Download 3.14 C: Genetic Disorders Quiz PROCTOR VERSION

PROCTOR VERSION
3.14 C: Genetic Disorders Quiz
1.
A karyotype shows the visual appearance of an individual’s chromosomes. The karyotype below
shows the chromosomes of a person with a genetic disorder.
Scientists use observable evidence to direct their questions about phenomena. For which
question would the karyotype provide the most evidence?
(A) Since the person is missing one sex chromosome, did the two homologous Y chromosomes
fail to separate as the male gamete was undergoing meiosis before fertilization?
Distractor Rationale:
This answer suggests the student may understand that nondisjunction of chromosomes can
produce a monosomy (2n-1), as evidenced by the karyotype, but does not understand that
this could not occur as described because the Y chromosome does not form a homologous
pair with another Y chromosome (as it pairs with an X chromosome in males).
(B) Since the person is missing one sex chromosome, did nondisjunction occur during meiosis
when forming gametes before fertilization?
Rationale:
This answer suggests the student understands that nondisjunction of chromosomes during
meiosis can produce a monosomy (2n-1) because a gamete with a missing chromosome (n1) can be produced, and when this gamete combines with a normal gamete (n), it produces
a monosomy (2n-1), as evidenced by the karyotype.
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PROCTOR VERSION
3.14 C: Genetic Disorders Quiz
(C) Since the person is missing one sex chromosome, possibly the Y chromosome provided by
a sperm cell, did an unfertilized egg undergo DNA replication to change from a haploid cell
to a diploid cell?
Distractor Rationale:
This answer suggests the student may understand that if a gamete replicates its DNA, it will
become a diploid cell, but does not understand that if this did occur in an egg cell, the
offspring would have two X chromosomes and the resulting ploidy would produce a 2n+1
karyotype after fertilization because the affected gamete would pair with a haploid gamete
(2n+n=3n), instead of the 2n-1 karyotype shown.
(D) Since the person is missing one sex chromosome, did the X and Y chromosomes cross over
during meiosis I to produce a nonfunctional chromosome?
Distractor Rationale:
This answer suggests the student may understand that crossing over causes genetic
reshuffling and occurs in meiosis I, but does not understand that crossing over only occurs
between homologous chromosomes (not sex chromosomes) and does not create mutations
like translocations, duplications, or deletions because it does not change the ultimate
number of chromosomes, which is needed to result in a genetic disorder involving ploidy.
Aligned to: LO 3.14 CA 3.14: Apply Math to Genetics
2.
A karyotype shows the visual appearance of an individual’s chromosomes. The karyotype below
shows a set of chromosomes found in a fertilized human egg.
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PROCTOR VERSION
3.14 C: Genetic Disorders Quiz
Which scientific question would be the most logical to ask if a scientist wanted to investigate the
cause of a genetic condition shown in the karyotype?
(A) Is this condition caused by a sex cell that completed meiosis I but not meiosis II before
fertilization?
Rationale:
This answer suggests the student understands that without meiosis II (or meiosis I) sex
cells will be diploid, not haploid, and that after fertilization, a triploid individual will be
produced because the error in the conservation of chromosome number that occurred
during meiosis II will lead to the genetic disorder (triploidy) shown in the karyotype
(2n+n=3n).
(B) Is this condition caused by nondisjunction in a pair of homologous chromosomes in one of
the sex cells before fertilization?
Distractor Rationale:
This answer suggests the student may understand that nondisjunction in homologous
chromosomes can cause extra chromosomes in sex cells and offspring, but does not
understand that this would not produce a triploidy condition because there would only be
one additional chromosome (trisomy), not an entire extra set of chromosomes (triploidy), as
shown in the karyotype.
(C) Is this condition caused by a fertilized egg that underwent DNA replication, but not mitosis or
cell division, after fertilization?
Distractor Rationale:
This answer suggests the student may understand that DNA replication without mitosis or
cell division in a cell would produce a polyploidy condition, but does not understand that
this would produce a tetraploidy condition, not the triploidy condition shown in the karyotype,
because when a diploid cell divides there are four sets of chromosomes (2n×2=4n).
(D) Is this condition caused by the fertilization of a sex cell by another sex cell that had not
undergone DNA replication before meiosis?
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PROCTOR VERSION
3.14 C: Genetic Disorders Quiz
Distractor Rationale:
This answer suggests the student may understand that if DNA replication does not occur
before meiosis, sex cells will be produced with an incorrect number of chromosomes, but
does not understand that this would not result in a triploidy offspring because the sex cell
would be ½n instead of n, which would result in an offspring that is 1½n, not the 3n offspring
shown in the karyotype.
Aligned to: LO 3.14 CA 3.14: Apply Math to Genetics
3.
Huntington’s disease is an autosomal dominant disorder. Which pedigree could represent a
family with a history of Huntington’s disease?
