Unit 2: Cellular Transport and Trafficking; Cell Cycle and its Regulation - Practice Quiz

BTY426 — Cell And Molecular Biology 60 Questions
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1 Which type of transport moves molecules across a membrane against their concentration gradient and requires energy?

Molecular mechanisms of membrane transport Easy
A. Facilitated diffusion
B. Simple diffusion
C. Active transport
D. Osmosis

2 The pump transports which ions in each cycle?

Molecular mechanisms of membrane transport Easy
A. 3 out and 2 in
B. 2 out and 3 in
C. 2 out and 2 in
D. 3 out and 2 in

3 Which molecule can most easily cross a lipid bilayer by simple diffusion?

Molecular mechanisms of membrane transport Easy
A. Glucose
B.
C.
D.

4 A channel protein that allows only water molecules to pass across the membrane is called a(n):

Molecular mechanisms of membrane transport Easy
A. Antiporter
B. Aquaporin
C. ATPase
D. Symporter

5 A transporter that moves two different molecules in opposite directions across a membrane is called a(n):

Molecular mechanisms of membrane transport Easy
A. Ionophore
B. Symporter
C. Antiporter
D. Uniporter

6 Molecules move between the nucleus and cytoplasm through which structure?

Nuclear transport Easy
A. Centriole
B. Nuclear pore complex
C. Ribosome
D. Nucleolus

7 A short amino acid sequence that directs a protein into the nucleus is called a:

Nuclear transport Easy
A. Poly-A tail
B. TATA box
C. Nuclear localization signal (NLS)
D. Signal peptide

8 Which small GTPase provides directionality to nuclear transport?

Nuclear transport Easy
A. Rho
B. Ran
C. Ras
D. Rab

9 The receptor proteins that carry cargo through nuclear pores are collectively called:

Nuclear transport Easy
A. Dyneins
B. Karyopherins
C. Clathrins
D. Kinesins

10 Most proteins imported into mitochondria are synthesized:

Transport across mitochondria and chloroplasts Easy
A. Inside the mitochondrial matrix
B. On free cytosolic ribosomes
C. In the Golgi apparatus
D. Within the nucleus

11 The protein complex in the mitochondrial outer membrane that imports proteins is the:

Transport across mitochondria and chloroplasts Easy
A. TOM complex
B. TIM complex
C. TOC complex
D. SEC complex

12 Protein import into chloroplasts occurs through the TOC and TIC complexes located in the:

Transport across mitochondria and chloroplasts Easy
A. Stroma
B. Cytosol
C. Thylakoid membrane
D. Outer and inner envelope membranes

13 Proteins destined for mitochondria typically carry a targeting sequence at their:

Transport across mitochondria and chloroplasts Easy
A. C-terminus
B. Both ends
C. N-terminus
D. Middle

14 In the secretory pathway, proteins follow which correct order of movement?

Intracellular vesicular trafficking from endoplasmic reticulum through Golgi apparatus to lysosomes/cell exterior Easy
A. Plasma membrane → Golgi → ER
B. ER → Golgi → plasma membrane
C. ER → lysosome → Golgi
D. Golgi → ER → plasma membrane

15 Which coat protein forms vesicles that transport cargo from the ER to the Golgi?

Intracellular vesicular trafficking from endoplasmic reticulum through Golgi apparatus to lysosomes/cell exterior Easy
A. Clathrin
B. Caveolin
C. COPI
D. COPII

16 Which coat protein is mainly involved in vesicle formation during receptor-mediated endocytosis?

Intracellular vesicular trafficking from endoplasmic reticulum through Golgi apparatus to lysosomes/cell exterior Easy
A. COPI
B. COPII
C. Clathrin
D. Dynamin

17 Proteins that mediate the fusion of transport vesicles with their target membranes are called:

Intracellular vesicular trafficking from endoplasmic reticulum through Golgi apparatus to lysosomes/cell exterior Easy
A. Kinesins
B. SNAREs
C. Cadherins
D. Integrins

18 Which organelle contains hydrolytic enzymes for the breakdown of macromolecules?

Intracellular vesicular trafficking from endoplasmic reticulum through Golgi apparatus to lysosomes/cell exterior Easy
A. Peroxisome
B. Ribosome
C. Lysosome
D. Centrosome

19 During which phase of the cell cycle does DNA replication occur?

Cell cycle and its regulation: mitosis, meiosis and cytokinesis Easy
A. M phase
B. S phase
C. phase
D. phase

20 Which enzymes drive progression through the cell cycle by binding to cyclins?

Cell cycle and its regulation: mitosis, meiosis and cytokinesis Easy
A. Cyclin-dependent kinases (CDKs)
B. Phosphatases
C. DNA polymerases
D. Helicases

21 A cell maintains a high internal concentration and low internal concentration using the -ATPase. If a drug blocks ATP hydrolysis by this pump, which secondary effect is most likely to occur first?

