Unit 3: Cytoskeleton and Nucleus - Practice Quiz

BTS118 — Cell Biology 60 Questions
0 Correct 0 Wrong 60 Left
0/60

1 What is the basic protein subunit of a microtubule?

Structure and functions of Microtubules Easy
A. Actin
B. Keratin
C. Myosin
D. Tubulin

2 Which cellular structure is commonly organized by microtubules?

Structure and functions of Microtubules Easy
A. Nucleoli
B. Ribosomes
C. Centrosomes
D. Lysosomes

3 Which motor protein generally moves cargo toward the plus end of a microtubule?

Structure and functions of Microtubules Easy
A. Kinesin
B. Dynein
C. Myosin
D. Collagen

4 What is one important function of microtubules during cell division?

Structure and functions of Microtubules Easy
A. Separating chromosomes
B. Producing ribosomal RNA
C. Forming the cleavage furrow
D. Digesting cellular waste

5 Which cytoskeletal filament is usually the thinnest?

Intermediate filaments and Actin Filaments Easy
A. Actin filament
B. Intermediate filament
C. Microtubule
D. Nuclear lamina

6 What is a major function of intermediate filaments?

Intermediate filaments and Actin Filaments Easy
A. Copying DNA
B. Making ATP
C. Digesting proteins
D. Providing tensile strength

7 Which protein is the main component of actin filaments?

Intermediate filaments and Actin Filaments Easy
A. Tubulin
B. Keratin
C. Actin
D. Lamin

8 Which motor protein interacts directly with actin filaments?

Intermediate filaments and Actin Filaments Easy
A. Dynein
B. Kinesin
C. Myosin
D. Lamin

9 Actin filaments are especially important in which process?

Intermediate filaments and Actin Filaments Easy
A. Ribosome production
B. DNA replication
C. Cell crawling
D. Nuclear pore assembly

10 How many membranes make up the nuclear envelope?

Nuclear Envelope- structure of nuclear pore complex Easy
A. Two membranes
B. Three membranes
C. Four membranes
D. One membrane

11 What is the main function of a nuclear pore complex?

Nuclear Envelope- structure of nuclear pore complex Easy
A. Digesting proteins
B. Building microtubules
C. Making ATP
D. Controlling nuclear transport

12 Nuclear pore complexes are embedded in which structure?

Nuclear Envelope- structure of nuclear pore complex Easy
A. Plasma membrane
B. Mitochondrial matrix
C. Nuclear envelope
D. Golgi membrane

13 What is the central passageway of a nuclear pore complex used for?

Nuclear Envelope- structure of nuclear pore complex Easy
A. Moving materials across the envelope
B. Breaking down glucose
C. Producing membrane lipids
D. Storing chromosomes

14 The nuclear lamina is located mainly on which side of the nuclear envelope?

Nuclear lamina Easy
A. Inside the inner nuclear membrane
B. Inside the nucleolus
C. Outside the plasma membrane
D. Within the mitochondrial membrane

15 Which proteins form the main structural network of the nuclear lamina?

Nuclear lamina Easy
A. Histones
B. Lamins
C. Myosins
D. Tubulins

16 What is one function of the nuclear lamina?

Nuclear lamina Easy
A. Supporting nuclear shape
B. Translating messenger RNA
C. Digesting damaged organelles
D. Producing cytoplasmic ATP

17 What signal directs many proteins into the nucleus?

Protein import and export through Nuclear pore complex Easy
A. Peroxisomal targeting signal
B. Nuclear localization signal
C. Signal peptide
D. Mitochondrial targeting signal

18 Which transport receptor commonly carries proteins into the nucleus?

Protein import and export through Nuclear pore complex Easy
A. Ribosome
B. Exportin
C. Lamin
D. Importin

19 What signal is commonly required for nuclear protein export?

Protein import and export through Nuclear pore complex Easy
A. Nuclear localization signal
B. Membrane anchor
C. Lysosomal signal
D. Nuclear export signal

20 Which small GTPase helps provide directionality for nuclear transport?

Regulation of Nuclear protein import and export Easy
A. Ras
B. Rho
C. Ran
D. Rab

21 A drug prevents tubulin subunits from adding to microtubule plus ends. Which cellular process would be most directly impaired?

