Chapter 18 Questions MCB Exam 4

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Consider an animal cell that has eight chromosomes (four pairs of homologous chromosomes) in G1 phase. How many of each of the following structures will the cell have at mitotic prophase? A. Centromeres

16

Consider an animal cell that has eight chromosomes (four pairs of homologous chromosomes) in G1 phase. How many of each of the following structures will the cell have at mitotic prophase? A. Kinetochores

16

Consider an animal cell that has eight chromosomes (four pairs of homologous chromosomes) in G1 phase. How many of each of the following structures will the cell have at mitotic prophase? A. sister chromatids

16

A friend declares that chromosomes are held at the metaphase plate by microtubules that push on each chromosome from opposite sides. Which of the following observations does not support your belief that the microtubules are pulling on the chromosomes? (a) the jiggling movement of chromosomes at the metaphase plate (b) the way in which chromosomes behave when the attachment between sister chromatids is severed (c) the way in which chromosomes behave when the attachment to one kinetochore is severed (d) the shape of chromosomes as they move toward the spindle poles at anaphase

A

Cells in the G0 state ________________. (a) do not divide. (b) cannot re-enter the cell cycle. (c) have entered this arrest state from either G1 or G2. (d) have duplicated their DNA.

A

Cytokinesis in animal cells ________________. (a) requires ATP. (b) leaves a small circular "scar" of actin filaments on the inner surface of the plasma membrane. (c) is often followed by phosphorylation of integrins in the plasma membrane. (d) is assisted by motor proteins that pull on microtubules attached to the cell cortex.

A

Mitogens are _____. (a) extracellular signals that stimulate cell division. (b) transcription factors important for cyclin production. (c) kinases that cause cells to grow in size. (d) produced by mitotic cells to keep nearby neighboring cells from dividing.

A

Programmed cell death occurs ________________. (a) by means of an intracellular suicide program. (b) rarely and selectively only during animal development. (c) only in unhealthy or abnormal cells. (d) only during embryonic development.

A

Which of the following does not occur during M phase in animal cells? (a) growth of the cell (b) condensation of chromosomes (c) breakdown of nuclear envelope (d) attachment of chromosomes to microtubules

A

Which of the following precede the re-formation of the nuclear envelope during M phase in animal cells? (a) assembly of the contractile ring (b) decondensation of chromosomes (c) reassembly of the nuclear lamina (d) transcription of nuclear genes

A

Which of the following statements about kinetochores is true? (a) Kinetochores assemble onto chromosomes during late prophase. (b) Kinetochores contain DNA-binding proteins that recognize sequences at the telomere of the chromosome. (c) Kinetochore proteins bind to the tubulin molecules at the minus end of microtubules. (d) Kinetochores assemble on chromosomes that lack centromeres.

A

Which of the following statements about the cell cycle is false? (a) Once a cell decides to enter the cell cycle, the time from start to finish is the same in all eukaryotic cells. (b) An unfavorable environment can cause cells to arrest in G1. (c) A cell has more DNA during G2 than it did in G1. (d) The cleavage divisions that occur in an early embryo have short G1 and G2 phases.

A

A cell with nuclear lamins that cannot be phosphorylated in M phase will be unable to ________________. (a) reassemble its nuclear envelope at telophase. (b) disassemble its nuclear lamina at prometaphase. (c) begin to assemble a mitotic spindle. (d) condense its chromosomes at prophase.

B

Progression through the cell cycle requires a cyclin to bind to a Cdk because _________. (a) the cyclins are the molecules with the enzymatic activity in the complex. (b) the binding of a cyclin to Cdk is required for Cdk enzymatic activity. (c) cyclin binding inhibits Cdk activity until the appropriate time in the cell cycle. (d) without cyclin binding, a cell-cycle checkpoint will be activated.

B

Which of the following events does not usually occur during interphase? (a) Cells grow in size. (b) The nuclear envelope breaks down. (c) DNA is replicated. (d) The centrosomes are duplicated.

B

Which of the following statements is false? (a) DNA synthesis begins at origins of replication. (b) The loading of the origin recognition complexes (ORCs) is triggered by S-Cdk. (c) The phosphorylation and degradation of Cdc6 help to ensure that DNA is replicated only once in each cell cycle. (d) DNA synthesis can only begin after prereplicative complexes assemble on the ORCs.

B

Which organelle fragments during mitosis? (a) endoplasmic reticulum (b) Golgi apparatus (c) mitochondrion (d) chloroplast

B

You create cells with a version of Cdc6 that cannot be phosphorylated and thus cannot be degraded. Which of the following statements describes the likely consequence of this change in Cdc6? (a) Cells will enter S phase prematurely. (b) Cells will be unable to complete DNA synthesis. (c) The origin recognition complex (ORC) will be unable to bind to DNA. (d) Cdc6 will be produced inappropriately during M phase.

