Starting with a fertilized egg (zygote), a series of five cell
divisions would produce an early embryo with how many cells?
A)
4
B) 8
C) 16
D) 32
E) 64
D
If there are 20 chromatids in a cell, how many centromeres are there?
A) 10
B) 20
C) 30
D) 40
E) 80
B
In eukaryotic cells, chromosomes are composed of DNA
A) and RNA.
B) only.
C) and proteins.
D) and phospholipids.
C
What is produced if a cell divides by mitosis but does not undergo cytokinesis?
A) two cells, one cell containing two nuclei and a second cell
without a nucleus
B) two cells, each cell with half of the
genetic material of the parent cell
C) one cell with one nucleus
containing half of the genetic material of the parent cell
D) one cell with two nuclei, each identical to the nucleus of the parent cell
D
Humans produce skin cells by mitosis and gametes by meiosis. The
nuclei of skin cells produced by mitosis will have
A) half as
much DNA as the nuclei of gametes produced by meiosis.
B) the
same amount of DNA as the nuclei of gametes produced by meiosis.
C) twice as much DNA as the nuclei of gametes produced by
meiosis.
D) four times as much DNA as the nuclei of gametes
produced by meiosis.
C
Compared to most prokaryotic cells, eukaryotic cells typically have
A) more DNA molecules and larger genomes.
B) the same number
of DNA molecules but larger genomes.
C) the same number of DNA
molecules and similarly sized genomes.
D) fewer DNA molecules but larger genomes.
E) fewer DNA molecules and smaller genomes.
A
At which phase are centrioles beginning to move apart in animal cells?
A) telophase
B) anaphase
C) prometaphase
D) metaphase
E) prophase
E
If there are 20 centromeres in a cell at anaphase, how many
chromosomes are there in each daughter cell following
cytokinesis?
A) 10
B) 20
C) 30
D) 40
E) 80
A
Where do the microtubules of the spindle originate during mitosis in animal cells?
A) centromere
B) centrosome
C) centriole
D) chromatid
E) kinetochore
B
Taxol is an anticancer drug extracted from the Pacific yew tree. In
animal cells, Taxol disrupts microtubule formation by binding to
microtubules and accelerating their assembly from the protein
precursor tubulin. Surprisingly, this stops mitosis. Specifically,
Taxol must affect
A) the formation of the mitotic spindle.
B) anaphase.
C) formation of the centrioles.
D) chromatid
assembly.
E) the S phase of the cell cycle.
A
Which of the following are primarily responsible for cytokinesis in
plant cells but not in animal cells?
A) kinetochores
B)
Golgi-derived vesicles
C) actin and myosin
D) centrioles and centromeres
E)
tubulin and dynein
B
Movement of the chromosomes during anaphase would be most affected by
a drug that prevents
A) nuclear envelope breakdown.
B)
cell wall formation.
C) elongation of microtubules.
D) shortening of
microtubules.
E) formation of a cleavage furrow.
D
Measurements of the amount of DNA per nucleus were taken on a large
number of cells from a growing fungus. The measured DNA levels ranged
from 3 to 6 picograms per nucleus. In which stage of the cell cycle
did the nucleus contain 6 picograms of DNA?
A) G0
B)
G1
C) S
D) G2
E) M
D
A group of cells is assayed for DNA content immediately following
mitosis and is found to have an average of 8 picograms of DNA per
nucleus. How many picograms would be found at the end of S and the end
of G2?
A) 8; 8
B) 8; 16
C) 16; 8
D) 16; 16
E) 12; 16
D
The beginning of anaphase is indicated by which of the following?
A) Chromatids lose their kinetochores.
B) Cohesin attaches the
sister chromatids to each other.
C) Cohesin is cleaved enzymatically.
D) Kinetochores attach to the metaphase plate.
E) Spindle microtubules begin to polymerize.
C
During which phase of mitosis do the chromatids become chromosomes?
A) telophase
B) anaphase
C) prophase
D) metaphase
E) cytokinesis
B
What is a cleavage furrow?
A) a ring of vesicles forming a cell
plate
B) the separation of divided prokaryotes
C) a groove
in the plasma membrane between daughter nuclei
D) the metaphase
plate where chromosomes attach to the spindle
E) the space that
is created between two chromatids during anaphase
C
Using which of the following techniques would enable your lab group
to distinguish between a cell in G2 and a cell from the same organism
in G1?
A) fluorescence microscopy
B) electron microscopy
C) spectrophotometry
D) radioactive-labeled nucleotides
E) labeled kinetochore proteins
D
You have the technology necessary to measure each of the following in
a sample of animal cells: chlorophylls, organelle density, picograms
of DNA, cell wall components, and enzymatic activity. Which would you
expect to increase significantly from M to G1?
A) organelle
density and enzymatic activity
B) cell wall components and DNA
C) chlorophyll and cell walls
D) organelle density and cell walls
E) chlorophyll and DNA
A
A plant-derived protein known as colchicine can be used to poison
cells by blocking the formation of the spindle. Which of the following
would result if colchicine is added to a sample of cells in G2?
A) The cells would immediately die.
B) The cells would be unable
to begin M and stay in G2.
C) The chromosomes would coil and
shorten but have no spindle to which to attach.
D) The
chromosomes would segregate but in a disorderly pattern.
E) Each
resultant daughter cell would also be unable to form a spindle.
C
Motor proteins require which of the following to function in the
movement of chromosomes toward the poles of the mitotic spindle?
A) intact centromeres
B) a microtubule-organizing center
C) a kinetochore attached to the metaphase plate
D) ATP as an energy source
E) synthesis of cohesin
D
When a cell is in late anaphase of mitosis, which of the following will we see?
A) a clear area in the center of the cell
B) chromosomes
clustered at the poles
C) individual chromatids beginning to
separate from one another
D) chromosomes clustered tightly at the center
E) breaking down of the nuclear envelope
A
Cells from advanced malignant tumors often have very abnormal
chromosomes as well as an abnormal number of chromosomes. What might
explain the association between malignant tumors and chromosomal
abnormalities?
A) Cancer cells are no longer density dependent.
B) Cancer cells are no longer anchorage dependent.
C) Cell
cycle checkpoints are not in place to stop cells with chromosome abnormalities.
D) Chromosomally abnormal cells still have normal metabolism.
E) Transformation introduces new chromosomes into cells.
C
Which is the first checkpoint in the cell cycle where a cell will be
caused to exit the cycle if this point is not passed?
A)
G0
B) G1
C) G2
D) S
E) previous M
B
Which of the following is released by platelets in the vicinity of an injury?
A) PDGF
B) MPF
C) protein kinase
D) cyclin
E) Cdk
A
Which of the following is a protein synthesized at specific times
during the cell cycle that associates with a kinase to form a
catalytically active complex?
A) PDGF
B) MPF
C) protein kinase
D) cyclin
E) Cdk
D
Which of the following is a protein maintained at constant levels
throughout the cell cycle that requires cyclin to become catalytically
active?
A) PDGF
B) MPF
C) protein kinase
D) cyclin
E) Cdk
E
Which of the following triggers the cell's passage past the G2 checkpoint into mitosis? A) PDGF
B) MPF
C) protein kinase
D) cyclin
E) Cdk
B
The cyclin component of MPF is destroyed toward the end of which phase?
A) G0
B) G1
C) S
D) G2
E) M
E
Proteins that are involved in the regulation of the cell cycle, and
that show fluctuations in concentration during the cell cycle, are
called
A) ATPases.
B) kinetochores.
C) kinases.
D) estrogen receptors.
E) cyclins.
E
The MPF protein complex turns itself off by
A) activating a
process that destroys cyclin components.
B) activating an enzyme that stimulates cyclin.
C) binding to
chromatin.
D) exiting the cell.
E) activating the
anaphase-promoting complex.
A
Density-dependent inhibition is explained by which of the
following?
A) As cells become more numerous, they begin to
squeeze against each other, restricting their size and ability to
produce control factors.
B) As cells become more numerous, the
cell surface proteins of one cell contact the adjoining cells and they
stop dividing.
C) As cells become more numerous, the protein
kinases they produce begin to compete with each other, such that the
proteins produced by one cell essentially cancel those produced by its
neighbor.
D) As cells become more numerous, more and more of
them enter the S phase of the cell cycle.
E) As cells become more numerous, the level of waste products increases, eventually slowing down metabolism.
B
Which of the following is true concerning cancer cells?
A) They
do not exhibit density-dependent inhibition when growing in
culture.
B) When they stop dividing, they do so at random points
in the cell cycle.
C) They are not subject to cell cycle
controls.
D) When they stop dividing, they do so at random
points in the cell cycle, and they are not subject to cell cycle
controls.
E) When they stop dividing, they do so at random
points in the cell cycle; they are not subject to cell cycle controls;
and they do not exhibit density-dependent inhibition when growing in culture.
E
Which of the following describes cyclin-dependent kinase (Cdk)?
A) Cdk is inactive, or "turned off," in the presence of
cyclin.
B) Cdk is present throughout the cell cycle.
C)
Cdk is an enzyme that attaches phosphate groups to other
proteins.
D) Cdk is inactive, or "turned off," in the
presence of cyclin and it is present throughout the cell cycle.
E) Cdk is present throughout the cell cycle and is an enzyme that attaches phosphate groups to other proteins.
E
Besides the ability of some cancer cells to overproliferate, what
else could logically result in a tumor?
A) enhanced anchorage
dependence
B) changes in the order of cell cycle stages
C) lack of appropriate cell death
D) inability to form
spindles
E) inability of chromosomes to meet at the metaphase plate
C
Why do neurons and some other specialized cells divide infrequently?
A) They no longer have active nuclei.
B) They no longer carry
receptors for signal molecules.
C) They have been shunted into G0.
D) They can no longer bind Cdk to cyclin.
E) They show a drop in MPF concentration.
C
Which of the following most accurately describes a cyclin?
A)
It is present in similar concentrations throughout the cell cycle.
B) It is activated to phosphorylate by complexing with a Cdk.
C) It decreases in concentration when MPF activity increases.
D)
It activates a Cdk molecule when it is in sufficient concentration.
E) It activates a Cdk when its concentration is decreased.
D
All cell cycle checkpoints are similar in which way?
A) They
respond to the same cyclins.
B) They utilize the same
Cdks.
C) They give the go-ahead signal to progress to the next checkpoint.
D) They each have only one cyclin/Cdk complex.
E) They activate or inactivate other proteins.
C
At the M phase checkpoint, the complex allows for what to occur?
A) Separase enzyme cleaves cohesins and allows chromatids to separate.
B) Cohesins alter separase to allow chromatids to separate.
C)
Kinetochores are able to bind to spindle microtubules.
D) All
microtubules are made to bind to kinetochores.
E) Daughter cells
are allowed to pass into G1.
A
Anchorage dependence of animal cells in vitro or in vivo depends on which of the following?
A) attachment of spindle fibers to centrioles
B) response of
the cell cycle controls to signals from the plasma membrane
C)
the absence of an extracellular matrix
D) the binding of cell-surface phospholipids to those of adjoining cells
E) the binding of cell-surface phospholipids to the substrate
B
Researchers began a study of a cultured cell line. Their preliminary
observations showed them that the cell line did not exhibit either
density-dependent inhibition or anchorage dependence. What could they
conclude right away?
A) The cells originated in the nervous system.
B) The cells are unable to form spindle microtubules.
C) The
cells have altered series of cell cycle phases.
D) The cells
show characteristics of tumors.
