearing? Explain your answer.
(c) Another form of deafness is caused by a rare autosomal
recessive gene. In a mating involving a deaf man and a deaf woman, could some
of the children have normal hearing? Explain your answer.
Answer:
(a) No. In a mating involving heterozygotes, three genotypic
classes are expected in the offspring: fully dominant, fully recessive, and
heterozygous.
(b) Assuming that the parents are heterozygotes (because the
gene is rare), it is possible that all of the children could have normal
hearing.
(c) Because the gene in question is recessive, both of the
parents are homozygous and one would not expect normal hearing in the
offspring.
Section: 3.2
17) Assuming no crossing over between the gene in question and
the centromere, when do alleles segregate during meiosis?
Answer: meiosis I, when homologous chromosomes go to
opposite poles
Section: 3.2
18) Assuming a typical monohybrid cross in which one allele is
completely dominant to the other, what ratio is expected if the F1s are
crossed?
Answer: 3:1
Section: 3.2
19) Albinism, lack of pigmentation in humans, results from an
autosomal recessive gene (a).
Two parents with normal pigmentation have an albino child. What is the
probability that their next child will be albino?
Answer: 1/4
Section: 3.2
20) Albinism, lack of pigmentation in humans, results from an
autosomal recessive gene (a).
Two parents with normal pigmentation have an albino child. What is the
probability that their next child will be an albino girl?
Answer: 1/4 X 1/2 = 1/8
Section: 3.2
21) Albinism, lack of pigmentation in humans, results from an
autosomal recessive gene (a).
Two parents with normal pigmentation have an albino child. What is the
probability that their next three children will be albino?
Answer: 1/4 X 1/4 X 1/4 = 1/64
Section: 3.2
22) The autosomal (not X-linked) gene for brachydactyly, short
fingers, is dominant to normal finger length. Assume that a female with
brachydactyly in the heterozygous condition is married to a man with normal
fingers. What is the probability that
(a) their first child will have brachydactyly?
(b) their first two children will have brachydactyly?
(c) their first child will be a brachydactylous girl?
Answer:
(a) 1/2
(b) 1/2 X 1/2 = 1/4
(c) 1/2 X 1/2 = 1/4
Section: 3.2
23) Tightly curled hair is caused by a dominant autosomal gene
in humans. If a heterozygous curly-haired person marries a person with straight
hair, what phenotypes (and in what proportions) are expected in the offspring?
Answer: 1/2 curly (because the curly-haired individual is
most likely heterozygous); 1/2 straight hair
Section: 3.2
24) A certain type of congenital deafness in humans is caused by
a rare autosomal dominant gene. In a mating involving a deaf man and a deaf
woman (both heterozygous), would you expect all the children to be deaf?
Explain your answer.
Answer: No. In a mating involving heterozygotes, three
genotypic classes are expected in the offspring: fully dominant, fully
recessive, and heterozygous.
Section: 3.2
25) A certain type of congenital deafness in humans is caused by
a rare autosomal dominant gene. In a mating involving a deaf man and a deaf
woman, could all the children have normal hearing? Explain your answer.
Answer: Assuming that the parents are heterozygotes
(because the gene is rare), it is possible that all of the children could have
normal hearing.
Section: 3.2
26) A certain type of congenital deafness in humans is caused by
a rare autosomal recessive gene. In a mating involving a deaf man and a deaf
woman, could some of the children have normal hearing? Explain your answer.
Answer: Because the gene in question is recessive, both of
the parents are homozygous and one would not expect normal hearing in the
offspring.
Section: 3.2
27) What are two typical testcross ratios?
Answer: 1:1 and 1:1:1:1
Section: 3.2
28) The phenotype of vestigial (short) wings (vg) in Drosophila melanogaster is
caused by a recessive mutant gene that independently assorts with a recessive
gene for hairy (h) body.
Assume that a cross is made between a fly with normal wings and a hairy body
and a fly with vestigial wings and normal body hair. The wild-type
F1 flies were crossed among each other to produce 1024 offspring. Which phenotypes
would you expect among the 1024 offspring, and how many of each phenotype would
you expect?
Answer: Phenotypes: wild, vestigial, hairy, vestigial
hairy
Numbers expected: wild (576), vestigial (192), hairy (192),
vestigial hairy (64)
Section: 3.3
29) Which phenotypic ratio is likely to occur in crosses of two
completely dominant, independently segregating gene pairs when both parents are
fully heterozygous?
Answer: 9:3:3:1
Section: 3.3
30) Provide simple definitions that distinguish segregation and
independent assortment.
Answer: Segregation is the separation of alleles during
meiosis; independent assortment states that a member of one gene pair has an
equal and independent opportunity of segregating with either member of another
gene pair.