Structure and functions of Microtubules Medium
A. Contraction of the actomyosin cortex
B. Assembly of desmosomal junctions
C. Formation of the nuclear lamina
D. Chromosome movement during mitosis

22 A cell treated with a compound that prevents GTP hydrolysis in tubulin would most likely show which effect?

Structure and functions of Microtubules Medium
A. Faster intermediate-filament turnover
B. More stable microtubules
C. Loss of nuclear pore complexes
D. Reduced actin filament branching

23 A motor protein moves cargo toward the microtubule-organizing center in an axon. Which motor is most likely responsible?

Structure and functions of Microtubules Medium
A. Myosin moving toward the minus end
B. Dynein moving toward the minus end
C. Kinesin moving toward the plus end
D. Myosin moving toward the plus end

24 If centrosome function is disrupted in a dividing animal cell, which defect is most likely?

Structure and functions of Microtubules Medium
A. Failure to anchor keratin filaments
B. Failure to polymerize actin at the cortex
C. Failure to organize spindle microtubules
D. Failure to synthesize nuclear pores

25 A mutation weakens keratin filament connections between epithelial cells. Which tissue-level consequence is most likely?

Intermediate filaments and Actin Filaments Medium
A. Increased susceptibility to tissue tearing
B. Reduced vesicle movement along axons
C. Faster chromosome segregation
D. Greater resistance to mechanical stress

26 A migrating cell cannot form branched actin networks at its leading edge. Which process would be most directly affected?

Intermediate filaments and Actin Filaments Medium
A. Transport of proteins through nuclear pores
B. Extension of lamellipodia
C. Assembly of the nuclear lamina
D. Attachment of chromosomes to spindle fibers

27 A toxin prevents actin filament depolymerization but does not block polymerization. What is the likely cellular outcome?

Intermediate filaments and Actin Filaments Medium
A. Permanent opening of nuclear pores
B. Complete loss of intermediate filaments
C. Rapid breakdown of microtubules
D. Excessively stable actin structures

28 A cell has normal actin polymerization but defective myosin II activity. Which event would be most impaired?

Intermediate filaments and Actin Filaments Medium
A. Assembly of nuclear pore subunits
B. Formation of the contractile ring
C. Maintenance of nuclear lamina structure
D. Transport toward microtubule minus ends

29 Which feature best explains why intermediate filaments are especially useful for resisting mechanical stress?

Intermediate filaments and Actin Filaments Medium
A. They hydrolyze ATP during contraction
B. They organize chromosomes at kinetochores
C. They form strong, flexible cable-like networks
D. They undergo rapid treadmilling

30 A mutation removes a nucleoporin that forms part of the central transport channel. Which consequence is most likely?

Nuclear Envelope- structure of nuclear pore complex Medium
A. Actin filaments cannot bind myosin
B. Microtubules lose their polarity
C. Intermediate filaments become phosphorylated
D. Selective nuclear transport becomes defective

31 Why can small ions pass through nuclear pore complexes more freely than large protein complexes?

Nuclear Envelope- structure of nuclear pore complex Medium
A. Small molecules contain nuclear localization signals, whereas large cargo lacks them
B. Small molecules are actively transported by dynein through the pore
C. Large cargo crosses through the nuclear membrane, whereas ions use pores
D. Small molecules diffuse through the pore, whereas larger cargo requires transport receptors

32 A defect prevents nuclear pore complexes from being inserted into the double membrane of the nuclear envelope. Which structure would be directly affected?

Nuclear Envelope- structure of nuclear pore complex Medium
A. Formation of desmosomal intermediate filaments
B. Polymerization of cytoplasmic actin
C. Exchange between nucleoplasm and cytoplasm
D. Attachment of ribosomes to rough endoplasmic reticulum

33 A mutation reduces lamin filament assembly. Which nuclear defect would be most likely?

Nuclear lamina Medium
A. Loss of actin filament polarity
B. Enhanced import of all cytosolic proteins
C. Increased nuclear-envelope fragility
D. Failure of mitochondrial protein synthesis

34 During mitosis, phosphorylation of nuclear lamins promotes which event?

Nuclear lamina Medium
A. Activation of actin-based muscle contraction
B. Assembly of cytoplasmic intermediate filaments
C. Permanent closure of nuclear pores
D. Disassembly of the nuclear lamina

35 A cell expresses a lamin variant that cannot be properly modified after translation. Which process may be disrupted during cell division?

Nuclear lamina Medium
A. Polymerization of tubulin at axon terminals
B. Formation of actin branches at the leading edge
C. Reassembly of the nuclear envelope
D. Movement of vesicles along intermediate filaments

36 A protein containing a functional nuclear localization signal is synthesized in the cytoplasm. Which factor typically recognizes this signal?