E) The cells were originally
derived from an elderly organism.
D
For a chemotherapeutic drug to be useful for treating cancer cells,
which of the following is most desirable?
A) It is safe enough
to limit all apoptosis.
B) It does not alter metabolically
active cells.
C) It only attacks cells that are density dependent.
D) It interferes with cells entering G0.
E) It interferes with
rapidly dividing cells.
E
You have a series of cells, all of which were derived from tumors,
and you first need to find out which ones are malignant. What could
you do?
A) See which ones are not overproliferating.
B)
Find out which ones have a higher rate of apoptosis.
C) Karyotype samples to look for unusual size and number of chromosomes.
D) Measure metastasis.
E) Time their cell cycles.
C
These protists are intermediate in what sense?
A) They
reproduce by binary fission in their early stages of development and
by mitosis when they are mature.
B) They never coil up their
chromosomes when they are dividing.
C) They use mitotic division
but only have circular chromosomes.
D) They maintain a nuclear
envelope during division.
E) None of them form spindles.
D
What is the most probable hypothesis about these intermediate forms
of cell division?
A) They represent a form of cell reproduction
that must have evolved completely separately from those of other
organisms.
B) They demonstrate that these species are not
closely related to any of the other protists and may well be a
different kingdom.
C) They rely on totally different proteins
for the processes they undergo.
D) They may be more closely
related to plant forms that also have unusual mitosis.
E) They
show some but not all of the evolutionary steps toward complete mitosis.
E
Which of the following questions might be answered by such a method?
A) How many cells are produced by the culture per hour?
B)
What is the length of the S phase of the cell cycle?
C) When is
the S chromosome synthesized?
D) How many picograms of DNA are made per cell cycle?
E) When do spindle fibers attach to chromosomes?
B
The research team used the setup to study the incorporation of labeled nucleotides into a culture of lymphocytes and found that the lymphocytes incorporated the labeled nucleotide at a significantly higher level after a pathogen was introduced into the culture. They concluded that
A) the presence of the pathogen made the experiment too contaminated
to trust the results.
B) their tissue culture methods needed to
be relearned.
C) infection causes lymphocytes to divide more
rapidly.
D) infection causes cell cultures in general to
reproduce more rapidly.
E) infection causes lymphocyte cultures
to skip some parts of the cell cycle.
C
Through a microscope, you can see a cell plate beginning to develop
across the middle of a cell and nuclei forming on either side of the
cell plate. This cell is most likely
A) an animal cell in the
process of cytokinesis.
B) a plant cell in the process of cytokinesis.
C) an animal cell in the S phase of the cell cycle.
D) a bacterial cell dividing.
E) a plant cell in metaphase.
B
In the cells of some organisms, mitosis occurs without cytokinesis.
This will result in A) cells with more than one nucleus.
B)
cells that are unusually small.
C) cells lacking nuclei.
D) destruction of chromosomes.
E) cell cycles lacking an S phase.
A
Which of the following does not occur during mitosis?
A) condensation of the chromosomes
B) replication of the
DNA
C) separation of sister chromatids
D) spindle formation
E) separation of the spindle poles
B
A particular cell has half as much DNA as some other cells in a
mitotically active tissue. The cell in question is most likely
in
A) G1.
B) G2.
C) prophase.
D) metaphase.
E) anaphase.
A
The drug cytochalasin B blocks the function of actin. Which of the
following aspects of the animal cell cycle would be most disrupted by
cytochalasin B?
A) spindle formation
B) spindle attachment
to kinetochores
C) DNA synthesis
D) cell elongation during anaphase
E)
cleavage furrow formation and cytokinesis
E
If a horticulturist breeding gardenias succeeds in having a single
plant with a particularly desirable set of traits, which of the
following would be her most probable and efficient route to
establishing a line of such plants?
A) Backtrack through her
previous experiments to obtain another plant with the same traits.
B) Breed this plant with another plant with much weaker
traits.
C) Clone the plant asexually to produce an identical
one.
D) Force the plant to self-pollinate to obtain an identical
one.
E) Add nitrogen to the soil of the offspring of this plant
so the desired traits continue.
C
Which of the following defines a genome?
A) representation of a
complete set of a cell's polypeptides
B) the complete set of an organism's polypeptides
C) the
complete set of a species' polypeptides
D) a karyotype
E)
the complete set of an organism's genes
E
Which is the smallest unit containing the entire human genome?
A) one human somatic cell
B) one human chromosome
C) all
of the DNA of one human
D) the entire human population
E) one human gene
A
If an organism is diploid and a certain gene found in the organism has 18 known alleles (variants), then any given organism of that species can/must have which of the following?
A) at most, 2 alleles for that gene
B) up to 18 chromosomes
with that gene
C) up to 18 genes for that trait
D) a haploid number of 9
chromosomes
E) up to, but not more than, 18 different traits
A
Which of the following is a true statement about sexual vs. asexual
reproduction?
A) Asexual reproduction, but not sexual
reproduction, is characteristic of plants and fungi.
B) In sexual reproduction, individuals transmit 50% of their genes to each of their offspring.
C) In asexual reproduction, offspring are produced by fertilization
without meiosis.
D) Sexual reproduction requires that parents be
diploid.
E) Asexual reproduction produces only haploid offspring.
B
At which stage of mitosis are chromosomes usually photographed in the
preparation of a karyotype?
A) prophase
B) metaphase
C) anaphase
D) telophase
E) interphase
B
Which of the following is true of a species that has a chromosome
number of 2n = 16? A) The species is diploid with 32 chromosomes per
cell.
B) The species has 16 sets of chromosomes per cell.
C) Each cell has eight homologous pairs.
D) During the S phase of the cell cycle there will be 32 separate chromosomes.
E) A gamete from this species has four chromosomes.
C
Eukaryotic sexual life cycles show tremendous variation. Of the following elements, which do all sexual life cycles have in common?
- Alternation of generations
- Meiosis
- Fertilization
- Gametes
- Spores
A) I, IV, and V
B) I, II, and IV
C) II, III, and
IV
D) II, IV, and V
E) I, II, III, IV, and V
C
Which of these statements is false?
A) In humans, each of the
22 maternal autosomes has a homologous paternal chromosome.
B) In humans, the 23rd pair, the sex chromosomes, determines whether
the person is female (XX) or male (XY).
C) Single, haploid (n)
sets of chromosomes in ovum and sperm unite during fertilization,
forming a diploid (2n), single-celled zygote.
D) At sexual
maturity, ovaries and testes produce diploid gametes by meiosis.
E) Sexual life cycles differ with respect to the relative timing of
meiosis and fertilization.
D
Referring to a plant's sexual life cycle, which of the following
terms describes the process that leads directly to the formation of
gametes?
A) sporophyte meiosis
B) gametophyte mitosis
C) gametophyte meiosis
D) sporophyte mitosis
E)
alternation of generations
B
Which of the following is an example of alternation of
generations?
A) A grandparent and grandchild each have dark
hair, but the parent has blond hair.
B) A diploid plant
(sporophyte) produces, by meiosis, a spore that gives rise to a
multicellular, haploid pollen grain (gametophyte).
C) A diploid
animal produces gametes by meiosis, and the gametes undergo
fertilization to produce a diploid zygote.
D) A haploid mushroom
produces gametes by mitosis, and the gametes undergo fertilization,
which is immediately followed by meiosis.
E) A diploid cell
divides by mitosis to produce two diploid daughter cells, which then
fuse to produce a tetraploid cell.
B
The human X and Y chromosomes
A) are both present in every
somatic cell of males and females alike.
B) are about the same
size and have approximately the same number of genes.
C) are almost entirely homologous, despite their different
names.
D) include genes that determine an individual's
sex.
E) are called autosomes.
D
Which of these is a karyotype?
A) a natural cellular
arrangement of chromosomes in the nucleus
B) a display of all the cell types in an organism
C) organized
images of a cell’s chromosomes
D) the appearance of an
organism
E) a display of a cell’s mitotic stages
C
Mitosis is commonly found in all of the following except
A) a haploid animal cell.
B) a diploid animal cell.
C) a
haploid plant cell.
D) a diploid plant cell.
A
Which of these is a way that the sexual life cycle increases genetic variation in a species?
A) by allowing crossing over
B) by allowing an increase in
cell number
C) by increasing gene stability
D) by conserving chromosomal gene order
E) by decreasing mutation frequency
A
A given organism has 46 chromosomes in its karyotype. We can
therefore conclude which of the following?
A) It must be
human.
B) It must be a primate.
C) It must be an animal.
D) It must be sexually
reproducing.
E) Its gametes must have 23 chromosomes.
E
A triploid cell contains three sets of chromosomes. If a cell of a usually diploid species with 42 chromosomes per cell is triploid, this cell would be expected to have which of the following?
A) 63 chromosomes in 31 1/2 pairs
B) 63 chromosomes in 21 sets
of 3
C) 63 chromosomes, each with three chromatids
D) 21 chromosome
pairs and 21 unique chromosomes
B
Which of the following best describes a karyotype?
A) a
pictorial representation of all the genes for a species
B) a
display of each of the chromosomes of a single cell
C) the
combination of all the maternal and paternal chromosomes of a species
D) the collection of all the chromosomes in an individual
organism
E) a photograph of all the cells with missing or extra chromosomes
B
Which of the following can utilize both mitosis and meiosis in the correct circumstances?
A) a haploid animal cell
B) a diploid cell from a plant
stem
C) any diploid animal cell
D) a plantlike protist
E) an archaebacterium
D
The somatic cells of a privet shrub each contain 46 chromosomes. To
be as different as they are from human cells, which have the same
number of chromosomes, which of the following must be true?
A)
Privet cells cannot reproduce sexually.
B) Privet sex cells have chromosomes that can synapse with human
chromosomes in the laboratory.
C) Genes of privet chromosomes
are significantly different than those in humans.
D) Privet
shrubs must be metabolically more like animals than like other shrubs.
E) Genes on a particular privet chromosome, such as the X, must be on a different human chromosome, such as number 18.
C
In a human karyotype, chromosomes are arranged in 23 pairs. If we
choose one of these pairs, such as pair 14, which of the following do
the two chromosomes of the pair have in common?
A) length and
position of the centromere only
B) length, centromere position, and staining pattern only
C)
length, centromere position, staining pattern, and traits coded for by
their genes
D) length, centromere position, staining pattern, and DNA
sequences
E) They have nothing in common except they are X-shaped.
C
To view and analyze human chromosomes in a dividing cell, which of
the following is (are) required?
A) a scanning electron
microscope
B) radioactive staining
C) fluorescent staining and a transmission electron microscope
D) DNA staining and a light microscope
E) a stain particular
to human cells
D
The karyotype of one species of primate has 48 chromosomes. In a
particular female, cell division goes awry and she produces one of her
eggs with an extra chromosome (25). The most probable source of this
error would be a mistake in which of the following?
A) mitosis
in her ovary
B) metaphase I of one meiotic event
C) telophase II of one meiotic event
D) telophase I of one meiotic event
E) either anaphase I or II
E
If a cell has completed the first meiotic division and is just
beginning meiosis II, which of the following is an appropriate
description of its contents?
A) It has half the amount of DNA as
the cell that began meiosis.
B) It has the same number of
chromosomes but each of them has different alleles than another cell
from the same meiosis.
C) It has half the chromosomes but twice the DNA of the originating
cell.
D) It has one-fourth the DNA and one-half the chromosomes
as the originating cell.
E) It is identical in content to another cell from the same meiosis.
