Test Bank Karp8e CH9
Test Bank Karp8e CH9
Test Bank Karp8e CH9
1) Which type of cytoskeletal element is characterized as a hollow, rigid cylindrical tube with
walls composed of tubulin subunits?
a) microfilaments
b) microtubules
c) intermediate filaments
d) all of these choices
e) minitubules
Answer: b
Difficulty: Easy
Learning Objective: LO 9.1 Describe the components and major functions of the cytoskeleton.
Section Reference: Section 9.1 Overview of the Major Functions of the Cytoskeleton
a) microfilaments
b) microtubules
c) intermediate filaments
d) macrofilaments
e) indeterminate filaments
Answer: c
Difficulty: Easy
Learning Objective: LO 9.1 Describe the components and major functions of the cytoskeleton.
Section Reference: Section 9.1 Overview of the Major Functions of the Cytoskeleton
3) Which element of the cytoskeleton is found in the cytoplasm and the nucleus?
a) microfilaments
b) microtubules
c) intermediate filaments
d) macrofilaments
e) indeterminate filaments
Answer: c
Difficulty: Medium
Learning Objective: LO 9.1 Describe the components and major functions of the cytoskeleton.
Section Reference: Section 9.1 Overview of the Major Functions of the Cytoskeleton
4) Which cytoskeletal element is found could be described as solid, thinner structures that are
often organized into a branching network?
a) microfilaments
b) microtubules
c) intermediate filaments
d) macrotubules
e) minifilaments
Answer: a
Difficulty: Easy
Learning Objective: LO 9.1 Describe the components and major functions of the cytoskeleton.
Section Reference: Section 9.1 Overview of the Major Functions of the Cytoskeleton
5) You use an ionic detergent to extract materials from a cell. When you do, much of the mRNA
stays behind with the cytoskeleton, which is not solubilized by this treatment. What do these
results mean?
Answer: c
Difficulty: Hard
Learning Objective: LO 9.1 Describe the components and major functions of the cytoskeleton.
Section Reference: Section 9.1 Overview of the Major Functions of the Cytoskeleton
6) The splitting of the cytoplasm of a parent cell into two daughter cells is called ______.
a) diakinesis
b) cytokinesis
c) mitosis
d) meiosis
e) cytomegaly
Answer: b
Difficulty: Easy
Learning Objective: LO 9.1 Describe the components and major functions of the cytoskeleton.
Section Reference: Section 9.1 Overview of the Major Functions of the Cytoskeleton
Answer: c
Difficulty: Medium
Learning Objective: LO 9.4 Describe the experiments that support the hand-over-hand model of
action of kinesins.
Section Reference: Section 9.4 Experimental Pathway: The Step Size of Kinesin
a) provides structural support that determines cell shape and resists deforming forces
b) positions various organelles within the cell interior
c) provides a network of tracks over which materials like mRNA and organelles move within cells
d) serves as a force-generating apparatus that moves cells from one place to another
e) all of these choices
Answer: e
Difficulty: Medium
Learning Objective: LO 9.1 Describe the components and major functions of the cytoskeleton.
Section Reference: Section 9.1 Overview of the Major Functions of the Cytoskeleton
9) Which element of the cytoskeleton is found in the cytoplasm and the nucleus?
a) microfilaments
b) microtubules
c) intermediate filaments
d) macrofilaments
e) indeterminate filaments
Answer: c
Difficulty: Medium
Learning Objective: LO 9.1 Describe the components and major functions of the cytoskeleton.
Section Reference: Section 9.1 Overview of the Major Functions of the Cytoskeleton
a) intermediate filaments
b) microtubules
c) microfilaments
d) spindle fibers
e) microtubules and spindle fibers
Answer: a
Difficulty: Easy
Learning Objective: LO 9.1 Describe the components and major functions of the cytoskeleton.
Section Reference: Section 9.1 Overview of the Major Functions of the Cytoskeleton
11) In cell biology and with respect to microtubules, intermediate filaments, and microfilaments,
the word "dynamic" means ________.
a) impressive
b) constant
c) ever-changing
d) energetic
e) forceful
Answer: c
Difficulty: Easy
Learning Objective: LO 9.1 Describe the components and major functions of the cytoskeleton.
Section Reference: Section 9.1 Overview of the Major Functions of the Cytoskeleton
12) Which of the following could be a method used to label microtubules with a fluorescent dye?
Answer: e
Difficulty: Hard
Learning Objective: LO 9.2 Describe the structure and the functions of microtubules.
Section Reference: Section 9.2 Structure and Function of Microtubules
13) The microtubule wall is composed of globular proteins arranged in longitudinal rows called
_________.
a) microfilaments
b) protofilaments
c) prototubules
d) prototubulins
e) microtubular units
Answer: b
Difficulty: Medium
Learning Objective: LO 9.2 Describe the structure and the functions of microtubules.
Section Reference: Section 9.2 Structure and Function of Microtubules
14) In a normal microtubule, how many protofilaments make up its cylindrical wall?
a) 13
b) 15
c) 11
d) 9
e) 17
Answer: a
Difficulty: Easy
Learning Objective: LO 9.2 Describe the structure and the functions of microtubules.
Section Reference: Section 9.2 Structure and Function of Microtubules
15) What kinds of forces are thought to hold microtubular structure together?
a) strong interactions
b) noncovalent interactions
c) covalent interactions
d) magnetism
e) strong interactions and covalent interactions
Answer: b
Difficulty: Easy
Learning Objective: LO 9.2 Describe the structure and the functions of microtubules.
Section Reference: Section 9.2 Structure and Function of Microtubules
16) An abnormally high level of _______ of the MAP protein tau is implicated in the
development of strange, tangled filaments called _________ that have been seen in the brains of
patients suffering from several fatal neurodegenerative diseases like Alzheimer's disease.
Answer: a
Difficulty: Medium
Learning Objective: LO 9.2 Describe the structure and the functions of microtubules.
Section Reference: Section 9.2 Structure and Function of Microtubules
17) Given that axons growing out of a neuron require the growth outward of microtubules to
support the lengthening axon, what would be likely to happen to axons growing out from a
neuron when they are exposed to colchicine or nocodazole?
Answer: b
Difficulty: Medium
Learning Objective: LO 9.2 Describe the structure and the functions of microtubules.