Section: 3.3
31) Under what conditions does one expect a 9:3:3:1 ratio?
Answer: dihybrid cross (F2) with independently assorting,
completely dominant genes
Section: 3.3
32) Under what conditions does one expect a 1:1:1:1 ratio?
Answer: This occurs in a cross involving doubly
heterozygous individuals crossed to fully recessive individuals. The genes
involved assort independently.
Section: 3.3
33) What conditions are likely to apply if the progeny from the
cross AaBb X AaBb appear in the
9:3:3:1 ratio?
Answer: complete dominance, independent assortment, no
gene interaction
Section: 3.3
34) How many kinds of gametes will be expected from an
individual with the genotype PpCcTTRr?
Answer: 8
Section: 3.4
35) For the purposes of this question, assume that being
Rh+ is a consequence of D and
that Rh- individuals are dd.
The ability to taste phenylthiocarbamide (PTC) is determined by the gene
symbolized T (tt are nontasters).
A female whose mother was Rh- has the MN blood group, is Rh+ and a nontaster
of PTC, and is married to a man who is MM, Rh-, and a nontaster. List the
possible genotypes of their children. Assume that all the loci discussed in
this problem are autosomal and independently assorting.
Answer: MMDdtt,
MMddtt, MNDdtt, MNddtt
Section: 3.4
36) Two organisms, AABBCCDDEE and aabbccddee, are mated to
produce an F1 that is self-fertilized. If the capital letters represent
dominant, independently assorting alleles:
(a) How many different genotypes will occur in the F2?
(b) What proportion of the F2 genotypes will be recessive
for all five loci?
(c) Would you change your answers to part (a) and/or part (b) if
the initial cross occurred between AAbbCCddee X aaBBccDDEE parents?
(d) Would you change your answers to part (a) and/or part (b) if
the initial cross occurred between AABBCCDDEE X aabbccddEE parents?
Answer:
(a) 35 = 243
(b) 1/243
(c) no
(d) yes
Section: 3.4
37) Assuming independent assortment, what proportion of the
offspring of the cross AaBbCcDd X AabbCCdd will have the aabbccdd genotype?
Answer: zero
Section: 3.4
38) How many different types of gametes can be produced by an
individual with the genotype AABbCCddEeFf?
Answer: 23 = 8
Section: 3.4
39) What is the probability of flipping a penny and a nickel and
obtaining one head and one tail?
Answer: 1/2 (apply the “sum law”)
Section: 3.7
40) Among dogs, short hair is dominant to long hair and dark
coat color is dominant to white (albino) coat color. Assume that these two coat
traits are caused by independently segregating gene pairs. For each of the
crosses given below, write the most probable genotype (or genotypes if more
than one answer is possible) for the parents. It is important that you select a
realistic symbol set and define each symbol below.
Parental
Phenotypes
Phenotypes of Offspring
Short
Long
Short Long
Dark
Dark
Albino Albino
(a) dark, short X dark,
long
26
24
0
0
(b) albino, short X albino,
short
0
0
102
33
(c) dark, short X albino,
short
16
0
16
0
(d) dark, short X dark,
short
175
67
61
21
Assume that for cross (d), you were interested in determining
whether fur color follows a 3:1 ratio. Set up (but do not complete the
calculations) a Chi-square test for these data [fur color in cross (d)].
Answer: Let A =
dark, a =
albino and L =
short, l =
long
(a) AALl X AAll or AALl X Aall
(b) aaLl X aaLl
(c) AaLL X aaLL or AaLl X aaLL or AaLL X aaLl
(d) AaL X AaLl
χ2 = Σ = (242 – 243)2 /243 + (82 – 81)2 /81
Section: 3.8
41) In what ways is sample size related to statistical testing?
Answer: By increasing sample size, one increases the reliability
of the statistical test and decreases the likelihood of erroneous conclusions
from chance fluctuations in the data.
Section: 3.8
42) In a Chi-square analysis, what condition causes one to
reject (fail to accept) the null hypothesis?
Answer: usually when the probability value is less than
0.05
Section: 3.8
43) If one is testing a goodness of fit to a 9:3:3:1 ratio, how
many degrees of freedom would be associated with the Chi-square analysis?
Answer: number of classes minus 1 = 3
Section: 3.8
44) Assume that a Chi-square test was conducted to test the
goodness of fit to a 9:3:3:1 ratio and a Chi-square value of 10.62 was
obtained. Should the null hypothesis be accepted?
Answer: no
Section: 3.8
45) Assume that a Chi-square test was conducted to test the
goodness of fit to a 3:1 ratio and that a Chi-square value of 2.62 was
obtained. Should the null hypothesis be accepted? How many degrees of freedom
would be associated with this test of significance?