A
Which of the following might result in a human zygote with 45
chromosomes?
A) an error in either egg or sperm meiotic
anaphase
B) failure of the egg nucleus to be fertilized by the
sperm
C) fertilization of a 23 chromosome human egg by a 22
chromosome sperm of a closely related species
D) an error in the alignment of chromosomes on the metaphase plate
E) lack of chiasmata in prophase I
A
After telophase I of meiosis, the chromosomal makeup of each daughter
cell is A) diploid, and the chromosomes are each composed of a single
chromatid.
B) diploid, and the chromosomes are each composed of
two chromatids.
C) haploid, and the chromosomes are each
composed of a single chromatid.
D) haploid, and the chromosomes are each composed of two chromatids.
E) tetraploid, and the chromosomes are each composed of two chromatids.
D
How do cells at the completion of meiosis compare with cells that
have replicated their DNA and are just about to begin meiosis?
A) They have twice the amount of cytoplasm and half the amount of
DNA.
B) They have half the number of chromosomes and half the
amount of DNA.
C) They have the same number of chromosomes and half the amount of
DNA.
D) They have half the number of chromosomes and one-fourth
the amount of DNA.
E) They have half the amount of cytoplasm and twice the amount of DNA.
D
When does the synaptonemal complex disappear?
A) late prophase of meiosis I
B) during fertilization or
fusion of gametes
C) early anaphase of meiosis I
D) mid-prophase of meiosis II
E) late metaphase of meiosis II
A
Which of the following happens at the conclusion of meiosis I?
A) Homologous chromosomes of a pair are separated from each other.
B) The chromosome number per cell is conserved.
C) Sister
chromatids are separated.
D) Four daughter cells are
formed.
E) Cohesins are cleaved at the centromeres.
A
Chromatids are separated from each other.
A) The statement is
true for mitosis only.
B) The statement is true for meiosis I
only.
C) The statement is true for meiosis II only.
D) The
statement is true for mitosis and meiosis I.
E) The statement is true for mitosis and meiosis II.
E
Which of the following occurs in meiosis but not in mitosis?
A) chromosome replication
B) synapsis of chromosomes
C)
production of daughter cells
D) alignment of chromosomes at the equator E) condensation of chromatin
B
Whether during mitosis or meiosis, sister chromatids are held
together by proteins referred to as cohesins. Such molecules must have
which of the following properties?
A) They must persist
throughout the cell cycle.
B) They must be removed before
meiosis can begin.
C) They must be removed before sister chromatids or homologous chromosomes can separate.
D) They must reattach to chromosomes during G1.
E) They must
be intact for nuclear envelope re-formation.
C
Experiments with cohesins have found that
A) cohesins are
protected from destruction throughout meiosis I and II.
B)
cohesins are cleaved from chromosomes at the centromere before
anaphase I.
C) cohesins are protected from cleavage at the centromere during
meiosis I.
D) a protein cleaves cohesins before metaphase
I.
E) a protein that cleaves cohesins would cause cellular death.
C
A pair of homologous chromosomes includes which of the following sets
of DNA strands? A) two single-stranded chromosomes that have
synapsed
B) two sister chromatids that have synapsed
C)
four sister chromatids
D) four unique chromosomes
E) eight sister chromatids
B
When we see chiasmata under a microscope, that lets us know which of
the following has occurred?
A) asexual reproduction
B)
meiosis II
C) anaphase II
D) prophase I
E) separation of homologs
D
To visualize and identify meiotic cells at metaphase with a
microscope, what would you look for?
A) sister chromatids of a
replicated chromosome grouped at the poles
B) individual
chromosomes all at the cell's center
C) an uninterrupted spindle array
D) the synaptonemal
complex
E) pairs of homologous chromosomes all aligned at the
cell's center
E
For the following questions, match the key event of meiosis with the stages listed below.
- Prophase I
- Metaphase I
- Anaphase I
- Telophase I
V. Prophase II VI. Metaphase II VII. Anaphase II VIII. Telophase II
Centromeres of sister chromatids disjoin and chromatids separate.
A) II
B) III
C) IV
D) V
E) VII
E
For the following questions, match the key event of meiosis with the stages listed below.
- Prophase I
- Metaphase I
- Anaphase I
- Telophase I
V. Prophase II VI. Metaphase II VII. Anaphase II VIII. Telophase II
Homologous chromosomes are aligned at the equator of the spindle.
A) I
B) II
C) IV
D) VI
E) VIII
B
For the following questions, match the key event of meiosis with the stages listed below.
- Prophase I
- Metaphase I
- Anaphase I
- Telophase I
V. Prophase II VI. Metaphase II VII. Anaphase II VIII. Telophase II
Synaptonemal complexes form or are still present.
A) I only
B) I and IV only
C) I and VIII only
D) II and VI only
E) I, II, III, and IV only
A
The following question refers to the essential steps in meiosis described below.
1. Formation of four new nuclei, each with half the chromosomes
present in the parental nucleus 2. Alignment of homologous chromosomes
at the metaphase plate
3. Separation of sister chromatids
4. Separation of the homologs; no uncoupling of the centromere
5. Synapsis; chromosomes moving to the middle of the cell in pairs
Which of the steps take(s) place in both mitosis and meiosis?
A) 2
B) 3
C) 5
D) 2 and 3 only
E) 2, 3, and 5
B
For a species with a haploid number of 23 chromosomes, how many
different combinations of maternal and paternal chromosomes are
possible for the gametes?
A) 23
B) 46
C) 460
D) 920
E) about 8 million
E
Independent assortment of chromosomes is a result of
A) the
random and independent way in which each pair of homologous
chromosomes lines up at the metaphase plate during meiosis I.
B)
the random nature of the fertilization of ova by sperm.
C) the
random distribution of the sister chromatids to the two daughter cells
during anaphase II.
D) the relatively small degree of homology shared by the X and Y
chromosomes.
E) the random and independent way in which each
pair of homologous chromosomes lines up at the metaphase plate during
meiosis I, the random nature of the fertilization of ova by sperm, the
random distribution of the sister chromatids to the two daughter cells
during anaphase II, and the relatively small degree of homology shared
by the X and Y chromosomes.
A
Independent assortment of chromosomes occurs.
A) The statement is true for mitosis only.
B) The statement is
true for meiosis I only.
C) The statement is true for meiosis II only.
D) The statement is true for mitosis and meiosis I.
E) The statement is true for mitosis and meiosis II.
B
Which of the following best describes the frequency of crossing over in mammals?
A) ~50 per chromosome pair
B) ~2 per meiotic cell
C) at
least 1-2 per chromosome pair
D) ~1 per pair of sister chromatids
E) a very rare event among
hundreds of cells
C
When homologous chromosomes cross over, what occurs?
A) Two
chromatids get tangled, resulting in one re-sequencing its DNA.
B) Two sister chromatids exchange identical pieces of DNA.
C)
Specific proteins break the two strands of nonsister chromatids and
re-join them.
D) Each of the four DNA strands of a homologous
pair is broken, and the pieces are mixed.
E) Maternal alleles are "corrected" to be like paternal alleles, and vice versa.
C
In part III of Figure 10.1, the progression of events corresponds to
which of the following series?
A) zygote, mitosis, gametophyte,
mitosis, fertilization, zygote, mitosis
B) sporophyte, meiosis,
spore, mitosis, gametophyte, mitosis, gametes, fertilization
C) fertilization, mitosis, multicellular haploid, mitosis, spores, sporophyte
D) gametophyte, meiosis, zygote, spores, sporophyte, zygote
E)
meiosis, fertilization, zygote, mitosis, adult, meiosis
B
In a life cycle such as that shown in part III of Figure 10.1, if the
zygote's chromosome number is 10, which of the following will be
true?
A) The sporophyte's chromosome number per cell is 10 and
the gametophyte's is 5.
B) The sporophyte's chromosome number
per cell is 5 and the gametophyte's is 10.
C) The sporophyte and gametophyte each have 10 chromosomes per cell.
D) The sporophyte and gametophyte each have 5 chromosomes per cell.
E) The sporophyte and gametophyte each have 20 chromosomes per cell.
A
A certain female's number 12 chromosomes both have the blue gene and
number 19 chromosomes both have the long gene. As cells in her ovaries
undergo meiosis, her resulting eggs (ova) may have which of the
following?
A) either two number 12 chromosomes with blue genes
or two with orange genes
B) either two number 19 chromosomes with long genes or two with
short genes
C) either one blue or one orange gene in addition to
either one long or one short gene D) one chromosome 12 with one blue
gene and one chromosome 19 with one long gene
D
If a female of this species has one chromosome 12 with a blue gene
and another chromosome 12 with an orange gene, and has both number 19
chromosomes with short genes, she will produce which of the following
egg types?
A) only blue short gene eggs
B) only orange short gene eggs
C) one-half blue short and
one-half orange short gene eggs
D) three-fourths blue long and
one-fourth orange short gene eggs
E) three-fourths blue short and one-fourth orange short gene eggs
C
A female with a paternal set of one orange and one long gene
chromosome and a maternal set comprised of one blue and one short gene
chromosome is expected to produce which of the following types of eggs
after meiosis?
A) All eggs will have maternal types of gene combinations.
B) All eggs will have paternal types of gene combinations.
C)
Half the eggs will have maternal and half will have paternal
combinations.
D) Each egg has a one-fourth chance of having
either blue long, blue short, orange long, or orange short
combinations.
E) Each egg has a three-fourths chance of having
blue long, one-fourth blue short, three-fourths orange long, or
one-fourth orange short combinations.
D
Because the rotifers develop from eggs, but asexually, what can you predict?
A) The eggs and the zygotes are all haploid.
B) The animals
are all hermaphrodites.
C) Although asexual, both males and
females are found in nature.
D) All males can produce eggs.
E) No males can be found.
E
How is natural selection related to sexual reproduction as opposed to asexual reproduction?
A) Sexual reproduction results in many new gene combinations, some
of which will lead to differential reproduction.
B) Sexual
reproduction results in the most appropriate and healthiest balance of
two sexes in a population.
C) Sexual reproduction results in the greatest number of new
mutations.
D) Sexual reproduction allows the greatest number of
offspring to be produced.
E) Sexual reproduction utilizes far less energy than asexual reproduction.
A
A human cell containing 22 autosomes and a Y chromosome is
A) a sperm.
B) an egg.
C) a zygote.
D) a somatic cell of a male.
E) a somatic cell of a female.
A
Homologous chromosomes move toward opposite poles of a dividing cell during
A) mitosis.
B) meiosis I.
C) meiosis II.
D) fertilization.
E) binary fission
B
If the DNA content of a diploid cell in the G1 phase of the cell cycle is x, then the DNA content of the same cell at metaphase of meiosis I would be
A) 0.25x.
B) 0.5x.
C) x.
D) 2x.
E) 4x.
D
If we continued to follow the cell lineage from question 3, then the
DNA content of a single cell at metaphase of meiosis II would be
A) 0.25x.
B) 0.5x.
C) x.
D) 2x.
E) 4x
C
How many different combinations of maternal and paternal chromosomes
can be packaged in gametes made by an organism with a diploid number
of 8 (2n = 8)?
A) 2
B) 4
C) 8
D) 16
E) 32
D
What do we mean when we use the terms monohybrid cross and dihybrid
cross?
A) A monohybrid cross involves a single parent, whereas a
dihybrid cross involves two parents.
B) A monohybrid cross produces a single progeny, whereas a dihybrid
cross produces two progeny.