Protein import and export through Nuclear pore complex Medium
A. Exportin
B. Kinesin
C. Importin
D. A lamin-associated protein

37 A nuclear protein remains in the cytoplasm even though its nuclear localization signal is intact. A mutation in which factor could explain this result?

Protein import and export through Nuclear pore complex Medium
A. Cytoplasmic importin
B. Intermediate-filament cross-linker
C. Actin nucleator
D. Nuclear exportin

38 A newly synthesized RNA-binding protein must leave the nucleus after binding an export receptor. Which signal would most directly support this transport?

Protein import and export through Nuclear pore complex Medium
A. Actin-binding domain
B. Nuclear localization signal
C. Nuclear export signal
D. Microtubule plus-end cap

39 A transcription factor is retained in the cytoplasm when a signaling pathway keeps it bound to an inhibitory protein. How does this regulation work?

Regulation of Nuclear protein import and export Medium
A. The inhibitor depolymerizes all nuclear lamins
B. The inhibitor changes importin into a microtubule motor
C. The inhibitor converts the nuclear pore into a lipid channel
D. The inhibitor masks the transcription factor's nuclear localization signal

40 Why is the Ran-GTP/Ran-GDP gradient important for directional nuclear transport?

Regulation of Nuclear protein import and export Medium
A. It provides spatial information that controls receptor-cargo binding
B. It polymerizes the nuclear lamina during interphase
C. It supplies ATP directly to nuclear pore complexes
D. It creates actin filaments inside the nuclear envelope

41 A cell expresses a tubulin mutant that retains GTP binding but cannot hydrolyze tubulin-bound GTP after polymerization. Which phenotype is most likely?

Structure and functions of Microtubules Hard
A. Microtubules assemble only from intermediate filaments
B. Microtubules lose polarity but retain normal length
C. Microtubules become shorter and more dynamic
D. Microtubules become unusually stable and resist catastrophe

42 A drug selectively prevents microtubule minus ends from being anchored at centrosomes but does not affect tubulin polymerization. Which consequence is most likely in a migrating animal cell?

Structure and functions of Microtubules Hard
A. Permanent activation of myosin contraction
B. Loss of all actin-based protrusions
C. Conversion of microtubules into intermediate filaments
D. Randomization of microtubule array orientation

43 A vesicle normally transported toward the cell center continues moving after dynein inhibition but accumulates near the cell cortex. Which interpretation best explains the result?

Structure and functions of Microtubules Hard
A. Dynein drives transport toward microtubule plus ends
B. Kinesin drives transport toward microtubule plus ends
C. Actin treadmilling reverses microtubule polarity
D. Myosin drives transport along microtubule plus ends

44 A mitotic cell is treated with a compound that suppresses microtubule catastrophe but leaves kinetochore attachment intact. Which defect is most likely?

Structure and functions of Microtubules Hard
A. Failure to assemble intermediate filament dimers
B. Failure to form nuclear pores
C. Failure to correct improper kinetochore attachments
D. Failure to synthesize actin monomers

45 A keratin mutation prevents formation of stable lateral interactions between keratin tetramers but does not affect keratin expression. Which cellular property is most directly compromised?

Intermediate filaments and Actin Filaments Hard
A. Chromosome attachment to kinetochores
B. Resistance to tensile stress
C. GTP-dependent microtubule growth
D. ATP-dependent vesicle transport

46 A nonhydrolyzable ATP-actin analog is incorporated into a growing filament. Compared with normal actin, what is the most likely effect?

Intermediate filaments and Actin Filaments Hard
A. Altered treadmilling dynamics
B. Reduced filament polarity
C. Conversion of actin into a microtubule
D. Loss of all actin-myosin binding

47 A cell has normal actin polymerization but lacks functional profilin. Which process is most likely impaired under conditions requiring rapid filament growth?

Intermediate filaments and Actin Filaments Hard
A. Keratin filament cross-linking
B. Dynein movement toward microtubule minus ends
C. Nuclear lamina disassembly
D. Delivery of ATP-actin to growing barbed ends

48 A migrating cell expresses a constitutively active cofilin phosphatase. Which outcome is most likely if cofilin remains persistently active?

Intermediate filaments and Actin Filaments Hard
A. Enhanced actin turnover and network remodeling
B. Reduced actin filament severing
C. Selective depolymerization of microtubules
D. Permanent stabilization of stress fibers

49 A mutation removes the cytoplasmic filaments of the nuclear pore complex but leaves the central channel intact. Which defect is most likely?