Molecular mechanisms of membrane transport Medium
A. Direct inhibition of facilitated diffusion of glucose
B. Immediate lysis of the cell due to osmotic influx of water
C. Collapse of the electrochemical gradient driving -coupled glucose uptake
D. Increased activity of voltage-gated channels

22 A researcher observes that a solute crosses a membrane down its concentration gradient, shows saturation kinetics at high solute concentration, and requires no ATP. Which transport mechanism best explains these observations?

Molecular mechanisms of membrane transport Medium
A. Facilitated diffusion through a carrier protein
B. Secondary active transport (antiport)
C. Simple diffusion through the lipid bilayer
D. Primary active transport

23 The exchanger in cardiac cells extrudes one ion while importing three ions. This is best classified as:

Molecular mechanisms of membrane transport Medium
A. Secondary active transport (symport)
B. Primary active transport
C. Secondary active transport (antiport)
D. Facilitated diffusion

24 In red blood cells, the band 3 protein exchanges for across the membrane without energy input, and net movement can go either direction depending on gradients. This process is:

Molecular mechanisms of membrane transport Medium
A. Simple diffusion of ions
B. Facilitated diffusion via an anion exchanger
C. Endocytosis of bicarbonate
D. Primary active transport

25 A protein of kDa lacks a nuclear localization signal (NLS). What is the most likely outcome regarding its distribution?

nuclear transport Medium
A. It accumulates in the nucleolus via ribosomal targeting
B. It remains in the cytoplasm because it is too large to passively diffuse through the nuclear pore
C. It freely diffuses into the nucleus through the nuclear pore complex
D. It is actively exported to the nucleus by importins

26 The directionality of nuclear import is maintained by the Ran GTPase system. Which condition holds in the nucleus to promote cargo release from importin?

nuclear transport Medium
A. Ran-GTP is hydrolyzed to trap cargo in the cytoplasm
B. Absence of Ran promotes cargo binding to importin
C. High Ran-GDP concentration stabilizes the importin-cargo complex
D. High Ran-GTP concentration binds importin and releases the cargo

27 Exportins recognize cargo bearing a nuclear export signal (NES) only when bound to Ran-GTP. Once the complex reaches the cytoplasm, what triggers cargo release?

nuclear transport Medium
A. Increased cytoplasmic Ran-GTP concentration
B. Phosphorylation of the NES by cytoplasmic kinases
C. Binding of additional importin molecules in the cytoplasm
D. Hydrolysis of Ran-GTP to Ran-GDP stimulated by cytoplasmic RanGAP

28 A mitochondrial matrix protein is synthesized in the cytosol with an N-terminal presequence. Which feature of this presequence is essential for its import through the TOM and TIM23 complexes?

transport across mitochondria and chloroplasts Medium
A. A hydrophobic stretch that anchors it in the outer membrane
B. A C-terminal KDEL retention motif
C. A mannose-6-phosphate tag added in the cytosol
D. An amphipathic -helix with positively charged residues

29 The import of nuclear-encoded proteins into the mitochondrial matrix requires energy from two sources. These are:

transport across mitochondria and chloroplasts Medium
A. ATP hydrolysis by the ATP synthase alone
B. GTP hydrolysis by Ran and the proton gradient
C. The outer membrane potential and cytosolic Hsp90
D. The inner membrane potential () and ATP hydrolysis by mtHsp70

30 Unlike mitochondrial matrix import, protein import into the chloroplast stroma via the TOC/TIC complexes relies primarily on which energy source?

transport across mitochondria and chloroplasts Medium
A. A proton-motive force generated by photosynthesis
B. ATP and GTP hydrolysis rather than a transmembrane potential
C. The inner membrane electrochemical potential like TIM23
D. The mannose-6-phosphate receptor pathway

31 Anterograde transport of newly synthesized proteins from the ER to the Golgi apparatus is mediated by which type of coated vesicle?