C) A dihybrid cross involves
organisms that are heterozygous for two characters, and a monohybrid
cross involves only one.
D) A monohybrid cross is performed for
one generation, whereas a dihybrid cross is performed for two
generations.
E) A monohybrid cross results in a 9:3:3:1 ratio,
whereas a dihybrid cross gives a 3:1 ratio.
C
What was the most significant conclusion that Gregor Mendel drew from
his experiments with pea plants?
A) There is considerable
genetic variation in garden peas.
B) Traits are inherited in
discrete units, and are not the results of "blending."
C) Recessive genes occur more frequently in the F1 generation than do dominant ones.
D) Genes are composed of DNA.
E) An organism that is homozygous for many recessive traits is at a disadvantage.
B
How many unique gametes could be produced through independent
assortment by an individual with the genotype AaBbCCDdEE?
A)
4
B) 8
C) 16
D) 32
E) 64
B
The individual with genotype AaBbCCDdEE can make many kinds of
gametes. Which of the following is the major reason?
A)
segregation of maternal and paternal alleles
B) recurrent
mutations forming new alleles
C) crossing over during prophase I
D) different possible
assortment of chromosomes into gametes
E) the tendency for dominant alleles to segregate together
D
Why did Mendel continue some of his experiments to the F2 or F3 generation?
A) to obtain a larger number of offspring on which to base statistics
B) to observe whether or not a recessive trait would reappear
C) to observe whether or not the dominant trait would reappear
D) to distinguish which alleles were segregating
E) to be able
to describe the frequency of recombination
B
Which of the following differentiates between independent assortment and segregation?
A) The law of independent assortment requires describing two or more
genes relative to one another.
B) The law of segregation
requires describing two or more genes relative to one another.
C) The law of segregation requires having two or more generations to
describe.
D) The law of independent assortment is accounted for
by observations of prophase I. E) The law of segregation is accounted
for by anaphase of mitosis.
A
Two plants are crossed, resulting in offspring with a 3:1 ratio for a
particular trait. What does this suggest?
A) that the parents
were true-breeding for contrasting traits
B) that the trait
shows incomplete dominance
C) that a blending of traits has occurred
D) that the parents
were both heterozygous for a single trait
E) that each offspring
has the same alleles for each of two traits
D
A sexually reproducing animal has two unlinked genes, one for head
shape (H) and one for tail length (T). Its genotype is HhTt. Which of
the following genotypes is possible in a gamete from this
organism?
A) tt
B) Hh
C) HhTt
D) T
E) HT
E
When crossing an organism that is homozygous recessive for a single
trait with a heterozygote, what is the chance of producing an
offspring with the homozygous recessive phenotype?
A) 0%
B) 25%
C) 50%
D) 75%
E) 100%
C
Mendel accounted for the observation that traits that had disappeared
in the F1 generation reappeared in the F2 generation by proposing
that
A) new mutations were frequently generated in the F2
progeny, "reinventing" traits that had been lost in the
F1.
B) the mechanism controlling the appearance of traits was
different between the F1 and the F2 plants.
C) traits can be
dominant or recessive, and the recessive traits were obscured by the
dominant ones in the F1.
D) the traits were lost in the F1 due
to dominance of the parental traits.
E) members of the F1
generation had only one allele for each trait, but members of the F2
had two alleles for each trait.
C
The fact that all seven of the pea plant traits studied by Mendel
obeyed the principle of independent assortment most probably indicates
which of the following?
A) None of the traits obeyed the law of
segregation.
B) The diploid number of chromosomes in the pea
plants was 7.
C) All of the genes controlling the traits were located on the same
chromosome.
D) All of the genes controlling the traits behaved
as if they were on different chromosomes.
E) The formation of gametes in plants occurs by mitosis only.
D
Mendel's observation of the segregation of alleles in gamete
formation has its basis in which of the following phases of cell
division?
A) prophase I of meiosis
B) anaphase II of meiosis
C) metaphase I of meiosis
D) anaphase I of meiosis
E) anaphase of mitosis
D
Mendel's second law of independent assortment has its basis in which
of the following events of meiosis I?
A) synapsis of homologous
chromosomes
B) crossing over
C) alignment of tetrads at the equator
D) separation of homologs at anaphase
E) separation of cells at telophase
C
Why did the F1 offspring of Mendel's classic pea cross always look like one of the two parental varieties?
A) No genes interacted to produce the parental phenotype.
B) Each allele affected phenotypic expression.
C) The traits
blended together during fertilization.
D) One allele was dominant.
E) Phenotype was not dependent on genotype.
D
Black fur in mice (B) is dominant to brown fur (b). Short tails (T)
are dominant to long tails (t). What fraction of the progeny of
crosses BbTt × BBtt will be expected to have black fur and long
tails?
A) 1/16
B) 3/16
C) 3/8
D) 1/2
E) 9/16
D
In certain plants, tall is dominant to short. If a heterozygous plant
is crossed with a homozygous tall plant, what is the probability that
the offspring will be short?
A) 1
B) 1/2
C) 1/4
D) 1/6
E) 0
E
In the cross AaBbCc × AaBbCc, what is the probability of producing the genotype AABBCC?
A) 1/4
B) 1/8
C) 1/16
D) 1/32
E) 1/64
E
Given the parents AABBCc × AabbCc, assume simple dominance for each
trait and independent assortment. What proportion of the progeny will
be expected to phenotypically resemble the first parent?
A) 1/4
B) 1/8
C) 3/4
D) 3/8
E) 1
C
Which of the following is the best statement of the use of the
addition rule of probability?
A) the probability that two or
more independent events will both occur
B) the probability that
two or more independent events will both occur in the offspring of one
set of parents
C) the probability that either one of two
independent events will occur
D) the probability of producing
two or more heterozygous offspring
E) the likelihood that a
trait is due to two or more meiotic events
C
Which of the following calculations require that you utilize the
addition rule?
A) Calculate the probability of black offspring
from the cross AaBb × AaBb, when B is the symbol for black.
B)
Calculate the probability of children with both cystic fibrosis and
polydactyly when parents are each heterozygous for both genes.
C) Calculate the probability of each of four children having cystic
fibrosis if the parents are both heterozygous.
D) Calculate the
probability of a child having either sickle-cell anemia or cystic
fibrosis if parents are each heterozygous for both.
E) Calculate
the probability of purple flower color in a plot of 50 plants seeded
from a self- fertilizing heterozygous parent plant.
D
Marfan syndrome in humans is caused by an abnormality of the connective tissue protein fibrillin. Patients are usually very tall and thin, with long spindly fingers, curvature of the spine, sometimes weakened arterial walls, and sometimes ocular problems, such as lens dislocation. Which of the following would you conclude about Marfan syndrome from this information?
A) It is recessive.
B) It is dominant.
C) It has a late
age of onset (> 60).
D) It is pleiotropic.
E) It is epistatic.
D
In cattle, roan coat color (mixed red and white hairs) occurs in the
heterozygous (Rr) offspring of red (RR) and white (rr) homozygotes.
Which of the following crosses would produce offspring in the ratio of
1 red:2 roan:1 white?
A) red × white
B) roan × roan
C) white × roan
D) red × roan
E)
The answer cannot be determined from the information provided.
B
Which of the following describes the ability of a single gene to have
multiple phenotypic effects?
A) incomplete dominance
B)
multiple alleles
C) pleiotropy
D) epistasis
C
Cystic fibrosis affects the lungs, the pancreas, the digestive
system, and other organs, resulting in symptoms ranging from breathing
difficulties to recurrent infections. Which of the following terms
best describes this?
A) incomplete dominance
B) multiple
alleles
C) pleiotropy
D) epistasis
E) codominance
C
Which of the following is an example of polygenic inheritance?
A) pink flowers in snapdragons
B) the ABO blood group in
humans
C) Huntington's disease in humans
D) white and purple flower color in peas
E) skin pigmentation in humans
E
Hydrangea plants of the same genotype are planted in a large flower
garden. Some of the plants produce blue flowers and others pink
flowers. This can be best explained by which of the following?
A) the knowledge that multiple alleles are involved
B) the allele for blue hydrangea being completely dominant
C) the alleles being codominant
D) the fact that a mutation
has occurred
E) environmental factors such as soil pH
E
Which of the following provides an example of epistasis?
A)
Recessive genotypes for each of two genes (aabb) result in an albino
corn snake.
B) The allele b17 produces a dominant phenotype,
although b1 through b16 do not.
C) In rabbits and many other
mammals, one genotype (ee) prevents any fur color from
developing.
D) In Drosophila (fruit flies), white eyes can be
due to an X-linked gene or to a combination of other genes.
E)
In cacti, there are several genes for the type of spines.
C
A scientist discovers a DNA-based test for one allele of a particular
gene. This and only this allele, if homozygous, produces an effect
that results in death at or about the time of birth. Of the following,
which is the best use of this discovery?
A) Screen all newborns
of an at-risk population.
B) Design a test for identifying heterozygous carriers of the allele.
C) Introduce a normal allele into deficient newborns.
D)
Follow the segregation of the allele during meiosis.
E) Test
school-age children for the disorder.
B
The frequency of heterozygosity for the sickle-cell anemia allele is
unusually high, presumably because this reduces the frequency of
malaria. Such a relationship is related to which of the
following?
A) Mendel's law of independent assortment
B)
Mendel's law of segregation
C) Darwin's explanation of natural
selection
D) Darwin's observations of competition
E) the
malarial parasite changing the allele
C
One of two major forms of a human condition called neurofibromatosis
(NF 1) is inherited as a dominant gene, although it may range from
mildly to very severely expressed. If a young child is the first in
her family to be diagnosed, which of the following is the best
explanation?
A) The mother carries the gene but does not express
it at all.
B) One of the parents has very mild expression of the gene.
C) The condition skipped a generation in the family.
D) The
child has a different allele of the gene than the parents.
B
In each generation of this family after generation I, the age at
diagnosis is significantly lower than would be found in nonfamilial
(sporadic) cases of this cancer (~63 years). What is the most likely
reason?
A) Members of this family know to be checked for colon
cancer early in life.
B) Hereditary (or familial) cases of this cancer typically occur at
earlier ages than do nonfamilial forms.
C) This is pure chance;
it would not be expected if you were to look at a different
family.
D) This cancer requires mutations in more than this one gene.
E) Affected members of this family are born with colon cancer, and it can be detected whenever they are first tested.
B
The affected woman in generation IV is thinking about her future and
asks her oncologist (cancer specialist) whether she can know whether
any or all of her children will have a high risk of the same cancer.
The doctor would be expected to advise which of the following?
I. genetic counseling
II. prenatal diagnosis when/if she becomes
pregnant
III. testing to see whether she has the allele
IV.testing to see whether her future spouse or partner has the
allele
A) I only
B) II only
C) I, II, and IV
only
D) I, II, and III only
E) III and IV only
C
Two true-breeding stocks of pea plants are crossed. One parent has red, axial flowers and the other has white, terminal flowers; all F1 individuals have red, axial flowers. The genes for flower color and location assort independently.
If 1,000 F2 offspring resulted from the cross, approximately how many of them would you expect to have red, terminal flowers?
A) 65
B) 190
C) 250
D) 565
E) 750
B
Two true-breeding stocks of pea plants are crossed. One parent has red, axial flowers and the other has white, terminal flowers; all F1 individuals have red, axial flowers. The genes for flower color and location assort independently.