Nuclear Envelope- structure of nuclear pore complex Hard
A. Impaired initial capture of import cargo
B. Complete loss of Ran-GTP production
C. Failure of inner nuclear membrane lipid synthesis
D. Loss of nuclear-envelope membrane continuity

50 A nuclear pore complex retains its scaffold but has altered phenylalanine-glycine-rich nucleoporins that no longer form a selective permeability barrier. Which result is expected?

Nuclear Envelope- structure of nuclear pore complex Hard
A. Small molecules become unable to diffuse
B. Macromolecular selectivity is reduced
C. Ribosomes become permanently attached to lamins
D. The nuclear envelope becomes a single membrane

51 A cell contains normal nuclear pores but develops a mutation that prevents fusion of the inner and outer nuclear membranes at pore sites. What is the direct consequence?

Nuclear Envelope- structure of nuclear pore complex Hard
A. Actin filaments cannot nucleate
B. Chromatin cannot bind histones
C. Lamins cannot undergo phosphorylation
D. Pores cannot create continuous transport channels

52 A lamin mutant cannot be phosphorylated during mitosis but retains normal polymerization in interphase. Which phenotype is most likely?

Nuclear lamina Hard
A. Inability of ribosomes to enter the cytoplasm
B. Persistent nuclear-lamina association during mitosis
C. Loss of all nuclear pore complexes during interphase
D. Failure of actin polymerization at the cortex

53 A mutation weakens lamin attachment to chromatin without changing lamin abundance. Which nuclear defect is most plausible?

Nuclear lamina Hard
A. Failure of mitochondrial protein import
B. Increased microtubule catastrophe at centrosomes
C. Loss of actin polarity at the leading edge
D. Altered peripheral heterochromatin organization

54 A nucleus has a mechanically defective lamina but normal nuclear pores and normal chromatin composition. Which cellular response is most likely after repeated mechanical stress?

Nuclear lamina Hard
A. Conversion of lamins into actin filaments
B. Permanent activation of kinesin motors
C. Complete inhibition of cytoplasmic translation
D. Increased nuclear deformation and envelope rupture

55 A nuclear protein contains a functional nuclear localization signal, but its import receptor cannot bind Ran-GTP. Which outcome is most likely?

Protein import and export through Nuclear pore complex Hard
A. Cargo is exported efficiently through CRM1
B. Cargo crosses the lipid bilayer without a pore
C. Import becomes independent of the Ran gradient
D. Import can occur, but receptor recycling and cargo release are disrupted

56 A protein lacking a classical nuclear localization signal is nevertheless imported efficiently when bound to a partner containing such a signal. What mechanism explains this result?

Protein import and export through Nuclear pore complex Hard
A. Direct transport by cytoplasmic dynein
B. Piggyback import through an import-competent complex
C. Passive diffusion through the lipid bilayer
D. Export followed by spontaneous nuclear assembly

57 A nuclear export cargo binds its export receptor only in the presence of Ran-GTP. If Ran-GTP is experimentally depleted from the nucleus, what happens first?

Protein import and export through Nuclear pore complex Hard
A. The nuclear envelope immediately dissolves
B. FG-repeat nucleoporins become membrane proteins
C. Nuclear import becomes receptor-independent
D. Export complex formation decreases

58 A transcription factor is phosphorylated near its nuclear localization signal, reducing importin binding. What regulatory outcome is most likely?

Regulation of Nuclear protein import and export Hard
A. Uncoupling of Ran from GTP hydrolysis
B. Constitutive nuclear accumulation
C. Irreversible degradation of all importins
D. Cytoplasmic retention of the transcription factor

59 A signaling pathway inhibits the cytoplasmic Ran-GAP while leaving nuclear Ran-GEF active. Which change is expected in the Ran system?

Regulation of Nuclear protein import and export Hard
A. An increased Ran-GTP gradient across the envelope
B. Ran becomes an integral membrane protein
C. A reduced Ran-GTP gradient across the envelope
D. Complete loss of nuclear Ran-GTP

60 A nuclear export signal is exposed only after ligand binding causes a conformational change in a regulatory protein. Which prediction is most appropriate?

Regulation of Nuclear protein import and export Hard
A. Ligand binding must block all passage through nuclear pores
B. Ligand binding can switch the protein from nuclear retention to export
C. The export receptor will hydrolyze ATP to open the pore
D. The protein will enter the nucleus only by passive diffusion