(A)
Distractor Rationale:
This answer suggests the student may understand that dominant traits are expressed if an
individual has at least one dominant allele (right side of pedigree), but does not understand
that dominant traits cannot “skip a generation,” because a dominant allele will always be
expressed, unlike a recessive allele, which can be masked by a dominant allele and can
reappear in the next generation if two recessive alleles are passed down (left side of
pedigree). The student may not understand how to apply a Punnett square to determine
the mode of inheritance observed in the pedigree.
(B)
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PROCTOR VERSION
3.14 C: Genetic Disorders Quiz
Distractor Rationale:
This answer suggests the student may understand that dominant traits appear about 50% of
the time in successive generations, but does not understand that dominant traits cannot
“skip a generation,” because a dominant allele will always be expressed, unlike a recessive
allele, which can be masked by a dominant allele and can reappear in the next generation if
two recessive alleles are passed down (left side of pedigree). The student may not
understand how to apply a Punnett square to determine the mode of inheritance observed
in the pedigree.
(C)
Distractor Rationale:
This answer suggests the student may understand that dominant traits appear in every
successive generation and do not have to be passed to future generations (right side of
pedigree), but does not understand that dominant traits cannot “skip a generation,”
because a dominant allele will always be expressed, unlike a recessive allele, which can be
masked by a dominant allele and can reappear in the next generation if two recessive alleles
are passed down (left side of pedigree). The student may not understand how to apply a
Punnett square to determine the mode of inheritance observed in the pedigree.
(D)
Rationale:
This answer suggests the student understands that a dominant trait can be passed to an
offspring if at least one parent expresses the dominant phenotype, but that the dominant trait
cannot appear in an offspring if both parents do not express the dominant phenotype (and
therefore do not have the dominant allele), as seen in the last generation in the pedigree.
Aligned to: LO 3.14 CA 3.14: Apply Math to Genetics
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PROCTOR VERSION
3.14 C: Genetic Disorders Quiz
4.
A scientist is studying the pedigrees of four families in order to identify a family that may have a
sex-linked, recessive genetic disorder.
Which statement provides the best justification for identifying a family as having a sex-linked
recessive genetic disorder based on its pedigree?
(A) Pedigree 1 shows a recessive, sex-linked disorder, because a mother passes the trait down
to her sons in generation II, and they pass the trait on to their sons in generation III.
Distractor Rationale:
This answer suggests the student may understand that sex-linked, recessive traits are
generally passed from mother to son and are mostly observed in males, but does not
understand that these traits cannot be passed from father to son because the son does not
inherit an X chromosome from his father; thus the student may mistakenly believe that the
son could inherit an X or Y chromosome from either parent. The student may not
understand how to apply a Punnett square to determine the mode of inheritance of a trait
that shows the pattern of an affected father (X´Y) not passing the trait to his son (and an
affected daughter not being produced unless a father is also affected), which is only seen in
pedigree 3.
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PROCTOR VERSION
3.14 C: Genetic Disorders Quiz
The prime symbol (´) denotes a chromosome carrying the mutant allele.
(B) Pedigree 2 shows a recessive, sex-linked disorder, because the trait affects mostly males,
skips generations, and is carried, but not expressed, by females.
Distractor Rationale:
This answer suggests the student may understand that sex-linked, recessive traits are
mostly expressed in males, but does not understand that these traits cannot be observed
in a daughter with a father who does not express the condition, as seen in the affected
daughter in generation III, because the daughter always inherits the X chromosome from her
father and the father must have the condition in order to pass it on to his daughter. The
student may not understand how to apply a Punnett square to determine the mode of
inheritance of a trait that shows the pattern of an affected father (X´Y) not passing the trait to
his son and an affected daughter (X´X´) not being produced unless a father is also affected,
which is only seen in pedigree 3.
The prime symbol (´) denotes a chromosome carrying the mutant allele.
(C) Pedigree 3 shows a recessive, sex-linked disorder, because the trait affects mostly males
and, since it is on the X chromosome, it is never passed from father to son.
Rationale:
This answer suggests the student understands that sex-linked, recessive traits are passed
on the X chromosome, so females often carry, but do not normally express, the phenotype
(unless both X chromosomes are affected), and males inherit the condition from their
mother, not their father.
(D) Pedigree 4 shows a recessive, sex-linked disorder, because the trait affects mostly males,
skips generations, and is passed from mother to son.
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PROCTOR VERSION
3.14 C: Genetic Disorders Quiz
Distractor Rationale:
This answer suggests the student may understand that sex-linked, recessive traits are
mostly expressed in males, but does not understand that these traits cannot be observed
in a daughter with a father who does not express the condition because the daughter always
inherits the X chromosome from her father and the father must have the condition in order to
pass it on to his daughter. The student may not understand how to apply a Punnett square
to determine the mode of inheritance of a trait that shows the pattern of an affected father
(X´Y) not passing the trait to his son and an affected daughter (X´X´) not being produced
unless a father is also affected, which is only seen in pedigree 3.
The prime symbol (´) denotes a chromosome carrying the mutant allele.
Aligned to: LO 3.14 CA 3.14: Apply Math to Genetics
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