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General
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Quiz Ch. 15 Chromosomal Basis of Inheritance
Revised March 11, 2005
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Practice quiz questions selected from the test bank provided
by text book publisher. For Word version.
Some questions refer to images that require you click on a hyperlink
to see.
1. If inheritance of a human trait is sex-linked (on the X chromosome)
and recessive, any of the following could
result EXCEPT that
a. expression of the trait might "skip" a
generation.
b. the trait could be more common in females
than males.
c. all females might become homozygous for
the trait.
d. the gene for the trait might mutate to
a dominant allele.
e. females could be a mosaic of two cell types.
2. Which of these chromosome
alterations is best described as a gene duplication?
Click on link above to see Figure.
a.
b.
c.
d.
e.
3. What do all males inherit from their mother?
a. mitochondrial DNA
b. X chromosome
c. male-pattern baldness trait
d. mitochondrial DNA and X chromosome
e. mitochondria DNA, X chromosome, and male-pattern
baldness trait
4. What does independent assortment refer to?
a. the replication of each DNA thread independently
during the S Phase
b. the random arrangement of chromosomal tetrads
at metaphase I
c. the separation of chromatids at anaphase
II
d. the random arrangement of gene loci on
a chromosome
e. the fact that any pair of chromatids in
a tetrad can cross over
5. A Barr body is normally found in the nucleus of which kind
of human
cell?
a. unfertilized egg cells only
b. sperm cells only
c. somatic cells of a female only
d. somatic cells of a male only
e. both male and female somatic cells
6. The particular position of a gene on a chromosome is known
as a(n)
a. allele.
b. tetrad.
c. chiasma.
d. locus.
e. map distance.
7. The frequency of crossing over between any two linked genes is
a. more likely if they are recessive.
b. difficult to predict.
c. determined by their relative dominance.
d. the same as if they were not linked.
e. greater the further apart they are.
8. A recessive allele on the X chromosome is responsible for red-green
color blindness in humans. A normal vision
woman whose father is
color-blind marries a color-blind male. What
is the probability that
this couple's son will be color-blind?
a. 0%
b. 25%
c. 50%
d. 75%
e. 100%
9. A man who carries an X-linked allele will pass it on to
a. all of his daughters.
b. half of his daughters.
c. all of his sons.
d. half of his sons.
e. all of his children.
10. In cats, black color is caused by an X-linked allele; the
other
allele at this locus causes orange color.
The heterozygote is
tortoise-shell. What kinds of offspring would
you expect from the
cross of a black female and an orange male?
a. tortoise-shell female; tortoise-shell male
b. black female; orange male
c. orange female; orange male
d. tortoise-shell female; black male
e. orange female; black male
---------------OMIT 11, 12, 13---------------
Use the information below to answer the following
question(s).
An achondroplastic dwarf man (heterozygous) with normal vision marries
a
color-blind woman of normal height. The man's father was 6 feet
tall, and both the woman's parents were of average height.
Achondroplastic dwarfism is autosomal dominant (i.e. like Brown
Eyes), and red-green color
blindness is X-linked recessive. Hint:
first, write out all possible genotypes and
phenotypes for each trait, then write out the genotypes of each parent,
then do seperate
Punnett squares for each trait, and then multiply the probabilities.
11. How many of their female children might
be expected to be
color-blind dwarfs?
a. all
b. none
c. half
d. one out of four
e. three out of four
12. How many of their male children would
be color-blind and normal
height?
a. all
b. none
c. half
d. one out of four
e. three out of four
13. They have a daughter who is a dwarf with
normal color vision. What
is the probability that she is heterozygous for
both genes?
a. 0
b. 0.25
c. 0.50
d. 0.75
e. 1.00
14. If a human interphase nucleus contained three Barr bodies
it can be
assumed that the person
a. has a normal female genotype.
b. is a male.
c. must have 4 X chromosomes.
d. has Turner syndrome.
e. has Down syndrome.
15. If a karyotype shows an individuals with the XXY genotype, then
the
individual is most likely
a. a normal female
b. a normal male.
c. an individual with Kleinefelter syndrome.
d. an individual with Turner syndrome.
e. a meta-female.
16. The diploid chromosome number in honeybees is 32. What is
the number
of chromosomes in the somatic cells of a male
honeybee?
a. 4
b. 8
c. 16
d. 32
e. 64
17. A collection of Cassette tapes or compact disks contains a series
of distinct pieces
of electrical or physical information that
are interpreted by a tape
player or compact disk player, resulting in
music. If the
information that produces a song is analogous
to a gene, and the
tape or compact disk is analogous to a chromosome,
then "linked
genes" are analogous to
a. the length of the songs on the tape or
disk.
b. songs on the same tape or disk.
c. the volume of the music on the tape or
disk.
d. the tempo of the music on the tape or disk.
e. the informational content of the songs
on the tape or disk.
18. The following figure shows five genes on a pair of duplicated
chromosomes.
The paternal version is shown in black, maternal in red. Crossing
over frequently occurs
between maternal and paternal versions of chromosomes during meiosis.

Between which two genes would you expect the highest frequency of
recombination? Stated another way, if crossing over occurs between
the black strand and
the red strand during meiosis, which two linked-genes are most likely
to wind up
separated by crossing over?
a. 1 and 3
b. 1 and 2
c. 2 and 4
d. 3 and 4
e. 1 and 4
19. The karyotype of a Down syndrome individual will show
a. trisomy of the X chromosome
b. cells that are monosomic for chromosome 22
c. trisomy of chromosome 21
d. XXY
e. trisomy of chromosome 17
END
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