Section Reference: Section 9.2 Structure and Function of Microtubules
a) Microtubules of the plant cell cortex are thought to affect the movement of cellulose-
synthesizing enzymes in the cell membrane, which, in turn, affect cell wall growth and shape.
b) Microtubules of the plant cell vacuole are thought to affect the movement of cellulose-
synthesizing enzymes in the cell membrane, which, in turn, affect cell wall growth and shape.
c) Microtubules of the plant cell cortex are thought to affect the movement of lipid-synthesizing
enzymes in the cell membrane, which, in turn, affect cell wall growth and shape.
d) Microtubules of the plant cell wall are thought to affect the movement of cellulose-
synthesizing enzymes in the cell membrane, which, in turn, affect cell wall growth and shape.
e) Microtubules of the plant cell nucleus are thought to affect the movement of cellulose-
synthesizing enzymes in the cell membrane, which, in turn, affect cell wall growth and shape.
Answer: a
Difficulty: Medium
Learning Objective: LO 9.2 Describe the structure and the functions of microtubules.
Section Reference: Section 9.2 Structure and Function of Microtubules
19) In a growing plant cell, cellulose microfibrils are oriented _______ the direction of cell
growth.
a) identically to
b) perpendicular to
c) parallel to
d) diagonal to
e) horizontal to
Answer: b
Difficulty: Easy
Learning Objective: LO 9.2 Describe the structure and the functions of microtubules.
Section Reference: Section 9.2 Structure and Function of Microtubules
20) In what form are proteins and neurotransmitters usually transported down the axon of a nerve
cell?
a) individually by diffusion
b) in groups of ten
c) inside transport vesicles
d) inside the Golgi complex
e) tied individually to microtubules
Answer: c
Difficulty: Medium
Learning Objective: LO 9.2 Describe the structure and the functions of microtubules.
Section Reference: Section 9.2 Structure and Function of Microtubules
21) Structures that move from the cell body of a neuron down the axon toward the neuron
terminals are said to move in a(n) _________ direction.
a) retrograde
b) anterograde
c) astronomical
d) radial
e) intergrade
Answer: b
Difficulty: Easy
Learning Objective: LO 9.2 Describe the structure and the functions of microtubules.
Section Reference: Section 9.2 Structure and Function of Microtubules
22) The movement of endocytic vesicles formed in the neuron terminals from the synapse to the
cell body is said to be in a(n) ________ direction.
a) retrograde
b) anterograde
c) astronomical
d) radial
e) intergrade
Answer: a
Difficulty: Easy
Learning Objective: LO 9.2 Describe the structure and the functions of microtubules.
Section Reference: Section 9.2 Structure and Function of Microtubules
a) kinesins
b) dyneins
c) myosins
d) kinesins and dyneins
c) kinesins and myosins
Answer: c
Difficulty: Easy
Learning Objective: LO 9.11 Explain how each type of myosin interacts with actin.
Section Reference: Section 9.3 Motor Proteins: Kinesins and Dyneins
24) Which of the following molecular motors is known to travel in a retrograde direction along
microtubules?
a) kinesins
b) dyneins
c) myosins
d) kinesins and myosins
e) kinesins and dyneins
Answer: b
Difficulty: Easy
Learning Objective: LO 9.3 Explain how kinesins and dyneins function as motor proteins within
a cell.
Section Reference: Section 9.3 Motor Proteins: Kinesins and Dyneins
25) Which of the following molecular motors is known to travel in an anterograde direction
along microtubules?
a) kinesins
b) dyneins
c) myosins
d) kinesins and dyneins
e) kinesins and myosins
Answer: a
Difficulty: Easy
Learning Objective: LO 9.3 Explain how kinesins and dyneins function as motor proteins within
a cell.
Section Reference: Section 9.3 Motor Proteins: Kinesins and Dyneins
26) What is the direct source of energy that powers molecular motors?
a) hydrolysis of GTP
b) hydrolysis of ATP
c) a proton gradient
d) a H+ gradient
e) condensation of ATP
Answer: b
Difficulty: Easy
Learning Objective: LO 9.3 Explain how kinesins and dyneins function as motor proteins within
a cell.
Section Reference: Section 9.3 Motor Proteins: Kinesins and Dyneins
27) What part of the molecular motor kinesin is responsible for binding to the cargo to be
hauled?
Answer: d
Difficulty: Easy
Learning Objective: LO 9.3 Explain how kinesins and dyneins function as motor proteins within
a cell.
Section Reference: Section 9.3 Motor Proteins: Kinesins and Dyneins
28) Kinesin movement along a microtubule is said to be highly ________ meaning that it can
move considerable distances along an individual microtubule without falling off.
a) excessive
b) processive
c) depressive
d) progressive
e) egressive
Answer: b
Difficulty: Easy
Learning Objective: LO 9.3 Explain how kinesins and dyneins function as motor proteins within
a cell.
Section Reference: Section 9.3 Motor Proteins: Kinesins and Dyneins
29) What is the minimum number of kinesin heads in contact with a microtubule at all times?
a) 0
b) 1
c) 2
d) 3
e) 4
Answer: b
Difficulty: Easy
Learning Objective: LO 9.3 Explain how kinesins and dyneins function as motor proteins within
a cell.
Section Reference: Section 9.3 Motor Proteins: Kinesins and Dyneins
Answer: a
Difficulty: Medium
Learning Objective: LO 9.3 Explain how kinesins and dyneins function as motor proteins within
a cell.
Section Reference: Section 9.4 Experimental Pathway: The Step Size of Kinesin
31) The simplest and the original assumption about step size for molecular motors was that as the
motor protein walked along the actin or microtubule polymer it would step__________.
a) 10 nm for every ATP that was hydrolyzed whether it was traveling along actin or tubulin
b) the distance of one tubulin dimer or actin subunit for every 2 ATPs that were hydrolyzed
c) the distance of three tubulin dimers or actin subunits for every ATP that was hydrolyzed
d) random distances along the cytoskeletal polymer for every ATP that was hydrolyzed
e) the distance of one tubulin dimer or actin subunit for every ATP that was hydrolyzed
Answer: e
Difficulty: Medium
Learning Objective: LO 9.4 Describe the experiments that support the hand-over-hand model of
action of kinesins.
Section Reference: Section 9.4 Experimental Pathway: The Step Size of Kinesin
32) The first direct measurement of a motor taking single steps was an analysis of _______
stepping using _________.
Answer: c
Difficulty: Medium
Learning Objective: LO 9.4 Describe the experiments that support the hand-over-hand model of
action of kinesins.
Section Reference: Section 9.4 Experimental Pathway: The Step Size of Kinesin
33) In order to measure the step size of kinesin, a group of investigators attached a small silica
bead to the tail of a kinesin molecule. What advantage(s) did the attached silica bead provide?
Answer: e
Difficulty: Medium
Learning Objective: LO 9.4 Describe the experiments that support the hand-over-hand model of
action of kinesins.