Intracellular vesicular trafficking from endoplasmic reticulum through Golgi apparatus to lysosomes/cell exterior Medium
A. Caveolin-coated vesicles
B. COPII-coated vesicles
C. COPI-coated vesicles
D. Clathrin-coated vesicles

32 A soluble ER-resident enzyme escapes to the Golgi. How is it retrieved back to the ER?

Intracellular vesicular trafficking from endoplasmic reticulum through Golgi apparatus to lysosomes/cell exterior Medium
A. It is retained by an NLS and imported into the nucleus
B. Its C-terminal KDEL sequence is recognized by the KDEL receptor and returned in COPI vesicles
C. Its N-terminal presequence directs it back through TOM/TIM
D. It is tagged with mannose-6-phosphate and sent to lysosomes

33 Lysosomal hydrolases are specifically targeted from the trans-Golgi network to lysosomes by which molecular tag?

Intracellular vesicular trafficking from endoplasmic reticulum through Golgi apparatus to lysosomes/cell exterior Medium
A. KDEL recognized by the KDEL receptor
B. Ubiquitin recognized by the proteasome
C. A nuclear localization signal recognized by importin
D. Mannose-6-phosphate recognized by the M6P receptor

34 The specificity of vesicle fusion with a target membrane is primarily determined by the pairing of:

Intracellular vesicular trafficking from endoplasmic reticulum through Golgi apparatus to lysosomes/cell exterior Medium
A. KDEL receptors with mannose-6-phosphate tags
B. v-SNAREs on the vesicle with cognate t-SNAREs on the target membrane
C. Rab-GDP with GDI on both membranes
D. Clathrin triskelions with adaptor proteins

35 The activity of cyclin-dependent kinases (CDKs) oscillates through the cell cycle. What primarily controls this oscillation?

Cell cycle and its regulation: mitosis, meiosis and cytokinesis Medium
A. Periodic synthesis and degradation of cyclin partners
B. Oscillation of ATP concentration in the cytosol
C. Fluctuating levels of the CDK proteins themselves
D. Changes in the number of ribosomes

36 The spindle assembly checkpoint (SAC) prevents progression from metaphase to anaphase until:

Cell cycle and its regulation: mitosis, meiosis and cytokinesis Medium
A. Cytokinesis has been initiated
B. All kinetochores are properly attached to spindle microtubules
C. All DNA has been fully replicated
D. The nuclear envelope has completely reformed

37 Separation of sister chromatids at anaphase is triggered when separase cleaves cohesin. Separase is kept inactive until this point by:

Cell cycle and its regulation: mitosis, meiosis and cytokinesis Medium
A. Sequestration inside the nucleolus
B. Phosphorylation by M-CDK
C. Binding to the inhibitory protein securin
D. Association with the KDEL receptor

38 A key difference between meiosis I and mitosis is that during meiosis I:

Cell cycle and its regulation: mitosis, meiosis and cytokinesis Medium
A. DNA replication occurs between the two divisions
B. No crossing over takes place at any stage
C. Sister chromatids separate to opposite poles
D. Homologous chromosomes separate while sister chromatids remain joined

39 In animal cell cytokinesis, the contractile ring that pinches the cell in two is composed mainly of:

Cell cycle and its regulation: mitosis, meiosis and cytokinesis Medium
A. Actin filaments and myosin II
B. Septins and clathrin
C. Intermediate filaments and keratin
D. Microtubules and dynein

40 The retinoblastoma protein (Rb) restrains the transition by binding and inhibiting E2F transcription factors. How is this restraint relieved?

Cell cycle and its regulation: mitosis, meiosis and cytokinesis Medium
A. Degradation of E2F by the APC/C
B. Binding of securin to Rb
C. Phosphorylation of Rb by /S-CDK complexes releases E2F
D. Dephosphorylation of Rb by cytoplasmic phosphatases

41 In a secondary active transport process, the symporter (SGLT1) moves 2 ions per glucose molecule. If the intracellular glucose concentration is -fold higher than extracellular, what minimum electrochemical gradient (expressed as the ratio of driving force) is theoretically required to sustain uphill glucose accumulation at , assuming membrane potential contribution is embedded in the gradient?

Molecular mechanisms of membrane transport Hard
A. The combined electrochemical energy from 2 ions must exceed
B. The combined electrochemical energy from 2 ions must exceed
C. The glucose gradient is irrelevant because symport is thermodynamically spontaneous
D. A single gradient of -fold is sufficient regardless of stoichiometry

42 The -ATPase undergoes E1/E2 conformational cycling. A mutation locks the pump preferentially in the E2-P (phosphorylated) state with high extracellular affinity but impaired dephosphorylation. What is the most direct consequence?

Molecular mechanisms of membrane transport Hard
A. The pump stalls because cannot be released into the cytoplasm
B. Continuous export accelerates due to trapped high-energy intermediate
C. ATP hydrolysis increases to compensate for the block
D. is exported instead of imported, reversing polarity

43 GLUT1 facilitates glucose uptake by alternating access. Which experimental observation would most strongly distinguish a facilitated diffusion carrier from a channel for the same solute?