Among the F2 offspring, what is the probability of plants with white
axial flowers? A) 9/16
B) 1/16
C) 3/16
D) 1/8
E) 1/4
C
Labrador retrievers are black, brown, or yellow. In a cross of a black female with a brown male, results can be either all black puppies, 1/2 black to 1/2 brown puppies, or 3/4 black to 1/4 yellow puppies.
These results indicate which of the following? A) Brown is dominant to black.
B) Black is dominant to brown and to yellow.
C) Yellow is
dominant to black.
D) There is incomplete dominance.
E) Epistasis is involved.
E
Labrador retrievers are black, brown, or yellow. In a cross of a black female with a brown male, results can be either all black puppies, 1/2 black to 1/2 brown puppies, or 3/4 black to 1/4 yellow puppies.
How many genes must be responsible for these coat colors in Labrador retrievers?
A) 1
B) 2
C) 3
D) 4
E) 5
B
Labrador retrievers are black, brown, or yellow. In a cross of a black female with a brown male, results can be either all black puppies, 1/2 black to 1/2 brown puppies, or 3/4 black to 1/4 yellow puppies.
In one type cross of black × black, the results were as follows:
9/16 black
4/16 yellow
3/16 brown
The genotype eebb must result in which of the following?
A) black
B) brown
C) yellow
D) a lethal result
E) white
C
Radish flowers may be red, purple, or white. A cross between a red-flowered plant and a white- flowered plant yields all-purple offspring. The part of the radish we eat may be oval or long, with long being the dominant trait.
If true-breeding red long radishes are crossed with true-breeding white oval radishes, the F1 will be expected to be which of the following?
A) red and long
B) red and oval
C) white and long
D) purple and long
E) purple and oval
D
Radish flowers may be red, purple, or white. A cross between a red-flowered plant and a white- flowered plant yields all-purple offspring. The part of the radish we eat may be oval or long, with long being the dominant trait.
In the F2 generation of the above cross, which of the following phenotypic ratios would be expected?
A) 9:3:3:1
B) 9:4:3
C) 1:1:1:1
D)
1:1:1:1:1:1
E) 6:3:3:2:1:1
E
Radish flowers may be red, purple, or white. A cross between a red-flowered plant and a white- flowered plant yields all-purple offspring. The part of the radish we eat may be oval or long, with long being the dominant trait.
The flower color trait in radishes is an example of which of the following?
A) a multiple allelic system
B) sex linkage
C) codominance
D) incomplete dominance
E) epistasis
D
Drosophila (fruit flies) usually have long wings (+), but mutations in two different genes can
result in bent wings (bt) or vestigial wings (vg).
If a homozygous bent wing fly is mated with a homozygous vestigial wing fly, which of the following offspring would you expect?
A) all +bt +vg heterozygotes
B) 1/2 bent and 1/2 vestigial flies
C) all homozygous + flies
D) 3/4 bent to 1/4 vestigial
ratio
E) 1/2 bent and vestigial to 1/2 normal
A
Drosophila (fruit flies) usually have long wings (+), but mutations in two different genes can
result in bent wings (bt) or vestigial wings (vg).
If flies that are heterozygous for both the bent wing gene and the
vestigial wing gene are mated, what is the probability of offspring
with bent wings only?
A) 1/8
B) 3/8
C) 1/4
D) 9/16
E) 3/16
E
A dwarf, red snapdragon is crossed with a plant homozygous for
tallness and white flowers. What are the genotype and phenotype of the
F1 individuals?
A) ttRr–dwarf and pink
B) ttrr–dwarf and white
C) TtRr–tall and red
D) TtRr–tall and pink
E) TTRR–tall and red
D
If snapdragons are heterozygous for height as well as for flower
color, a mating between them will result in what ratio?
A)
9:3:3:1
B) 6:3:3:2:1:1
C) 1:2:1
D) 27:9:9:9:3:3:3:1
E) 9:4:3
B
How many different types of gametes would be possible in this system?
A) 1
B) 2
C) 4
D) 8
E) 16
C
One fish of this type has alleles 1 and 3 (S1S3) and its mate has alleles 2 and 4 (S2S4). If each allele confers a unit of color darkness such that S1 has one unit, S2 has two units, and so on,
then what proportion of their offspring would be expected to have five units of color?
A) 1/4
B) 1/5
C) 1/8
D) 1/2
E) 0
D
Gene S controls the sharpness of spines in a type of cactus. Cactuses with the dominant allele, S, have sharp spines, whereas homozygous recessive ss cactuses have dull spines. At the same time, a second gene, N, determines whether or not cactuses have spines. Homozygous recessive nn cactuses have no spines at all.
The relationship between genes S and N is an example of
A) incomplete dominance.
B) epistasis.
C) complete dominance.
D) pleiotropy.
E) codominance.
B
A cross between a true-breeding sharp-spined cactus and a spineless cactus would produce
A) all sharp-spined progeny.
B) 50% sharp-spined, 50%
dull-spined progeny.
C) 25% sharp-spined, 50% dull-spined, 25%
spineless progeny.
D) all spineless progeny.
E) It is impossible to determine the
phenotypes of the progeny.
A
If doubly heterozygous SsNn cactuses were allowed to self-pollinate, the F2 would segregate in which of the following ratios?
A) 3 sharp-spined:1 spineless
B) 1 sharp-spined:2
dull-spined:1 spineless C) 1 sharp-spined:1 dull-spined:1 spineless D)
1 sharp-spined:1 dull-spined
E) 9 sharp-spined:3 dull-spined:4 spineless
E
A blue budgie is crossed with a white budgie. Which of the following
results is not possible? A) green offspring only
B) yellow
offspring only
C) blue offspring only
D) green and yellow offspring
E) a 9:3:3:1 ratio
D
Two blue budgies were crossed. Over the years, they produced 22
offspring, 5 of which were white. What are the most likely genotypes
for the two blue budgies?
A) yyBB and yyBB
B) yyBB and yyBb
C) yyBb and yyBb
D) yyBB and yybb
E) yyBb and yybb
C
Which of the following is a possible partial genotype for the son?
A) IBIB
B) IBIA
C) ii
D) IBi
E) IAIA
D
Which of the following is a possible genotype for the mother?
A) IAIA
B) IBIB
C) ii
D) IAi
E) IAIB
D
Which of the following is a possible phenotype for the father?
A) A negative
B) O negative
C) B positive
D) AB negative
E) impossible to determine
C
If both children are of blood type M, which of the following is possible?
A) Each parent is either M or MN.
B) Each parent must be type
M.
C) Both children are heterozygous for this gene.
D) Neither parent can have the N allele.
E) The MN blood group
is recessive to the ABO blood group.
A
One species of a small birdlike animal has an extremely variable tail length, an example of polygenic inheritance. Geneticists have come to realize that there are eight separate genes for tail length per haploid genome, with each gene having two alleles. One allele for each gene (a1, b1, and so on) increases the length by 1 cm, whereas the other allele (a2, b2, and so on) increases it by 0.5 cm. One bird was analyzed and found to have the following genotype: a1a1b2b2c1c2d1d2e2e2f1f2g1g1h1h2
What is the length of its tail?
A) 6 cm
B) 8 cm
C) 12 cm
D) 24 cm
E) 36 cm
C
One species of green plant, with frondlike leaves, a spine-coated
stem, and purple cup- shaped flowers, is found to be self-pollinating.
Which of the following is true of this species? A) The species must be
haploid.
B) Its reproduction is asexual.
C) All members of the species have the same genotype.
D) Some of the seeds would have true-breeding traits.
E) All of its dominant traits are most frequent.
D
If the environmental parameters, such as temperature, humidity,
atmosphere, sunlight, and so on, are mostly Earthlike, which of the
following do you expect of its types of leaves, stems, and
flowers?
A) The genes for them would have originated on Earth.
B) Genes for these traits would have a common ancestor with those
from Earth.
C) Such plants could be safely eaten by
humans.
D) Genotypes for these traits would be identical to
those of Earth plants with the same traits.
E) Phenotypes would be selected for or against by these environmental factors.
E
When Thomas Hunt Morgan crossed his red-eyed F1 generation flies to
each other, the F2 generation included both red- and white-eyed flies.
Remarkably, all the white-eyed flies were male. What was the
explanation for this result?
A) The gene involved is on the Y chromosome.
B) The gene involved is on the X chromosome.
C) The gene
involved is on an autosome, but only in males.
D) Other male-specific factors influence eye color in flies.
E) Other female-specific factors influence eye color in flies.
B
Which of the following is the meaning of the chromosome theory of
inheritance as expressed in the early 20th century?
A)
Individuals inherit particular chromosomes attached to genes.
B)
Mendelian genes are at specific loci on the chromosome and in turn
segregate during meiosis.
C) Homologous chromosomes give rise to some genes and crossover chromosomes to other genes.
D) No more than a single pair of chromosomes can be found in a healthy normal cell.
E) Natural selection acts on certain chromosome arrays rather than on genes.
B
Males are more often affected by sex-linked traits than females
because
A) male hormones such as testerone often alter the
affects of mutations on the X chromosome.
B) female hormones such as estrogen often compensate for the effects
of mutations on the X chromosome.
C) X chromosomes in males
generally have more mutations than X chromosomes in females.
D) males are hemizygous for the X chromosome.
E) mutations on
the Y chromosome often worsen the effects of X-linked mutations.
D
SRY is best described in which of the following ways?
A) a gene
present on the X chromosome that triggers female development
B)
an autosomal gene that is required for the expression of genes on the
Y chromosome
C) a gene region present on the Y chromosome that
triggers male development
D) an autosomal gene that is required
for the expression of genes on the X chromosome
E) a gene
required for development, and males or females lacking the gene do not
survive past early childhood
C
In cats, black fur color is caused by an X-linked allele; the other
allele at this locus causes orange color. The heterozygote is
tortoiseshell. What kinds of offspring would you expect from the cross
of a black female and an orange male?
A) tortoiseshell females;
tortoiseshell males
B) black females; orange males
C) orange females; orange
males
D) tortoiseshell females; black males
E) orange females; black males
D
Red-green color blindness is a sex-linked recessive trait in humans. Two people with normal color vision have a color-blind son. What are the genotypes of the parents?
A) XnXn and XnY
B) XnXn and XNY
C) XNXN and XnY
D) XNXN and XNY
E) XNXn and XNY
E
Cinnabar eyes is a sex-linked recessive characteristic in fruit flies. If a female having cinnabar eyes is crossed with a wild-type male, what percentage of the F1 males will have cinnabar eyes?
A) 0%
B) 25%
C) 50%
D) 75%
E) 100%
E
Normally, only female cats have the tortoiseshell phenotype
because
A) the males die during embryonic development.
B)
a male inherits only one allele of the X-linked gene controlling hair
color.
C) the Y chromosome has a gene blocking orange
coloration.
D) only males can have Barr bodies.
E)
multiple crossovers on the Y chromosome prevent orange pigment production.
B
Sex determination in mammals is due to the SRY region of the Y
chromosome. An abnormality of this region could allow which of the
following to have a male phenotype? A) Turner syndrome, 45, X
B)
translocation of SRY to an autosome of a 46, XX individual
C) a
person with an extra X chromosome
D) a person with one normal
and one shortened (deleted) X
E) Down syndrome, 46, XX
B
In humans, clear gender differentiation occurs not at fertilization,
but after the second month of gestation. What is the first event of
this differentiation?