Section Reference: Section 9.4 Experimental Pathway: The Step Size of Kinesin
34) The current model for the nucleation of microtubules is that a helical array of -tubulin
subunits forms an open, lock-washer-like ring-shaped template upon which the first row of -
tubulin dimers assembles. How does this model account for the polarity of microtubules?
Answer: a
Difficulty: Medium
Learning Objective: LO 9.5 Describe microtubule organizing centers, their structures and
functions.
Section Reference: Section 9.5 Microtubule-Organizing Centers (MTOCs)
35) Nucleation of microtubules takes place rapidly inside a cell, where it occurs in association
with a variety of specialized structures called _____________.
a) MTOCs
b) the centrosome
c) basal bodies
d) microtubule-organizing centers
e) All of the other answers
Answer: e
Difficulty: Easy
Learning Objective: LO 9.5 Describe microtubule organizing centers, their structures and
functions.
Section Reference: Section 9.5 Microtubule-Organizing Centers (MTOCs)
Answer: a
Difficulty: Easy
Learning Objective: LO 9.5 Describe microtubule organizing centers, their structures and
functions.
Section Reference: Section 9.5 Microtubule-Organizing Centers (MTOCs)
a) a centrosome
b) basal bodies
c) centriole
d) PCM
e) the plus end
Answer: b
Difficulty: Easy
Learning Objective: LO 9.5 Describe microtubule organizing centers, their structures and
functions.
Section Reference: Section 9.5 Microtubule-Organizing Centers (MTOCs)
Answer: e
Difficulty: Easy
Learning Objective: LO 9.5 Describe microtubule organizing centers, their structures and
functions.
Section Reference: Section 9.5 Microtubule-Organizing Centers (MTOCs)
39) A small zone of fluorescent microtubules in a cell is photobleached so that their fluorescent
label gives off no light. Some time later fluorescence returns to the bleached zone in the cell.
Which of the following is a possible explanation for the recovery of fluorescence in the region of
the cell previously bleached?
a) the dynamics of the microtubules turning over in that bleached zone of the cell
b) the growth of new microtubules into the bleached zone
c) movement of microtubules through the bleached zone
d) all of these choices
e) the dynamics of the microtubules turning over in that bleached zone of the cell and the growth
of new microtubules into the bleached zone
Answer: d
Difficulty: Medium
Learning Objective: LO 9.6 Explain the underlying basis of microtubule dynamics.
Section Reference: Section 9.6 Microtubule Dynamics
40) Which of the following treatments does not disassemble microtubules in living cells?
Answer: a
Difficulty: Medium
Learning Objective: LO 9.6 Explain the underlying basis of microtubule dynamics.
Section Reference: Section 9.6 Microtubule Dynamics
41) Why are taxol, vinblastine and other drugs like them used as chemotherapy agents?
Answer: a
Difficulty: Medium
Learning Objective: LO 9.6 Explain the underlying basis of microtubule dynamics.
Section Reference: Section 9.6 Microtubule Dynamics
42) Which of the following treatments did not help microtubules to polymerize when
homogenates prepared from brain tissue received it?
a) Mg2+ ions
b) GTP
c) EGTA
d) a temperature of 37°C
e) a temperature of 4°C
Answer: e
Difficulty: Hard
Learning Objective: LO 9.6 Explain the underlying basis of microtubule dynamics.
Section Reference: Section 9.6 Microtubule Dynamics
43) Which of the following is a plausible explanation for the fact that the chemical EGTA blocks
microtubule disassembly?
a) EGTA binds to Ca2+ ions, which are known to induce microtubule depolymerization.
b) EGTA binds to Mg2+ ions, which are known to induce microtubule depolymerization.
c) EGTA binds to Ca2+ ions, which are known to induce microtubule polymerization.
d) EGTA destroys Ca2+ ions, which are known to inhibit microtubule polymerization.
e) EGTA destroys Mg2+ ions, which are known to inhibit microtubule polymerization.
Answer: a
Difficulty: Medium
Learning Objective: LO 9.6 Explain the underlying basis of microtubule dynamics.
Section Reference: Section 9.6 Microtubule Dynamics
44) To which end of microtubules are tubulin subunits primarily added in vitro?
Answer: c
Difficulty: Easy
Learning Objective: LO 9.6 Explain the underlying basis of microtubule dynamics.
Section Reference: Section 9.6 Microtubule Dynamics
Answer: d
Difficulty: Medium
Learning Objective: LO 9.7 Explain how the movement of cilia and flagella relates to their
structure and function.
Section Reference: Section 9.7 Structure and Function of Cilia and Flagella
Answer: d
Difficulty: Easy
Learning Objective: LO 9.7 Explain how the movement of cilia and flagella relates to their
structure and function.
Section Reference: Section 9.7 Structure and Function of Cilia and Flagella
47) Which of the following is normally associated with the cilia of organisms from protists to
mammals?
a) a 9 + 0 pattern
b) a 9 + 1 pattern
c) a 9 + 2 pattern
d) microtubules
e) none of these choices
Answer: c
Difficulty: Easy
Learning Objective: LO 9.7 Explain how the movement of cilia and flagella relates to their
structure and function.
Section Reference: Section 9.7 Structure and Function of Cilia and Flagella
48) Of what protein are the arms attached to the A microtubule of the axoneme composed?
a) tubulin
b) actin
c) dynein
d) keratin
e) myosin
Answer: c
Difficulty: Easy
Learning Objective: LO 9.7 Explain how the movement of cilia and flagella relates to their
structure and function.
Section Reference: Section 9.7 Structure and Function of Cilia and Flagella
a) centromeres
b) basal bodies
c) centrioles
d) spindle
e) MTOC
Answer: b
Difficulty: Easy
Learning Objective: LO 9.7 Explain how the movement of cilia and flagella relates to their
structure and function.
Section Reference: Section 9.7 Structure and Function of Cilia and Flagella
50) The peripheral doublets of the axoneme are connected to one another by a(n) ________
composed of an elastic protein-based linkage called the _______.
Answer: c
Difficulty: Medium
Learning Objective: LO 9.7 Explain how the movement of cilia and flagella relates to their
structure and function.
Section Reference: Section 9.7 Structure and Function of Cilia and Flagella
51) What protein is responsible for intraflagellar transport of IFT trains back toward the cell
body?
a) kinesin-II
b) myosin
c) cytoplasmic dynein
d) kinesin
e) cytoplasmic kinesin
Answer: c
Difficulty: Easy
Learning Objective: LO 9.7 Explain how the movement of cilia and flagella relates to their
structure and function.