Molecular mechanisms of membrane transport Hard
A. Transport requires direct ATP hydrolysis at the binding site
B. Transport shows saturation kinetics and a defined
C. Transport rate increases linearly without limit as substrate rises
D. Transport is blocked by removing the electrochemical gradient

44 Ran-GTP asymmetry drives directional nucleocytoplasmic transport. If a cell is treated to deplete RanGAP specifically at the cytoplasmic face of the NPC, what is the predicted effect on importin-mediated cargo import?

Nuclear transport Hard
A. Import halts because importin cannot recycle back to the cytoplasm to bind new cargo
B. Import reverses, exporting nuclear cargo into the cytoplasm
C. Import is impaired because cargo-importin complexes fail to dissociate efficiently in the nucleus
D. Import continues normally because RanGEF is unaffected

45 A protein of 82 kDa lacking any classical NLS is found concentrated in the nucleus at steady state. Which mechanism most plausibly explains this without invoking a canonical importin- NLS pathway?

Nuclear transport Hard
A. Active export by CRM1 concentrates it inside
B. Passive diffusion through the NPC central channel followed by nuclear retention via binding to chromatin
C. Karyopherin-independent transport is thermodynamically impossible
D. Direct passage because 82 kDa is below the NPC diffusion limit

46 The FG-repeat nucleoporins form a selective permeability barrier. According to the selective phase (hydrogel) model, how do transport receptors traverse this barrier?

Nuclear transport Hard
A. They create transient pores by displacing FG-repeats through hydrophobic interactions
B. They bind FG-repeats to locally dissolve the meshwork and diffuse through
C. They enzymatically cleave FG-repeats to open a passage
D. They are pumped through by ATP hydrolysis at the NPC scaffold

47 A mitochondrial matrix-targeted protein is engineered to fold rapidly and stably in the cytosol before reaching the TOM complex. What is the most likely outcome regarding its import?

Transport across mitochondria and chloroplasts Hard
A. Import occurs but the presequence is not cleaved
B. The protein is imported into the intermembrane space instead of the matrix
C. Import is blocked because the protein cannot be threaded through TOM/TIM23 in unfolded form
D. Import proceeds faster because the folded protein is more stable

48 TIM23-mediated import into the matrix requires two energy inputs. Which combination correctly identifies both and their roles?

Transport across mitochondria and chloroplasts Hard
A. powers the motor; GTP hydrolysis drives presequence movement
B. ATP hydrolysis at TOM drives entry; completes translocation
C. Membrane potential drives presequence translocation; matrix ATP powers the import motor (mtHsp70)
D. Only matrix ATP is required; the membrane potential is dispensable

49 Chloroplast protein import via TOC/TIC differs from mitochondrial import in its energy requirement. Which statement correctly captures a key distinction?

Transport across mitochondria and chloroplasts Hard
A. Chloroplast import requires a thylakoid membrane potential analogous to mitochondrial
B. Both organelles use identical presequence receptors and translocons
C. Chloroplast import into the stroma requires GTP at TOC and stromal ATP, without needing a membrane potential
D. Chloroplast import is entirely passive once the transit peptide binds

50 A protein carries both an N-terminal mitochondrial matrix presequence and, immediately downstream, a hydrophobic stop-transfer sequence. Where will this protein most likely localize?

Transport across mitochondria and chloroplasts Hard
A. Intermembrane space as a soluble protein after full cleavage
B. Matrix, because the presequence dominates targeting
C. Inner membrane, with the stop-transfer arresting lateral release into the lipid bilayer
D. Outer membrane, inserted by the SAM complex

51 A mutation abolishes the GTPase activity of Sar1 (locking it in the GTP-bound state) in the COPII pathway. What is the most direct consequence for ER-to-Golgi transport?

Intracellular vesicular trafficking from endoplasmic reticulum through Golgi apparatus to lysosomes/cell exterior Hard
A. Cargo is redirected to COPI-mediated retrograde transport
B. COPII vesicles never form because coat recruitment requires GTP hydrolysis
C. ER exit accelerates due to constitutive coat activity
D. COPII coats assemble but fail to disassemble, impairing vesicle uncoating and fusion

52 In I-cell disease (mucolipidosis II), lysosomal enzymes are secreted rather than delivered to lysosomes. The primary defect lies in which step?