A) formation of testosterone in male
embryos
B) formation of estrogens in female embryos
C) anatomical differentiation of a penis in male embryos
D)
activation of SRY in male embryos and masculinization of the gonads E)
activation of SRY in females and feminization of the gonads
D
Duchenne muscular dystrophy is a serious condition caused by a recessive allele of a gene on the human X chromosome. The patients have muscles that weaken over time because they have absent or decreased dystrophin, a muscle protein. They rarely live past their 20s. How likely is it for a woman to have this condition?
A) Women can never have this condition.
B) One-half of the
daughters of an affected man would have this condition.
C)
One-fourth of the daughters of an affected father and a carrier mother
could have this condition.
D) Very rarely: it is rare that an
affected male would mate with a carrier female.
E) Only if a
woman is XXX could she have this condition.
D
All female mammals have one active X chromosome per cell instead of
two. What causes this?
A) activation of the XIST gene on the X
chromosome that will become the Barr body
B) activation of the
BARR gene on one X chromosome, which then becomes inactive
C) crossing over between the XIST gene on one X chromosome and a
related gene on an autosome
D) inactivation of the XIST gene on
the X chromosome derived from the male parent
E) attachment of
methyl (CH3) groups to the X chromosome that will remain active
A
Which of the following statements is true of linkage?
A) The
closer two genes are on a chromosome, the lower the probability that a
crossover will occur between them.
B) The observed frequency of
recombination of two genes that are far apart from each other has a
maximum value of 100%.
C) All of the traits that Mendel
studied–seed color, pod shape, flower color, and others–are due to
genes linked on the same chromosome.
D) Linked genes are found
on different chromosomes.
E) Crossing over occurs during
prophase II of meiosis.
A
How would one explain a testcross involving F1 dihybrid flies in which more parental-type offspring than recombinant-type offspring are produced?
A) The two genes are closely linked on the same chromosome.
B) The two genes are linked but on different chromosomes.
C)
Recombination did not occur in the cell during meiosis.
D) The
testcross was improperly performed.
E) Both of the characters are controlled by more than one gene.
A
What does a frequency of recombination of 50% indicate?
A) The
two genes are likely to be located on different chromosomes.
B)
All of the offspring have combinations of traits that match one of the
two parents.
C) The genes are located on sex chromosomes.
D) Abnormal
meiosis has occurred.
E) Independent assortment is hindered.
A
Three genes (A, B, and C) at three loci are being mapped in a
particular species. Each gene has two alleles, one of which results in
a phenotype that is markedly different from the wild type. The unusual
allele of gene A is inherited with the unusual allele of gene B or C
about 50% of the time. However, the unusual alleles of genes B and C
are inherited together 14.4% of the time. Which of the following
describes what is happening?
A) The three genes are showing
independent assortment.
B) The three genes are linked.
C)
Gene A is linked but genes B and C are not.
D) Gene A is
assorting independently of genes B and C, which are linked.
E)
Gene A is located 14.4 map units from genes B and C.
D
What is one map unit equivalent to?
A) the physical distance
between two linked genes
B) 1% frequency of recombination
between two genes
C) 1 nanometer of distance between two
genes
D) the distance between a pair of homologous
chromosomes
E) the recombination frequency between two genes
assorting independently
B
Recombination between linked genes comes about for what reason?
A) Mutation on one homolog is different from that on the other
homolog.
B) Independent assortment sometimes fails because
Mendel had not calculated appropriately.
C) When genes are linked they always "travel" together at
anaphase.
D) Crossovers between these genes result in
chromosomal exchange.
E) Nonrecombinant chromosomes break and
then re-join with one another.
D
Why does recombination between linked genes continue to occur?
A) Recombination is a requirement for independent assortment.
B) Recombination must occur or genes will not assort independently.
C) New allele combinations are acted upon by natural selection.
D) The forces on the cell during meiosis II always result in recombination.
E) Without recombination there would be an insufficient number of gametes.
C
Map units on a linkage map cannot be relied upon to calculate
physical distances on a chromosome for which of the following
reasons?
A) The frequency of crossing over varies along the
length of the chromosome.
B) The relationship between
recombination frequency and map units is different in every individual.
C) Physical distances between genes change during the course of the cell cycle.
D) The gene order on the chromosomes is slightly different in every individual.
E) Linkage map distances are identical between males and females.
A
What is the reason that closely linked genes are typically inherited together?
A) The likelihood of a crossover event between these two genes is
low.
B) The number of genes in a cell is greater than the number
of chromosomes.
C) Chromosomes are unbreakable.
D) Alleles are paired together during meiosis.
E) Genes align
that way during metaphase I of meiosis.
A
Sturtevant provided genetic evidence for the existence of four pairs
of chromosomes in Drosophila in which of these ways?
A) There
are four major functional classes of genes in Drosophila.
B)
Drosophila genes cluster into four distinct groups of linked genes.
C) The overall number of genes in Drosophila is a multiple of four.
D) The entire Drosophila genome has approximately 400 map units.
E) Drosophila genes have, on average, four different alleles.
B
If cell X enters meiosis, and nondisjunction of one chromosome occurs
in one of its daughter cells during meiosis II, what will be the
result at the completion of meiosis?
A) All the gametes
descended from cell X will be diploid.
B) Half of the gametes
descended from cell X will be n + 1, and half will be n - 1.
C) One-fourth of the gametes descended from cell X will be n + 1,
1/4 will be n - 1, and 1/2 will be n.
D) There will be three
extra gametes.
E) Two of the four gametes descended from cell X
will be haploid, and two will be diploid.
C
One possible result of chromosomal breakage is for a fragment to join
a nonhomologous chromosome. What is this alteration called?
A)
deletion
B) transversion
C) inversion
D) translocation
E) duplication
D
A nonreciprocal crossover causes which of the following products?
A) deletion only
B) duplication only
C) nondisjunction
D) deletion and duplication
E) duplication and nondisjunction
D
Of the following human aneuploidies, which is the one that generally
has the most severe impact on the health of the individual?
A)
47, +21
B) 47, XXY
C) 47, XXX
D) 47, XYY
E) 45, X
A
A phenotypically normal prospective couple seeks genetic counseling
because the man knows that he has a translocation of a portion of his
chromosome 4 that has been exchanged with a portion of his chromosome
12. Although he is normal because his translocation is balanced, he
and his wife want to know the probability that his sperm will be
abnormal. What is your prognosis regarding his sperm?
A)
One-fourth will be normal, 1/4 will have the translocation, and 1/2
will have duplications and deletions.
B) All will carry the same
translocation as the father.
C) None will carry the
translocation because abnormal sperm will die.
D) His sperm will
be sterile and the couple might consider adoption.
E) One-half
will be normal and the rest will have the father's translocation.
A
Abnormal chromosomes are frequently found in malignant tumors. Errors
such as translocations may place a gene in close proximity to
different control regions. Which of the following might then occur to
make the cancer worse?
A) an increase in nondisjunction
B) expression of inappropriate gene products C) a decrease in
mitotic frequency
D) death of the cancer cells in the
tumor
E) sensitivity of the immune system
B
An inversion in a human chromosome often results in no demonstrable
phenotypic effect in the individual. What else may occur?
A)
There may be deletions later in life.
B) Some abnormal gametes
may be formed.
C) There is an increased frequency of mutation.
D) All inverted chromosomes are deleted.
E) The individual is
more likely to get cancer.
B
What is the source of the extra chromosome 21 in an individual with Down syndrome?
A) nondisjunction in the mother only
B) nondisjunction in the
father only
C) duplication of the chromosome
D) nondisjunction or translocation in either parent
E) It is impossible to detect with current technology.
D
Down syndrome has a frequency in the U.S. population of ~1/700 live
births. In which of the following groups would you expect this
frequency to be significantly higher?
A) people in Latin or
South America
B) the Inuit and other peoples in very cold habitats
C) people living in equatorial areas of the world
D) very small population groups
E) No groups have such higher frequency.
E
A couple has a child with Down syndrome. The mother is 39 years old
at the time of delivery. Which of the following is the most probable
cause of the child's condition?
A) The woman inherited this
tendency from her parents.
B) One member of the couple carried a translocation.
C) One member of the couple underwent nondisjunction in somatic cell production.
D) One member of the couple underwent nondisjunction in gamete
production.
E) The mother had a chromosomal duplication.
D
What is a syndrome?
A) a characteristic facial appearance
B) a group of traits, all of which must be present if an aneuploidy is
to be diagnosed
C) a group of traits typically found in
conjunction with a particular chromosomal aberration or gene
mutation
D) a characteristic trait usually given the
discoverer's name
E) a characteristic that only appears in
conjunction with one specific aneuploidy
C
Which of the following is known as a Philadelphia chromosome?
A) a human chromosome 22 that has had a specific translocation
B) a human chromosome 9 that is found only in one type of cancer
C) an animal chromosome found primarily in the mid-Atlantic area of
the United States
D) an imprinted chromosome that always comes from the mother
E) a chromosome found not in the nucleus but in mitochondria
A
At what point in cell division is a chromosome lost so that, after fertilization with a normal gamete, the result is an embryo with 45, X?
I. an error in anaphase I
II. an error in anaphase II
III. an error of the first postfertilization mitosis IV.an error in
pairing
A) I or II only
B) II or IV only
C) III or
IV only
D) I, II, or III only
E) I, II, III, or IV
E
Which of the following is true of aneuploidies in general?
A) A
monosomy is more frequent than a trisomy.
B) 45, X is the only
known human live-born monosomy.
C) Some human aneuploidies have
selective advantage in some environments.
D) Of all human
aneuploidies, only Down syndrome is associated with mental retardation.
E) An aneuploidy resulting in the deletion of a chromosome segment is less serious than a duplication.
B
A woman is found to have 47 chromosomes, including three X
chromosomes. Which of the following describes her expected
phenotype?
A) masculine characteristics such as facial
hair
B) enlarged genital structures
C) excessive emotional instability
D) healthy female of
slightly above-average height
E) sterile female
D
If recombination frequency is equal to distance in map units, what is
the approximate distance between genes A and B?
A) 1.5 map
units
B) 3 map units
C) 6 map units
D) 15 map units
E) 30 map units
B
What is the greatest benefit of having used a testcross for this
experiment?
A) The homozygous recessive parents are obvious to
the naked eye.
B) The homozygous parents are the only ones whose
crossovers make a difference. C) Progeny can be scored by their
phenotypes alone.
D) All of the progeny will be
heterozygous.
E) The homozygous recessive parents will be unable
to cross over.
C
How many of their daughters might be expected to be color-blind dwarfs?
A) all
B) none
C) half
D) one out of four
E) three out of four
B
What proportion of their sons would be color-blind and of normal height?
A) none
B) half
C) one out of four
D) three out of four
E) all
B
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) 25%
C) 50%
D) 75%
E) 100%
E
In his transformation experiments, what did Griffith observe?
A) Mutant mice were resistant to bacterial infections.
B) Mixing
a heat-killed pathogenic strain of bacteria with a living
nonpathogenic strain can convert some of the living cells into the
pathogenic form.
C) Mixing a heat-killed nonpathogenic strain of
bacteria with a living pathogenic strain makes the pathogenic strain
nonpathogenic.
D) Infecting mice with nonpathogenic strains of
bacteria makes them resistant to pathogenic strains.
E) Mice
infected with a pathogenic strain of bacteria can spread the infection
to other mice.
B
How do we describe transformation in bacteria?