Section Reference: Section 9.7 Structure and Function of Cilia and Flagella
52) Treatment of isolated sperm axonemes with 0.6 M NaCl has been shown to remove
selectively the outer arms from the A microtubules of the axoneme, leaving the inner arms in
place. What would be the most likely effect on the NaCl-treated axoneme when ATP was added
to the medium?
Answer: b
Difficulty: Hard
Learning Objective: LO 9.7 Explain how the movement of cilia and flagella relates to their
structure and function.
Section Reference: Section 9.7 Structure and Function of Cilia and Flagella
53) EDTA is a chemical that binds to and removes (chelates) divalent cations from solution.
Treatment of isolated axonemes with EDTA leads to the removal of the inner and outer arms
extending from the A microtubules of the axoneme. Which of the following statements wouls
appear to be true based on this information?
a) Potassium ions are required for dynein to bind to the A tubules of the axoneme.
b) Chlorine ions are required for dynein to bind to the A tubules of the axoneme.
c) Magnesium ions are required for dynein to bind to the A tubules of the axoneme.
d) Magnesium ions are required for tubulin to bind to the A tubules of the axoneme.
e) Sodium ions are required for tubulin to bind to the A tubules of the axoneme.
Answer: c
Difficulty: Medium
Learning Objective: LO 9.7 Explain how the movement of cilia and flagella relates to their
structure and function.
Section Reference: Section 9.7 Structure and Function of Cilia and Flagella
54) The _______ link is an elastic protein-based linkage that connects tubulin doublets in cilia
and flagellae. The resultant bridges play an important role in ciliary and flagellar movement by
limiting the extent that adjacent doublets can slide over one another. The resistance to sliding
provided by these bridges causes the axoneme to bend.
a) plectin
b) filamentin
c) nexin
d) vimentin
e) myosin
Answer: c
Difficulty: Easy
Learning Objective: LO 9.7 Explain how the movement of cilia and flagella relates to their
structure and function.
Section Reference: Section 9.7 Structure and Function of Cilia and Flagella
55) ___________ are recently discovered diseases that result from organelle dysfunction.
Specifically, each of these diseases is a set of seemingly unrelated disease symptoms that all
result from defects in cilia.
a) Flagellopathies
b) Cilioflagellar diseases
c) Ciliopathies
d) Ciliary diseases
e) Pathophysicilias
Answer: c
Difficulty: Easy
Learning Objective: LO 9.8 Give examples of how ciliopathies can have serious health
consequences.
Section Reference: Section 9.8 The Human Perspective: The Role of Cilia in Development and
Disease
56) For a long time, it was thought that cilia were unimportant or _________, despite their
presence on almost all cells. This idea arose because the cilia on most cells are non‐motile, and it
was assumed that motility was the key function of cilia.
a) flagellar
b) execrable
c) ciliopathic
d) vestigial
e) vestibular
Answer: d
Difficulty: Easy
Learning Objective: LO 9.8 Give examples of how ciliopathies can have serious health
consequences.
Section Reference: Section 9.8 The Human Perspective: The Role of Cilia in Development and
Disease
57) PC1 and PC2 form a complex in which PC2 serves as a(n) ____________.
Answer: b
Difficulty: Easy
Learning Objective: LO 9.8 Give examples of how ciliopathies can have serious health
consequences.
Section Reference: Section 9.8 The Human Perspective: The Role of Cilia in Development and
Disease
58) Bardet‐Biedl syndrome (BBS) is caused by mutations in any one of a number of genes that
affect protein trafficking into cilia. Persons afflicted with BBS exhibit a remarkable range of
abnormalities, like polydactyly, obesity, kidney disease, etc. These disparate symptoms are
thought to reflect the function of cilia ________________.
Answer: e
Difficulty: Medium
Learning Objective: LO 9.8 Give examples of how ciliopathies can have serious health
consequences.
Section Reference: Section 9.8 The Human Perspective: The Role of Cilia in Development and
Disease
59) One surprising symptom of that occurs in roughly half of patients who have non-motile cilia
is a complete reversal of the left-right asymmetry of the internal organs. This condition is called
_________.
a) misplaced organs
b) situs reversus
c) ambiorganismus
d) sinus inversus
e) situs inversus
Answer: e
Difficulty: Easy
Learning Objective: LO 9.8 Give examples of how ciliopathies can have serious health
consequences.
Section Reference: Section 9.8 The Human Perspective: The Role of Cilia in Development and
Disease
Answer: c
Difficulty: Easy
Learning Objective: LO 9.8 Give examples of how ciliopathies can have serious health
consequences.
Section Reference: Section 9.8 The Human Perspective: The Role of Cilia in Development and
Disease
61) Researchers worked with mouse embryos that had non‐motile cilia and used a pump to drive
an artificially created flow over their surface. When the flow was leftward directed, the mice
developed _____________.
Difficulty: Medium
Learning Objective: LO 9.8 Give examples of how ciliopathies can have serious health
consequences.
Section Reference: Section 9.8 The Human Perspective: The Role of Cilia in Development and
Disease
62) The cilia-driven flow in human and mouse embryos is detected by ___________.
a) renin
b) the Na+-K+ pump
c) polycystins
d) polyphenylin
e) cysteine
Answer: c
Difficulty: Easy
Learning Objective: LO 9.8 Give examples of how ciliopathies can have serious health
consequences.
Section Reference: Section 9.8 The Human Perspective: The Role of Cilia in Development and
Disease
63) The cross-bridges that hold intermediate filaments together are composed of _______.
a) filamentin
b) plectin
c) ascriptin
d) dynein
e) myosin
Answer: b
Difficulty: Easy
Learning Objective: LO 9.9 Describe the structure and functions of intermediate filaments.
Section Reference: Section 9.9 Intermediate Filaments
64) The central, rod-shaped domain of an intermediate filament is flanked on each side by
globular domains of variable size and sequence. What structure forms the core of the central,
rod-shaped domain?
a) alpha-helix
b) beta-pleated sheet
c) double helix
d) quaternary coil
e) coiled coil
Answer: a
Difficulty: Easy
Learning Objective: LO 9.9 Describe the structure and functions of intermediate filaments.
Section Reference: Section 9.9 Intermediate Filaments
a) elastic
b) highly resistant to shrinkage
c) springy
d) ability to absorb mechanical stresses applied by the extracellular environment
e) hyperflexible
Answer: d
Difficulty: Easy
Learning Objective: LO 9.9 Describe the structure and functions of intermediate filaments.
Section Reference: Section 9.9 Intermediate Filaments
66) You inject labeled keratin subunits into cultured skin cells. What happens a few minutes
later?
Answer: b
Difficulty: Hard
Learning Objective: LO 9.9 Describe the structure and functions of intermediate filaments.