Intracellular vesicular trafficking from endoplasmic reticulum through Golgi apparatus to lysosomes/cell exterior Hard
A. Loss of the mannose-6-phosphate receptor in the trans-Golgi
B. Defective acidification of the lysosomal lumen
C. Failure of clathrin-coated vesicle budding from the trans-Golgi
D. Deficiency of GlcNAc phosphotransferase preventing M6P tag addition

53 SNARE-mediated fusion requires specific v-SNARE/t-SNARE pairing. NSF/-SNAP function to disassemble cis-SNARE complexes. If NSF is inhibited, what accumulates and why?

Intracellular vesicular trafficking from endoplasmic reticulum through Golgi apparatus to lysosomes/cell exterior Hard
A. Uncoated vesicles accumulate because coat removal fails
B. trans-SNARE complexes accumulate because fusion cannot initiate
C. cis-SNARE complexes accumulate, depleting free SNAREs available for new rounds of fusion
D. Rab-GTP is depleted, halting tethering

54 A soluble ER-resident protein bearing a KDEL sequence is found leaking into the medium at low levels. Which mechanism best explains why most such protein is normally retained despite bulk flow toward the Golgi?

Intracellular vesicular trafficking from endoplasmic reticulum through Golgi apparatus to lysosomes/cell exterior Hard
A. KDEL proteins are covalently anchored to the ER membrane
B. KDEL prevents any exit from the ER by blocking COPII loading
C. The KDEL receptor in the cis-Golgi binds escaped proteins and returns them via COPI retrograde transport
D. The KDEL receptor exports the proteins directly out of the cell

55 The spindle assembly checkpoint (SAC) delays anaphase until all kinetochores are attached. A cell has a single unattached kinetochore. Which molecular event is directly prevented by the active SAC?

Cell cycle and its regulation: mitosis, meiosis and cytokinesis Hard
A. Cohesin loading onto sister chromatids at S phase
B. Cdk1 activation by Cdc25 phosphatase
C. Separase inhibition by securin binding
D. APC/C-Cdc20 activation, thereby blocking securin and cyclin B degradation

56 In meiosis I, sister chromatids must remain attached at the centromere while chromosome arms separate. Which mechanism protects centromeric cohesin from cleavage during meiosis I?

Cell cycle and its regulation: mitosis, meiosis and cytokinesis Hard
A. Centromeric cohesin lacks the cleavage site recognized by separase
B. Separase is completely inactivated during meiosis I
C. Condensin displaces cohesin only from the arms after cleavage
D. Shugoshin (Sgo1) recruits PP2A to dephosphorylate and protect centromeric cohesin (Rec8) from separase

57 The restriction point (R) in G1 is governed by Rb phosphorylation. A cell expresses a mutant Rb that cannot be phosphorylated by Cyclin D-Cdk4/6. What is the predicted phenotype?

Cell cycle and its regulation: mitosis, meiosis and cytokinesis Hard
A. Cells arrest in G2 due to failed E2F release
B. Cells skip G1 and enter S phase prematurely
C. Cells arrest in G1 because E2F remains sequestered and S-phase genes are not transcribed
D. Cells proliferate uncontrollably because Rb is inactive

58 Cyclin B-Cdk1 (MPF) activity rises abruptly at the G2/M transition. Which positive feedback loop explains the switch-like activation?

Cell cycle and its regulation: mitosis, meiosis and cytokinesis Hard
A. Cdk1 stabilizes its own cyclin against APC/C degradation
B. Cyclin B synthesis is triggered directly by Cdk1 autophosphorylation
C. Cdk1 activates Cdc25 (its activating phosphatase) and inhibits Wee1 (its inhibitory kinase)
D. Cdc25 inactivates Cdk1, creating a negative feedback delay

59 During cytokinesis in animal cells, positioning of the contractile ring is dictated by the mitotic spindle. Which signaling correctly describes RhoA-based furrow specification?

Cell cycle and its regulation: mitosis, meiosis and cytokinesis Hard
A. The midbody recruits dynamin to constrict the membrane independently of RhoA
B. Astral microtubules directly nucleate actin filaments at the cortex
C. The central spindle and astral microtubules position the RhoGEF Ect2, activating RhoA to assemble the actomyosin ring at the equator
D. RhoA is globally activated and locally inhibited only at the poles by Ran-GTP

60 The CFTR chloride channel is an ABC transporter family member that functions as a channel rather than a pump. Which feature explains this unusual behavior?

Molecular mechanisms of membrane transport Hard
A. It uses the gradient to conduct downhill
B. ATP binding/hydrolysis at its nucleotide-binding domains gates an open channel pore rather than driving alternating access
C. It hydrolyzes ATP to pump against its gradient like a canonical ABC pump
D. It conducts without any nucleotide involvement