Answer: yes; 1
Section: 3.8
46) Assume that a Chi-square test provided a probability value
of 0.02. Should the null hypothesis be accepted?
Answer: no
Section: 3.8
47) Assume that a cross is made between a heterozygous tall pea
plant and a homozygous short pea plant. Fifty offspring are produced in the
following frequency:
30 = tall
20 = short
(a) What frequency of tall and short plants is expected?
(b) To test the goodness of fit between the observed and
expected values, provide the needed statement of the null hypothesis.
(c) Compute a Chi-square value associated with the appropriate
test of significance.
(d) How many degrees of freedom are associated with this test of
significance?
Answer:
(a) 1:1 (25 tall and 25 short)
(b) The deviations from a 1:1 ratio (25 tall and 25 short) are
due to chance.
(c) χ2 = 2
(d) 1
Section: 3.8
48) In a Chi-square test, as the value of the χ2 increases,
the likelihood of rejecting the null hypothesis ________.
Answer: increases
Section: 3.8
49) In studies of human genetics, usually a single individual
brings the condition to the attention of a scientist or physician. When
pedigrees are developed to illustrate transmission of the trait, what term is
used to refer to this individual?
Answer: proband
Section: 3.9
50) Mendel’s Law of Segregation is supported by a 1:1 testcross
ratio.
Answer: TRUE
Section: 3.2
51) To test Mendel’s Law of Segregation, the experimenter needs
a minimum of two contrasting forms of a gene.
Answer: TRUE
Section: 3.2
52) A 1:1 phenotypic ratio is expected from a monohybrid
testcross with complete dominance.
Answer: TRUE
Section: 3.2
53) Assuming complete dominance, a 3:1 phenotypic ratio is
expected from a monohybrid sib or self-cross.
Answer: TRUE
Section: 3.2
54) A 9:3:3:1 phenotypic ratio is expected from a dihybrid
testcross.
Answer: FALSE
Section: 3.3
55) Mendel’s postulate of independent assortment is supported by
a 1:1:1:1 testcross ratio.
Answer: TRUE
Section: 3.3
56) Mendel’s discoveries were well received and understood by
his contemporaries.
Answer: FALSE
Section: 3.5
57) The nonfunctional form of a gene is called a wild-type
allele.
Answer: FALSE
Section: 3.5
58) A gene can have a maximum of two alleles.
Answer: FALSE
Section: 3.5
Essentials of Genetics, 8e (Klug)
Chapter 4 Modification of Mendelian Ratios
1) A mutation in a gene often results in a reduction of the
product of that gene. The term for this type of mutation is ________.
1. A)
codominance
2. B)
incomplete dominance
3. C)
gain of function
4. D)
multiple allelism
5. E)
loss of function or null (in the case of complete loss)
Answer: E
Section: 4.1
2) With incomplete dominance, a likely ratio resulting from a
monohybrid cross would be ________.
1. A)
3:3
2. B)
1:2:2:4
3. C)
1:2:1
4. D)
9:3:3:1
5. E)
3:1
Answer: C
Section: 4.3
3) The presence of more than two alternative forms of a given
gene would be called ________.
1. A)
multiple alleles
2. B)
alternation of generations
3. C)
codominance
4. D)
incomplete dominance
5. E)
hemizygosity
Answer: A
Section: 4.5
4) A condition in which one gene pair masks the expression of a
nonallelic gene pair is called ________.
1. A)
codominance
2. B)
epistasis
3. C)
dominance
4. D)
recessiveness
5. E)
additive alleles
Answer: B
Section: 4.8
5) Typical ratios resulting from epistatic interactions in
dihybrid crosses would be ________.
1. A)
9:3:3:1, 1:2:1
2. B)
1:1:1:1, 1:4:6:4:1
3. C)
9:3:4, 9:7
4. D)
1:2:2:4:1:2:1:2:1, 1:2:1
5. E)
3:1, 1:1
Answer: C
Section: 4.8
6) With which of the following would hemizygosity most likely be
associated?
1. A) codominance
2. B)
incomplete dominance
3. C)
trihybrid crosses
4. D)
X-linked inheritance
5. E)
sex-limited inheritance
Answer: D
Section: 4.11
7) Because of the mechanism of sex determination, males of many
species can be neither homozygous nor heterozygous. Such males are said to be
________.
1. A)
dominant
2. B)
hemizygous
3. C)
recessive
4. D)
complementary
5. E)
None of the answers listed is correct.
Answer: B
Section: 4.11
8) How many different alleles can a gene have?
Answer: Theoretically, an extremely large number of
possibilities exist. Various bases could change, giving a variety of alleles,
and combinations of those changed bases could provide additional variety.
Section: 4.1
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