Section Reference: Section 9.9 Intermediate Filaments
a) alpha-tubulin
b) beta-tubulin
c) actin
d) keratin
e) myosin
Answer: d
Difficulty: Easy
Learning Objective: LO 9.9 Describe the structure and functions of intermediate filaments.
Section Reference: Section 9.9 Intermediate Filaments
68) What seems to control the assembly and disassembly of intermediate filaments?
a) denaturation
b) sulfation
c) phosphorylation and dephosphorylation
d) hydrolysis
e) hydroxylation
Answer: c
Difficulty: Easy
Learning Objective: LO 9.9 Describe the structure and functions of intermediate filaments.
Section Reference: Section 9.9 Intermediate Filaments
69) With which of the following structures are intermediate filaments associated?
Answer: e
Difficulty: Medium
Learning Objective: LO 9.9 Describe the structure and functions of intermediate filaments.
Section Reference: Section 9.9 Intermediate Filaments
70) What kind of cells seems to rely mostly on microfilaments for long-distance transport of
cytoplasmic vesicles and organelles, probably due to the restricted microtubule distribution in
these cells?
a) red blood cells
b) white blood cells
c) plant cells
d) neurons
e) muscle cells
Answer: c
Difficulty: Easy
Learning Objective: LO 9.10 Explain the structure of actin and its function in cell motility.
Section Reference: Section 9.10 Actin
71) Which of the following words best describes the structure of an actin filament?
Answer: d
Difficulty: Easy
Learning Objective: LO 9.10 Explain the structure of actin and its function in cell motility.
Section Reference: Section 9.10 Actin
72) Which of the following does not describe the types of microfilament organization normally
seen in cells?
a) ordered arrays
b) highly branched networks
c) tightly anchored bundles
d) cylindrical conglomerations
e) all of these choices describe types of microfilament organization
Answer: d
Difficulty: Medium
Learning Objective: LO 9.10 Explain the structure of actin and its function in cell motility.
Section Reference: Section 9.10 Actin
73) What chemical below is known to bind to free actin monomers and block their incorporation
into the polymer?
a) cytochalasins
b) nocodazole
c) phalloidin
d) latrunculin
e) phalloidin and latrunculin
Answer: d
Difficulty: Medium
Learning Objective: LO 9.10 Explain the structure of actin and its function in cell motility.
Section Reference: Section 9.10 Actin
a) myoglobin
b) kinesin
c) myosin
d) dynein
e) myometrium
Answer: c
Difficulty: Easy
Learning Objective: LO 9.11 Explain how each type of myosin interacts with actin.
Section Reference: Section 9.11 Myosin: The Molecular Motor of Actin
75) From where does the energy to run myosin motors come?
a) GTP
b) ATP
c) proton gradient
d) CTP
e) creatine phosphate
Answer: b
Difficulty: Easy
Learning Objective: LO 9.11 Explain how each type of myosin interacts with actin.
Section Reference: Section 9.11 Myosin: The Molecular Motor of Actin
76) The myosin filament is characterized as a(n) _________ filament.
a) bipolar
b) unipolar
c) tripolar
d) parallel
e) orthogonal
Answer: a
Difficulty: Easy
Learning Objective: LO 9.11 Explain how each type of myosin interacts with actin.
Section Reference: Section 9.11 Myosin: The Molecular Motor of Actin
77) A culture of Dictyostelium slime mold is prepared in which the myosin II gene is deleted. In
which activity or activities below are these cells unable to participate?
Answer: c
Difficulty: Medium
Learning Objective: LO 9.11 Explain how each type of myosin interacts with actin.
Section Reference: Section 9.11 Myosin: The Molecular Motor of Actin
78) Why is myosin V able to take very large steps along a microfilament?
Answer: b
Difficulty: Easy
Learning Objective: LO 9.11 Explain how each type of myosin interacts with actin.
Section Reference: Section 9.11 Myosin: The Molecular Motor of Actin
79) Along which structure do membranous vesicles and organelles typically move long distances
in an animal cell?
a) mitochondria
b) microtubules
c) microfilaments
d) intermediate filaments
e) lysosomes
Answer: b
Difficulty: Medium
Learning Objective: LO 9.2 Describe the structure and the functions of microtubules.
Section Reference: Section 9.11 Myosin: The Molecular Motor of Actin
80) Along which structure do membranous vesicles and organelles typically engage in local
movement in the cell periphery of an animal cell?
a) mitochondria
b) microtubules
c) microfilaments
d) intermediate filaments
e) lysosomes
Answer: c
Difficulty: Medium
Learning Objective: LO 9.10 Explain the structure of actin and its function in cell motility.
Section Reference: Section 9.11 Myosin: The Molecular Motor of Actin
Answer: b
Difficulty: Medium
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
82) Myofibrils in a muscle cell are made up of a repeating linear array of contractile units called
________.
a) sarcocytes
b) blastomeres
c) myomeres
d) sarcomeres
e) myotubules
Answer: d
Difficulty: Easy
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
83) What is the name of the lightly staining areas at the outer edges of a sarcomere?
a) A bands
b) H zones
c) I bands
d) Z lines
e) M lines
Answer: c
Difficulty: Easy
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
84) What is the name of the densely staining area between the lightly staining areas at the outer
edges of a sarcomere?
a) A bands
b) H zones
c) I bands
d) Z lines
e) M lines
Answer: a
Difficulty: Easy
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
85) Which region of the sarcomere contains only actin thin filaments or microfilaments?
a) A bands
b) H zones
c) I bands
d) Z lines
e) M lines
Answer: c
Difficulty: Medium
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
86) Which region of the sarcomere represents the region of overlap between the two types of
filaments in the sarcomere?
a) A bands
b) the part of the A band on either side of the H zone
c) I bands
d) Z lines
e) the part of the H zone on either side of the A band
Answer: b
Difficulty: Medium
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
87) What accounts for the decrease in the length of an entire muscle?
Answer: a
Difficulty: Medium
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
Answer: b
Difficulty: Medium
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
89) Which of the following would be an accurate title for a movie about the mechanism of
muscle contraction?
a) Sliding Lamina
b) Shortening Filaments
c) Sliding Filaments
d) And Then There Were Two
e) Filaments At Large
Answer: c
Difficulty: Easy
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
90) What protein is thought to act like a "molecular ruler" by regulating the number of actin
monomers that are allowed to assemble into a thin filament?
a) troponin
b) myosin
c) nebulin
d) titin
e) tropomyosin
Answer: c
Difficulty: Easy
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
91) What is the name of the largest protein yet discovered? It extends from the M line in the
center of the sarcomere along the myosin filament and past the A band to terminate at the Z line.
a) troponin
b) myosin
c) actinin
d) titin
e) tropomyosin
Answer: d
Difficulty: Easy
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
92) Why does an actin thin filament manage to move continuously during a contraction cycle?