A) the creation
of a strand of DNA from an RNA molecule
B) the creation of a strand of RNA from a DNA molecule
C) the infection of cells by a phage DNA molecule
D) the type
of semiconservative replication shown by DNA
E) assimilation of external DNA into a cell
E
After mixing a heat-killed, phosphorescent (light-emitting) strain of bacteria with a living, nonphosphorescent strain, you discover that some of the living cells are now phosphorescent. Which observation(s) would provide the best evidence that the ability to phosphoresce is a heritable trait?
A) DNA passed from the heat-killed strain to the living
strain.
B) Protein passed from the heat-killed strain to the
living strain.
C) The phosphorescence in the living strain is
especially bright.
D) Descendants of the living cells are also
phosphorescent.
E) Both DNA and protein passed from the
heat-killed strain to the living strain.
D
In trying to determine whether DNA or protein is the genetic
material, Hershey and Chase made use of which of the following
facts?
A) DNA contains sulfur, whereas protein does not.
B) DNA contains phosphorus, whereas protein does not.
C) DNA contains nitrogen, whereas protein does not.
D) DNA
contains purines, whereas protein includes pyrimidines.
E) RNA
includes ribose, whereas DNA includes deoxyribose sugars.
B
Which of the following investigators was (were) responsible for the
following discovery?
In DNA from any species, the amount of
adenine equals the amount of thymine, and the amount of guanine equals
the amount of cytosine.
A) Frederick Griffith
B) Alfred
Hershey and Martha Chase
C) Oswald Avery, Maclyn McCarty, and
Colin MacLeod
D) Erwin Chargaff
E) Matthew Meselson and
Franklin Stahl
D
Cytosine makes up 42% of the nucleotides in a sample of DNA from an organism. Approximately what percentage of the nucleotides in this sample will be thymine?
A) 8%
B) 16%
C) 31%
D) 42%
E) It cannot be determined from the
information provided.
A
Which of the following can be determined directly from X-ray
diffraction photographs of crystallized DNA?
A) the diameter of
the helix
B) the rate of replication
C) the sequence of nucleotides
D) the bond angles of the
subunits
E) the frequency of A vs. T nucleotides
A
It became apparent to Watson and Crick after completion of their model that the DNA molecule could carry a vast amount of hereditary information in which of the following?
A) sequence of bases
B) phosphate-sugar backbones
C) complementary pairing of bases
D) side groups of nitrogenous bases
E) different five-carbon sugars
A
In an analysis of the nucleotide composition of DNA, which of the
following will be found? A) A = C
B) A = G and C = T
C) A
+ C = G + T
D) G + C = T + A
C
What is meant by the description "antiparallel" regarding the strands that make up DNA?
A) The twisting nature of DNA creates nonparallel strands.
B)
The 5' to 3' direction of one strand runs counter to the 5' to 3'
direction of the other strand.
C) Base pairings create unequal spacing between the two DNA strands.
D) One strand is positively charged and the other is negatively
charged.
E) One strand contains only purines and the other
contains only pyrimidines.
B
Replication in prokaryotes differs from replication in eukaryotes for
which of the following reasons?
A) Prokaryotic chromosomes have
histones, whereas eukaryotic chromosomes do not.
B) Prokaryotic
chromosomes have a single origin of replication, whereas eukaryotic
chromosomes have many.
C) The rate of elongation during DNA replication is slower in prokaryotes than in eukaryotes.
D) Prokaryotes produce Okazaki fragments during DNA replication, but eukaryotes do not.
E) Prokaryotes have telomeres, and eukaryotes do not.
B
Suppose you are provided with an actively dividing culture of E. coli
bacteria to which radioactive thymine has been added. What would
happen if a cell replicates once in the presence of this radioactive
base?
A) One of the daughter cells, but not the other, would
have radioactive DNA.
B) Neither of the two daughter cells would
be radioactive.
C) All four bases of the DNA would be
radioactive.
D) Radioactive thymine would pair with
nonradioactive guanine.
E) DNA in both daughter cells would be radioactive.
E
An Okazaki fragment has which of the following arrangements?
A) primase, polymerase, ligase
B) 3' RNA nucleotides, DNA
nucleotides 5'
C) 5' RNA nucleotides, DNA nucleotides 3'
D) DNA polymerase I, DNA polymerase III
E) 5' DNA to 3'
C
In E. coli, there is a mutation in a gene called dnaB that alters the
helicase that normally acts at the origin. Which of the following
would you expect as a result of this mutation?
A) No
proofreading will occur.
B) No replication fork will be formed.
C) The DNA will supercoil.
D) Replication will occur via RNA
polymerase alone.
E) Replication will require a DNA template
from another source.
B
Which enzyme catalyzes the elongation of a DNA strand in the 5' → 3' direction?
A) primase
B) DNA ligase
C) DNA polymerase III
D) topoisomerase
E) helicase
C
At a specific area of a chromosome, the following sequence of
nucleotides is present where the chain opens to form a replication
fork:
3' C C T A G G C T G C A A T C C 5'
An RNA primer is
formed starting at the underlined T (T) of the template. Which of the
following represents the primer sequence?
A) 5' G C C T A G G 3'
B) 3' G C C T A G G 5'
C) 5' A C G T T A G G 3'
D) 5' A C G U U A G G 3'
E) 5' G C C U A G G 3'
D
Polytene chromosomes of Drosophila salivary glands each consist of
multiple identical DNA strands that are aligned in parallel arrays.
How could these arise?
A) replication followed by mitosis
B) replication without separation
C) meiosis followed by mitosis
D) fertilization by multiple
sperm
E) special association with histone proteins
B
To repair a thymine dimer by nucleotide excision repair, in which
order do the necessary enzymes act?
A) exonuclease, DNA
polymerase III, RNA primase
B) helicase, DNA polymerase I, DNA ligase
C) DNA ligase, nuclease, helicase
D) DNA polymerase I, DNA
polymerase III, DNA ligase
E) endonuclease, DNA polymerase I, DNA ligase
E
What is the function of DNA polymerase III?
A) to unwind the
DNA helix during replication
B) to seal together the broken ends
of DNA strands
C) to add nucleotides to the 3' end of a growing
DNA strand
D) to degrade damaged DNA molecules
E) to rejoin the two DNA strands (one new and one old) after replication
C
The difference between ATP and the nucleoside triphosphates used
during DNA synthesis is that
A) the nucleoside triphosphates
have the sugar deoxyribose; ATP has the sugar ribose.
B) the
nucleoside triphosphates have two phosphate groups; ATP has three
phosphate groups.
C) ATP contains three high-energy bonds; the nucleoside triphosphates have two.
D) ATP is found only in human cells; the nucleoside triphosphates
are found in all animal and plant cells.
E) triphosphate
monomers are active in the nucleoside triphosphates, but not in ATP.
A
The leading and the lagging strands differ in that
A) the
leading strand is synthesized in the same direction as the movement of
the replication fork, and the lagging strand is synthesized in the
opposite direction.
B) the leading strand is synthesized by
adding nucleotides to the 3' end of the growing strand, and the
lagging strand is synthesized by adding nucleotides to the 5'
end.
C) the lagging strand is synthesized continuously, whereas
the leading strand is synthesized in short fragments that are
ultimately stitched together.
D) the leading strand is
synthesized at twice the rate of the lagging strand.
A
A new DNA strand elongates only in the 5' to 3' direction
because
A) DNA polymerase begins adding nucleotides at the 5'
end of the template.
B) Okazaki fragments prevent elongation in
the 3' to 5' direction.
C) the polarity of the DNA molecule
prevents addition of nucleotides at the 3' end.
D) replication must progress toward the replication fork.
E)
DNA polymerase can only add nucleotides to the free 3' end.
E
What is the function of topoisomerase?
A) relieving strain in
the DNA ahead of the replication fork
B) elongating new DNA at a
replication fork by adding nucleotides to the existing chain
C) adding methyl groups to bases of DNA
D) unwinding of the
double helix
E) stabilizing single-stranded DNA at the
replication fork
A
What is the role of DNA ligase in the elongation of the lagging
strand during DNA replication?
A) It synthesizes RNA nucleotides
to make a primer.
B) It catalyzes the lengthening of telomeres.
C) It joins Okazaki fragments together.
D) It unwinds the
parental double helix.
E) It stabilizes the unwound parental DNA.
C
Which of the following help(s) to hold the DNA strands apart while
they are being replicated?
A) primase
B) ligase
C) DNA polymerase
D) single-strand binding proteins
E) exonuclease
D
Individuals with the disorder xeroderma pigmentosum are
hypersensitive to sunlight. This occurs because their cells are
impaired in what way?
A) They cannot replicate DNA.
B)
They cannot undergo mitosis.
C) They cannot exchange DNA with other cells.
D) They cannot
repair thymine dimers.
E) They do not recombine homologous
chromosomes during meiosis.
D
Use the list of choices below for the following questions:
- helicase
- DNA polymerase III
- ligase
- DNA polymerase I
- primase Which of the enzymes synthesizes short segments of RNA? A) I B) II C) III D) IV E) V
E
Use the list of choices below for the following questions:
- helicase
- DNA polymerase III
- ligase
- DNA polymerase I
- primase Which of the enzymes removes the RNA nucleotides from the primer and adds equivalent DNA nucleotides to the 3' end of Okazaki fragments? A) I B) II C) III D) IV E) V
D
Use the list of choices below for the following questions:
- helicase
- DNA polymerase III
- ligase
- DNA polymerase I
- primase Which of the enzymes separates the DNA strands during replication? A) I B) II C) III D) IV E) V
A
Use the list of choices below for the following questions:
- helicase
- DNA polymerase III
- ligase
- DNA polymerase I
- primase Which of the enzymes covalently connects segments of DNA? A) I B) II C) III D) IV E) V
C
Given the damage caused by UV radiation, the kind of gene affected in
those with XP is one whose product is involved with
A) mending
of double-strand breaks in the DNA backbone.
B) breakage of
cross-strand covalent bonds.
C) the ability to excise single-strand damage and replace it.
D) the removal of double-strand damaged areas.
E) causing
affected skin cells to undergo apoptosis.
C
Which of the following sets of materials is required by both
eukaryotes and prokaryotes for replication?
A) double-stranded
DNA, four kinds of dNTPs, primers, origins of replication
B)
topoisomerases, telomerases, polymerases
C) G-C rich regions, polymerases, chromosome nicks
D) nucleosome loosening, four dNTPs, four rNTPs
E) ligase, primers, nucleases
A
Studies of nucleosomes have shown that histones (except H1) exist in
each nucleosome as two kinds of tetramers: one of 2 H2A molecules and
2 H2B molecules, and the other as 2 H3 and 2 H4 molecules. Which of
the following is supported by this data?
A) DNA can wind itself
around either of the two kinds of tetramers.
B) The two types of
tetramers associate to form an octamer.
C) DNA has to associate
with individual histones before they form tetramers.
D) Only H2A
can form associations with DNA molecules.
E) The structure of H3
and H4 molecules is not basic like that of the other histones.
B
In a linear eukaryotic chromatin sample, which of the following
strands is looped into domains by scaffolding?
A) DNA without
attached histones
B) DNA with H1 only
C) the 10-nm chromatin fiber
D) the 30-nm chromatin fiber
E) the metaphase chromosome
D
Which of the following statements describes the eukaryotic
chromosome?
A) It is composed of DNA alone.
B) The
nucleosome is its most basic functional subunit.
C) The number
of genes on each chromosome is different in different cell types of an organism.
D) It consists of a single linear molecule of double-stranded DNA plus proteins.
E) Active transcription occurs on heterochromatin but not euchromatin.
D
If a cell were unable to produce histone proteins, which of the
following would be a likely effect?