Answer: b
Difficulty: Medium
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
93) A(n) ________ motor, like muscle myosin (myosin II) and unlike myosin V, remains in
contact with its track, in this case the thin filament, for only a small portion, less than 5 percent,
of the overall cycle.
a) processive
b) nonprocessive
c) efficient
d) small
e) large
Answer: b
Difficulty: Easy
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
a) ATP
b) ADP
c) GTP
d) GDP
e) none of these choices
Answer: a
Difficulty: Medium
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
95) The point at which the neuron axon terminus and the muscle fiber make contact is called the
_________.
a) neuromuscular terminus
b) nerve exons
c) neural conjunctions
d) neuromuscular junction
e) neuromuscular conjunction
Answer: d
Difficulty: Medium
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
96) What blocks the myosin-binding sites on actin thin filaments in a stimulated sarcomere?
a) troponin
b) myosin itself
c) tropomyosin
d) titin
e) nothing
Answer: e
Difficulty: Easy
Learning Objective: LO 9.12 Describe the molecular components of muscle and how they
interact in contraction.
Section Reference: Section 9.12 Muscle Organization and Contraction
97) What is a major influence in determining the organization and behavior of actin filaments
inside cells?
a) actinin-binding proteins
b) tubulin
c) actin-binding proteins
d) dynein
e) actin-binding proteins and dynein
Answer: c
Difficulty: Medium
Learning Objective: LO 9.13 Describe the function of each category of actin-binding proteins.
Section Reference: Section 9.13 Actin-Binding Proteins
98) Proteins that accelerate the polymerization of actin filaments are called ________.
a) nucleons
b) nucleating proteins
c) monomer-sequestering proteins
d) end-blocking proteins
e) nucleons and nucleating proteins
Answer: b
Difficulty: Medium
Learning Objective: LO 9.13 Describe the function of each category of actin-binding proteins.
Section Reference: Section 9.13 Actin-Binding Proteins
99) ________ proteins share considerable sequence homology with actins and accelerate the
polymerization of actin filaments.
a) Actin-nucleating
b) Actin-racemase
c) Actin-related
d) Tubulin-related
e) Actin-rated
Answer: c
Difficulty: Easy
Learning Objective: LO 9.13 Describe the function of each category of actin-binding proteins.
Section Reference: Section 9.13 Actin-Binding Proteins
100) A shift in the concentration or activity of which type of proteins can cause a shift in the
equilibrium between actin monomers and polymers?
a) nucleating proteins
b) monomer-sequestering proteins
c) endolysins
d) capping proteins
e) all of these choices
Answer: b
Difficulty: Medium
Learning Objective: LO 9.13 Describe the function of each category of actin-binding proteins.
Section Reference: Section 9.13 Actin-Binding Proteins
101) _________ proteins are able to alter the three-dimensional organization of an actin filament
population.
a) Monomer-polymerizing
b) Cross-linking
c) Filament-severing
d) Actin-filament depolymerizing
e) End-blocking
Answer: b
Difficulty: Easy
Learning Objective: LO 9.13 Describe the function of each category of actin-binding proteins.
Section Reference: Section 9.13 Actin-Binding Proteins
102) Which type of actin-binding protein is known to decrease cytoplasmic viscosity by breaking
existing actin filaments into two or more pieces?
a) monomer-polymerizing proteins
b) cross-linking proteins
c) filament-severing proteins
d) actin-filament depolymerizing proteins
e) end-blocking proteins
Answer: c
Difficulty: Easy
Learning Objective: LO 9.13 Describe the function of each category of actin-binding proteins.
Section Reference: Section 9.13 Actin-Binding Proteins
103) Which of the following nonmuscle cell activities do not involve actin filaments often
working in concert with myosin motors?
a) cytokinesis
b) blood platelet activation
c) vesicle trafficking
d) red blood cells carrying oxygen
e) changes in cell shape
Answer: d
Difficulty: Medium
Learning Objective: LO 9.14 Explain the molecular mechanisms of cellular motility.
Section Reference: Section 9.14 Cellular Motility
104) As a fibroblast moves, its leading edge extends from the cell as a broad, flattened, veil-like
protrusion called a ________.
a) pseudopodium
b) lamella
c) lamellipodium
d) podium
e) extensor
Answer: c
Difficulty: Easy
Learning Objective: LO 9.14 Explain the molecular mechanisms of cellular motility.
Section Reference: Section 9.14 Cellular Motility
105) One of the WASP/WAVE family of proteins, specifically WASP, the founding member of
the family, is associated with what disease below?
a) hemophilia
b) Wiskott-Aldrich syndrome
c) lymphoma
d) lupus erythematosus
e) Wallace's syndrome
Answer: b
Difficulty: Easy
Learning Objective: LO 9.14 Explain the molecular mechanisms of cellular motility.
Section Reference: Section 9.14 Cellular Motility
106) If you were to fix a fish keratocyte and stain it with fluorescent antibodies for myosin II,
where would you see the myosin II?
Answer: c
107) The focal complexes that form near the leading edge of a motile cell exert traction force
through their associated __________ and then typically disassemble as the cell moves forward or
mature into larger, more contractile focal adhesions.
a) microtubules
b) keratin filaments
c) vinculin filaments
d) actin filaments
e) actinin filaments
Answer: d
Difficulty: Easy
Learning Objective: LO 9.14 Explain the molecular mechanisms of cellular motility.
Section Reference: Section 9.14 Cellular Motility
108) It was found that Listeria infection could be spread from one cell to its neighbors on a petri
dish even in the presence of extracellular antibiotic. This suggested that ___________.
a) bacteria were somehow unable to infect new cells directly from their previous host cell
b) bacteria were somehow able to infect new cells directly from their previous host cell
c) bacteria were able to destroy antibiotics
d) bacteria deactivated the extracellular antibiotic
e) bacteria produced antibodies against the antibiotic
Answer: b
Difficulty: Medium
Learning Objective: LO 9.15 Describe how study of Listeria helped researchers to understand
actin-based motility.
Section Reference: Section 9.15 Experimental Pathway: Studying Actin-Based Motility Without
Cells
109) It was found that Listeria infection could not be spread from one cell to its neighbors on a
petri dish in the presence of cytochalasin. This suggested that ___________.
Answer: a
Difficulty: Hard
Learning Objective: LO 9.15 Describe how study of Listeria helped researchers to understand
actin-based motility.
Section Reference: Section 9.15 Experimental Pathway: Studying Actin-Based Motility Without
Cells
110) Using a macrophage‐like cell line, researchers infected one set of petri dishes with wild‐
type Listeria , and, as a negative control, infected another set with a Listeria mutant that
was unable to enter cells. At specific time points, the cells were fixed and prepared for electron
microscopy. Two hours after infection, they observed that the wild‐type Listeria in the cytoplasm
were surrounded by ______________.
a) a cloud of tubulin
b) a cloud of actin
c) a cloud of keratin
d) a growth cone
e) comet tails of actin filaments
Answer: b
Difficulty: Medium
Learning Objective: LO 9.15 Describe how study of Listeria helped researchers to understand
actin-based motility.
Section Reference: Section 9.15 Experimental Pathway: Studying Actin-Based Motility Without
Cells
111) Using a macrophage‐like cell line, researchers infected one set of petri dishes with wild‐
type Listeria, and, as a negative control, infected another set with a Listeria mutant that was
unable to enter cells. At specific time points, the cells were fixed and prepared for electron
microscopy. Four hours after infection, they observed that many of the wild‐type Listeria in the
cytoplasm ______________.
Answer: d
Difficulty: Medium
Learning Objective: LO 9.15 Describe how study of Listeria helped researchers to understand
actin-based motility.
Section Reference: Section 9.15 Experimental Pathway: Studying Actin-Based Motility Without
Cells
Answer: e
Difficulty: Medium
Learning Objective: LO 9.14 Explain the molecular mechanisms of cellular motility.
Section Reference: Section 9.15 Experimental Pathway: Studying Actin-Based Motility Without
Cells
113) A researcher injected photoactivatable actin monomers into cells that had been infected
with Listeria and selected actin tails to study in more detail using fluorescence video
microscopy. She photoactivated fluorescent actin in a small region of the tail and observed that
the faster-moving bacteria had __________ and demonstrated that the rate of movement and the
length of the tail were _______________.
Answer: a
Difficulty: Medium
Learning Objective: LO 9.15 Describe how study of Listeria helped researchers to understand
actin-based motility.
Section Reference: Section 9.15 Experimental Pathway: Studying Actin-Based Motility Without
Cells
114) Expression of the ActA protein in previously non-motile strains of bacteria allowed for the
_______________ and ___________ characteristic of pathogenic strains.
Answer: c
Difficulty: Medium
Learning Objective: LO 9.15 Describe how study of Listeria helped researchers to understand
actin-based motility.
Section Reference: Section 9.15 Experimental Pathway: Studying Actin-Based Motility Without
Cells
115) Which protein below is not strictly required for Listeria motility within an infected cell?
a) actin
b) Arp2/3
c) cofilin
d) profilin
e) capping protein
Answer: d
Difficulty: Medium
Learning Objective: LO 9.15 Describe how study of Listeria helped researchers to understand
actin-based motility.
Section Reference: Section 9.15 Experimental Pathway: Studying Actin-Based Motility Without
Cells
116) The tip, or __________, of an elongating axon resembles a highly motile, crawling
fibroblast, unlike the bulk of the axon that shows little outward evidence of motile activity.
a) pointiliac
b) elongation cone
c) lamellipodial extension
d) growth cone
e) growth extension
Answer: d
Difficulty: Easy
Learning Objective: LO 9.14 Explain the molecular mechanisms of cellular motility.
Section Reference: Section 9.16 Actin-dependent Processes During Development
117) Which of the following traits is not seen upon close examination of a living growth cone of
an elongating axon?
Difficulty: Medium
Learning Objective: LO 9.14 Explain the molecular mechanisms of cellular motility.
Section Reference: Section 9.16 Actin-dependent Processes During Development
118) What purpose are actin filaments presumed to fulfill in the locomotor protrusions in the
peripheral domain of the growth cone?
a) They are thought to be responsible for the motile activities of the growth cone and its
protrusions.
b) They are presumed to provide support for the thin, elongating axon.
c) They are thought to locate certain membrane proteins properly in the plasma membrane.
d) They are thought to play an essential role in steering the growth cone in the appropriate
direction.
e) all of these choices
Answer: a
Difficulty: Medium
Learning Objective: LO 9.14 Explain the molecular mechanisms of cellular motility.
Section Reference: Section 9.16 Actin-dependent Processes During Development
119) Which of the following molecules is diffusible and serves as an attractant for axons
growing within the early embryo?
a) ephrin
b) netrin
c) integrin
d) axin
e) guidin
Answer: b
Difficulty: Easy
Learning Objective: LO 9.14 Explain the molecular mechanisms of cellular motility.
Section Reference: Section 9.16 Actin-dependent Processes During Development
120) Which of the following molecules is a non-diffusible, integral protein of the plasma
membrane that binds specifically to its receptor on the surface of the growth cone? This protein
acts as a neuronal guidance factor.
a) ephrin
b) netrin
c) integrin
d) axin
e) guidin
Answer: a
Difficulty: Easy
Learning Objective: LO 9.14 Explain the molecular mechanisms of cellular motility.
Section Reference: Section 9.16 Actin-dependent Processes During Development
121) Toward the end of gastrulation in vertebrates, the ectodermal cells situated along the
embryo's dorsal surface elongate and form a tall epithelial layer that is called the _________.
a) gastrula
b) neuroderm
c) neuralemma
d) blastoderm
e) neural plate
Answer: e
Difficulty: Easy
Learning Objective: LO 9.16 Explain the molecular basis of changes in cell shape.
Section Reference: Section 9.16 Actin-dependent Processes During Development
122) The elongation of the cells of the neural plate occurs when ___________ become oriented
with their long axes parallel to that of the cells.
a) microfilaments
b) myosin filaments
c) intermediate filaments
d) microtubules
e) titin
Answer: e
Difficulty: Easy
Learning Objective: LO 9.16 Explain the molecular basis of changes in cell shape.
Section Reference: Section 9.16 Actin-dependent Processes During Development
123) After they have elongated, the cells of the neural epithelium become constricted at one end,
causing them to become wedge shaped and leading the entire layer of cells to curve inward.
What causes this constriction?
a) contraction of microtubules in the cytoplasm just above the basal cell membrane
b) lengthening of microtubules in the cytoplasm just below the apical cell membrane
c) contraction of a band of microfilaments that assemble in the cortical region of the cells just
above the basal cell membrane
d) contraction of a band of microfilaments that assemble in the cortical region of the cells just
beneath the apical cell membrane
e) shortening of microtubules in the cytoplasm just below the apical cell membrane
Answer: d
Difficulty: Medium
Learning Objective: LO 9.16 Explain the molecular basis of changes in cell shape.