A) There would be an
increase in the amount of "satellite" DNA produced during centrifugation.
B) The cell's DNA couldn't be packed into its nucleus.
C) Spindle fibers would not form during prophase.
D)
Amplification of other genes would compensate for the lack of
histones.
E) Pseudogenes would be transcribed to compensate for
the decreased protein in the cell.
B
Which of the following statements is true of histones?
A) Each
nucleosome consists of two molecules of histone H1.
B) Histone
H1 is not present in the nucleosome bead; instead, it draws the
nucleosomes together.
C) The carboxyl end of each histone extends outward from the
nucleosome and is called a "histone tail."
D) Histones
are found in mammals, but not in other animals or in plants or
fungi.
E) The mass of histone in chromatin is approximately nine
times the mass of DNA.
B
Why do histones bind tightly to DNA?
A) Histones are positively
charged, and DNA is negatively charged.
B) Histones are negatively charged, and DNA is positively charged.
C) Both histones and DNA are strongly hydrophobic.
D) Histones
are covalently linked to the DNA.
E) Histones are highly
hydrophobic, and DNA is hydrophilic.
A
Which of the following represents the order of increasingly higher
levels of organization of chromatin?
A) nucleosome, 30-nm
chromatin fiber, looped domain
B) looped domain, 30-nm chromatin
fiber, nucleosome
C) looped domain, nucleosome, 30-nm chromatin fiber
D) nucleosome, looped domain, 30-nm chromatin fiber
E) 30-nm chromatin fiber, nucleosome, looped domain
A
Which of the following statements describes chromatin?
A)
Heterochromatin is composed of DNA, whereas euchromatin is made of DNA
and RNA.
B) Both heterochromatin and euchromatin are found in the
cytoplasm.
C) Heterochromatin is highly condensed, whereas
euchromatin is less compact.
D) Euchromatin is not transcribed,
whereas heterochromatin is transcribed.
E) Only euchromatin is
visible under the light microscope.
C
Which of the following modifications is least likely to alter the
rate at which a DNA fragment moves through a gel during
electrophoresis?
A) altering the nucleotide sequence of the DNA
fragment without adding or removing nucleotides
B) acetylating the cytosine bases within the DNA fragment
C)
increasing the length of the DNA fragment
D) decreasing the
length of the DNA fragment
E) neutralizing the negative charges
within the DNA fragment
A
Assume that you are trying to insert a gene into a plasmid. Someone gives you a preparation of genomic DNA that has been cut with restriction enzyme X. The gene you wish to insert has sites on both ends for cutting by restriction enzyme Y. You have a plasmid with a single site for Y, but not for X. Your strategy should be to
A) insert the fragments cut with restriction enzyme X directly into
the plasmid without cutting the plasmid.
B) cut the plasmid with
restriction enzyme X and insert the fragments cut with restriction
enzyme Y into the plasmid.
C) cut the DNA again with restriction enzyme Y and insert these
fragments into the plasmid cut with the same enzyme.
D) cut the
plasmid twice with restriction enzyme Y and ligate the two fragments
onto the ends of the DNA fragments cut with restriction enzyme X.
E) cut the plasmid with restriction enzyme X and then insert the gene into the plasmid.
C
How does a bacterial cell protect its own DNA from restriction enzymes?
A) by adding methyl groups to adenines and cytosines
B) by using DNA ligase to seal the bacterial DNA into a closed
circle
C) by adding histones to protect the double-stranded DNA
D) by forming "sticky ends" of bacterial DNA to prevent the enzyme from attaching
E) by reinforcing the bacterial DNA structure with covalent phosphodiester bonds
A
What is the most logical sequence of steps for splicing foreign DNA into a plasmid and inserting the plasmid into a bacterium?
- Transform bacteria with a recombinant DNA molecule.
- Cut the plasmid DNA using restriction enzymes.
- Extract plasmid DNA from bacterial cells.
- Hydrogen-bond the plasmid DNA to nonplasmid DNA fragments.
- Use ligase to seal plasmid DNA to nonplasmid DNA.
A) I, II, IV, III, V
B) II, III, V, IV, I
C) III, II,
IV, V, I
D) III, IV, V, I, II
E) IV, V, I, II, III
C
Why is it so important to be able to amplify DNA fragments when studying genes?
A) DNA fragments are too small to use individually.
B) A gene
may represent only a millionth of the cell's DNA.
C) Restriction
enzymes cut DNA into fragments that are too small.
D) A clone requires multiple copies of each gene per clone.
E)
It is important to have multiple copies of DNA in the case of
laboratory error.
B
The reason for using Taq polymerase for PCR is that
A) it is
heat stable and can withstand the heating step of PCR.
B) only
minute amounts are needed for each cycle of PCR.
C) it binds
more readily than other polymerases to the primers.
D) it has
regions that are complementary to the primers.
E) it is heat
stable, and it binds more readily than other polymerases to the primers.
A
Once the pattern found after one round of replication was observed,
Meselson and Stahl could be confident of which of the following
conclusions?
A) Replication is semi-conservative.
B)
Replication is not dispersive.
C) Replication is not semi-conservative.
D) Replication is not
conservative.
E) Replication is neither dispersive nor conservative.
D
In an experiment, DNA is allowed to replicate in an environment with all necessary enzymes,
dATP, dCTP, dGTP, and radioactively labeled dTTP (3H thymidine). After several minutes, the DNA is switched to nonradioactive medium and is then viewed by electron microscopy and autoradiography. Figure 13.2 represents the results. It shows a replication bubble, and the dots represent radioactive material. Which of the following is the most likely interpretation of the results?
A) There are two replication forks going in opposite
directions.
B) Thymidine is being added only where the DNA
strands are farthest apart.
C) Thymidine is being added only at the very beginning of
replication.
D) Replication proceeds in one direction only.
A
Which enzyme was used to produce the molecule in Figure 13.3?
A) ligase
B) transcriptase
C) a restriction enzyme
D) RNA polymerase
E) DNA polymerase
C
For a science fair project, two students decided to repeat the Hershey and Chase experiment, with modifications. They decided to label the nitrogen of the DNA, rather than the phosphate. They reasoned that each nucleotide has only one phosphate and two to five nitrogens. Thus, labeling the nitrogens would provide a stronger signal than labeling the phosphates. Why won't this experiment work?
A) There is no radioactive isotope of nitrogen.
B) Radioactive
nitrogen has a half-life of 100,000 years, and the material would be
too dangerous for too long.
C) Avery et al. have already
concluded that this experiment showed inconclusive results.
D)
Although there are more nitrogens in a nucleotide, labeled phosphates
actually have 16 extra neutrons; therefore, they are more
radioactive.
E) Amino acids (and thus proteins) also have
nitrogen atoms; thus, the radioactivity would not distinguish between
DNA and proteins.
E
You briefly expose bacteria undergoing DNA replication to radioactively labeled nucleotides. When you centrifuge the DNA isolated from the bacteria, the DNA separates into two classes. One class of labeled DNA includes very large molecules (thousands or even millions of nucleotides long), and the other includes short stretches of DNA (several hundred to a few thousand nucleotides in length). These two classes of DNA probably represent
A) leading strands and Okazaki fragments.
B) lagging strands and Okazaki fragments.
C) Okazaki fragments and RNA primers.
D) leading strands and RNA primers.
E) RNA primers and mitochondrial DNA.
A
Bacteria that contain the plasmid, but not the eukaryotic gene, would
grow
A) in the nutrient broth plus ampicillin, but not in the
broth containing tetracycline.
B) only in the broth containing both antibiotics.
C) in the
broth containing tetracycline, but not in the broth containing ampicillin.
D) in all four types of broth.
E) in the nutrient broth
without antibiotics only.
D
Bacteria containing a plasmid into which the eukaryotic gene has
integrated would grow A) in the nutrient broth only.
B) in the
nutrient broth and the tetracycline broth only.
C) in the
nutrient broth, the ampicillin broth, and the tetracycline broth.
D) in all four types of broth.
E) in the ampicillin broth and
the nutrient broth.
E
Bacteria that do not take up any plasmids would grow on which media?
A) the nutrient broth only
B) the nutrient broth and the
tetracycline broth
C) the nutrient broth and the ampicillin broth
D) the tetracycline broth and the ampicillin broth
E) all three broths
A
Why might they be conducting such an experiment?
A) to find the
location of this gene in the human genome
B) to prepare to
isolate the chromosome on which the gene of interest is found
C) to find which of the students has which alleles
D) to
collect population data that can be used to assess natural
selection
E) to collect population data that can be used to
study genetic drift
C
Analysis of the data obtained shows that two students each have two fragments, two students each have three fragments, and two students each have one only. What does this demonstrate?
A) Each pair of students has a different gene for this
function.
B) The two students who have two fragments have one
restriction site in this region.
C) The two students who have two fragments have two restriction sites within this gene.
D) The students with three fragments are said to have "fragile
sites."
E) Each of these students is heterozygous for this gene.
B
In his work with pneumonia-causing bacteria and mice, Griffith found
that
A) the protein coat from pathogenic cells was able to
transform nonpathogenic cells.
B) heat-killed pathogenic cells
caused pneumonia.
C) some substance from pathogenic cells was
transferred to nonpathogenic cells, making them pathogenic.
D)
the polysaccharide coat of bacteria caused pneumonia.
E)
bacteriophages injected DNA into bacteria
C
What is the basis for the difference in how the leading and lagging
strands of DNA molecules are synthesized?
A) The origins of
replication occur only at the 5' end.
B) Helicases and
single-strand binding proteins work at the 5' end.
C) DNA polymerase can join new nucleotides only to the 3' end of a growing strand.
D) DNA ligase works only in the 3' → 5' direction.
E)
Polymerase can work on only one strand at a time.
C
In analyzing the number of different bases in a DNA sample, which
result would be consistent with the base-pairing rules?
A) A =
G
B) A + G = C + T
C) A + T = G + T
D) A = C
E) G = T
B
The elongation of the leading strand during DNA synthesis
A) progresses away from the replication fork.
B) occurs in the
3' → 5' direction.
C) produces Okazaki fragments.
D) depends on the action of DNA polymerase.
E) does not require a template strand.
D
In a nucleosome, the DNA is wrapped around A) polymerase
molecules.
B) ribosomes.
C) histones.
D) a thymine dimer.
E) satellite DNA.
C
E. coli cells grown on 15N medium are transferred to 14N medium and
allowed to grow for two more generations (two rounds of DNA
replication). DNA extracted from these cells is centrifuged. What
density distribution of DNA would you expect in this experiment?
A) one high-density and one low-density band
B) one intermediate-density band
C) one high-density and one
intermediate-density band
D) one low-density and one intermediate-density band
E) one low-density band
D
A biochemist isolates, purifies, and combines in a test tube a variety of molecules needed for DNA replication. When she adds some DNA to the mixture, replication occurs, but each DNA molecule consists of a normal strand paired with numerous segments of DNA a few hundred nucleotides long. What has she probably left out of the mixture?
A) DNA polymerase
B) DNA ligase
C) nucleotides
D) Okazaki fragments
E) primase
B
The spontaneous loss of amino groups from adenine in DNA results in hypoxanthine, an uncommon base, opposite thymine. What combination of proteins could repair such damage?
A) nuclease, DNA polymerase, DNA ligase
B) topoisomerase,
primase, DNA polymerase
C) topoisomerase, helicase, single-strand binding protein
D) DNA ligase, replication fork proteins, adenylyl cyclase
E) nuclease, topoisomerase, primase
A