Section Reference: Section 9.16 Actin-dependent Processes During Development
124) What would happen if you cultured a frog embryo just after gastrulation in the presence of
cytochalasin?
a) The cells of the neural plate would elongate more than normal.
b) The cells of the neural plate would elongate much less than normal or not at all.
c) The cells of the neural plate elongate normally but do not become constricted as usually
happens.
d) The cells of the neural plate elongate normally but become more constricted than they usually
do.
e) The cells of the neural plate do not elongate and do not become constricted as they usually do.
Answer: c
Difficulty: Hard
Learning Objective: LO 9.16 Explain the molecular basis of changes in cell shape.
Section Reference: Section 9.16 Actin-dependent Processes During Development
125) What would happen if you cultured a frog embryo just after gastrulation in the presence of
colchicine?
a) The cells of the neural plate would elongate more than normal.
b) The cells of the neural plate would elongate much less than normal or not at all.
c) The cells of the neural plate elongate normally but do not become constricted as usually
happens.
d) The cells of the neural plate elongate normally but become more constricted than they usually
do.
e) The cells of the neural plate do not elongate and do not become constricted as they usually do.
Answer: b
Difficulty: Hard
Learning Objective: LO 9.16 Explain the molecular basis of changes in cell shape.
Section Reference: Section 9.16 Actin-dependent Processes During Development
126) The role of building the cytokinetic ring during cell division in prokaryotes is executed by
_________.
a) actin
b) tubulin
c) FtsZ
d) ParM
e) Crescentin
Answer: c
Difficulty: Medium
Learning Objective: LO 9.17 Describe the functions of each of the components of the bacterial
cytoskeleton.
Section Reference: Section 9.17 The Bacterial Cytoskeleton
127) The protein FtsZ acts in the bacterial cell analogously to the ______ cytoskeleton during
eukaryotic cytokinesis and is a(n) _________ homolog that is found in nearly all prokaryotic
cells.
a) actin, actin
b) actin, tubulin
c) tubulin, actin
d) actin, intermediate filament
e) tubulin, tubulin
Answer: b
Difficulty: Medium
Learning Objective: LO 9.17 Describe the functions of each of the components of the bacterial
cytoskeleton.
Section Reference: Section 9.17 The Bacterial Cytoskeleton
128) The protein ParM has been shown to play a role in plasmid segregation during bacterial cell
division analogous to the action of ___________ during mitosis and is structurally similar to
__________.
a) microfilaments, actin
b) microfilaments, tubulin
c) microtubules, tubulin
d) intermediate filaments, keratin
e) microtubules, actin
Answer: e
Difficulty: Medium
Learning Objective: LO 9.17 Describe the functions of each of the components of the bacterial
cytoskeleton.
Section Reference: Section 9.17 The Bacterial Cytoskeleton
129) The protein Crescentin (CreS) has been implicated in regulating the shape of some bacterial
cells and forms bundled filaments that give bacteria containing it a highly curved shape; it
resembles __________.
a) microfilaments
b) microtubules
c) titin
d) intermediate filaments
e) ParM
Answer: d
Difficulty: Medium
Learning Objective: LO 9.17 Describe the functions of each of the components of the bacterial
cytoskeleton.
Section Reference: Section 9.17 The Bacterial Cytoskeleton
130) The protein _________ has been implicated in regulating the shape of some bacterial cells;
it is expressed in rod-shaped and helical bacteria. It resembles __________in structure.
a) MreB, tubulin
b) MreB, actin
c) CreS, tubulin
d) CreS, actin
e) ParM, keratin
Answer: b
Difficulty: Medium
Learning Objective: LO 9.17 Describe the functions of each of the components of the bacterial
cytoskeleton.
Section Reference: Section 9.17 The Bacterial Cytoskeleton
131) The deletion of the mreB gene in Escherichia coli results in __________.
a) rod-shaped cells
b) crescent-shaped cells
c) spherical cells
d) spiral cells
e) cells that look like bunches of grapes
Answer: c
Difficulty: Medium
Learning Objective: LO 9.17 Describe the functions of each of the components of the bacterial
cytoskeleton.
Section Reference: Section 9.17 The Bacterial Cytoskeleton
132) The deletion of the creS gene in Caulobacter crescentus results in __________.
Answer: a
Difficulty: Medium
Learning Objective: LO 9.17 Describe the functions of each of the components of the bacterial
cytoskeleton.
Section Reference: Section 9.17 The Bacterial Cytoskeleton
133) How can the rate of movement generated by molecular motors be measured?
Answer:
Difficulty: Medium
Learning Objective: LO 9.4 Describe the experiments that support the hand-over-hand model of
action of kinesins.
Section Reference: Section 9.4 The Step Size of Kinesin
Solution: Such measurements of the rate of movement generated by molecular motors are called
in vitro motility assays These assays are performed by coating a coverslip with myosin or
kinesin, for example, adding either actin filaments or microtubules along with a source of ATP in
the buffer, and then imaging the coverslip under a microscope. Motor activity then results in the
actin or microtubule being translocated across the field of view at a speed equal to the speed at
which the motor is walking along the filament.
134) Why would the addition of an irreversibly binding ATP analog to an in vitro system for
monitoring dynein molecular motors stop motor function?
Answer:
Difficulty: Hard
Learning Objective: LO 9.3 Explain how kinesins and dyneins function as motor proteins within
a cell.
Section Reference: Section 9.3 Motor Proteins: Kinesins and Dyneins
Solution: Such an ATP analog would bind to the molecular motor, but it would not be
hydrolyzed or released. This would paralyze further movement of the motor since the cycle of
conformational changes could not be completed.
135) An element of the cytoskeleton is treated with ferritin-labeled antibodies to dynein and
visualized in the electron microscope. Ferritin can be seen attached to these elements. What are
they? What physical property of the cytoskeletal element would support your conclusion?
Answer:
Difficulty: Medium
Learning Objective: LO 9.7 Explain how the movement of cilia and flagella relates to their
structure and function.
Section Reference: Section 9.7 Structure and Function of Cilia and Flagella
Solution: They are microtubules since dynein, a molecular motor identified with microtubules, is
part of the structure. If the element were hollow and the right diameter, this conclusion would be
supported.
136) A scientist observes the motion of a certain type of vesicle around the cell. She notices that
vesicle movement ceases when colchicine is added to the culture medium. What conclusion can
she draw?
Answer:
Difficulty: Medium
Learning Objective: LO 9.2 Describe the structure and the functions of microtubules.
Section Reference: Section 9.2 Structure and Function of Microtubules
Solution: Since colchicine inhibits microtubule function, it is likely that the vesicular movement
is orchestrated by microtubules.