B

You have isolated a strain of mutant yeast cells that divides normally at 30°C but cannot enter M phase at 37°C. You have isolated its mitotic cyclin and mitotic Cdk and find that both proteins are produced and can form a normal M-Cdk complex at both temperatures. Which of the following temperature-sensitive mutations could not be responsible for the behavior of this strain of yeast? (a) inactivation of a protein kinase that acts on the mitotic Cdk kinase (b) inactivation of an enzyme that ubiquitylates M cyclin (c) inactivation of a phosphatase that acts on the mitotic Cdk kinase (d) a decrease in the levels of a transcriptional regulator required for producing sufficient amounts of M cyclin

B

Disassembly of the nuclear envelope ________________. (a) causes the inner nuclear membrane to separate from the outer nuclear membrane. (b) results in the conversion of the nuclear envelope into protein-free membrane vesicles. (c) is triggered by the phosphorylation of integrins. (d) must occur for kinetochore microtubules to form in animal cells.

D

In which phase of the cell cycle do cells check to determine whether the DNA is fully and correctly replicated? (a) at the transition between G1 and S (b) when cells enter G0 (c) during M (d) at the end of G2

D

Levels of Cdk activity change during the cell cycle, in part because ________________. (a) the Cdks phosphorylate each other. (b) the Cdks activate the cyclins. (c) Cdk degradation precedes entry into the next phase of the cell cycle. (d) cyclin levels change during the cycle.

D

MPF activity was discovered when cytoplasm from a Xenopus M-phase cell was injected into Xenopus oocytes, inducing the oocytes to form a mitotic spindle. In a control experiment, Xenopus interphase cytoplasm was injected into oocytes and shown not to induce the formation of a mitotic spindle. Which of the following statements is not a legitimate conclusion from the control experiment? (a) The piercing of the oocyte membrane by a needle is insufficient to cause mitotic spindle formation. (b) An increased volume of cytoplasm is insufficient to cause mitotic spindle formation. (c) Injection of extra RNA molecules is insufficient to cause mitotic spindle formation. (d) Components of an interphase nucleus are insufficient to cause mitotic spindle formation.

D

The G1 DNA damage checkpoint ________________. (a) causes cells to proceed through S phase more quickly. (b) involves the degradation of p53. (c) is activated by errors caused during DNA replication. (d) involves the inhibition of cyclin-Cdk complexes by p21.

D

What would be the most obvious outcome of repeated cell cycles consisting of S phase and M phase only? (a) Cells would not be able to replicate their DNA. (b) The mitotic spindle could not assemble. (c) Cells would get larger and larger. (d) The cells produced would get smaller and smaller.

D

When introduced into mitotic cells, which of the following is expected to impair anaphase B but not anaphase A? (a) an antibody against myosin (b) ATPγS, a nonhydrolyzable ATP analog that binds to and inhibits ATPases (c) an antibody against the motor proteins that move from the plus end of microtubules to the minus end (d) an antibody against the motor proteins that move from the minus end of microtubules toward the plus end

D

Which of the following is not good direct evidence that the cell-cycle control system is conserved through billions of years of divergent evolution? (a) A yeast cell lacking a Cdk function can use the human Cdk to substitute for its missing Cdk during the cell cycle. (b) The amino acid sequences of cyclins in plants are similar to the amino acid sequences of cyclins in humans. (c) The Cdk proteins in humans share conserved phosphorylation sites with the Cdk proteins in yeast. (d) Yeast cells have only one Cdk, whereas humans have many Cdks.

D

Which of the following statements about apoptosis is true? (a) Cells that constitutively express Bcl2 will be more prone to undergo apoptosis. (b) The prodomain of procaspases contains the catalytic activity necessary for procaspase activation. (c) Bax and Bak promote apoptosis by binding to procaspases in the apoptosome. (d) Apoptosis is promoted by the release of cytochrome c into the cytosol from mitochondria.

D

Which of the following statements is false? (a) Cytokinesis in plant cells is mediated by the microtubule cytoskeleton. (b) Small membrane vesicles derived from the Golgi apparatus deliver new cell-wall material for the new wall of the dividing cell. (c) The phragmoplast forms from the remains of interpolar microtubules of the mitotic spindle. (d) Motor proteins walking along the cytoskeleton are important for the contractile ring that guides formation of the new cell wall.

D

Which of the following statements is false? (a) Mitotic Cdk must be phosphorylated by an activating kinase (Cak) before it is active. (b) Phosphorylation of mitotic Cdk by the inhibitory kinase (Wee1) makes the Cdk inactive, even if it is phosphorylated by the activating kinase. (c) Active M-Cdk phosphorylates the activating phosphatase (Cdc25) in a positive feedback loop. (d) The activating phosphatase (Cdc25) removes all phosphates from mitotic Cdk so that M-Cdk will be active.

D

Which of the following statements is false? (a) The cleavage furrow is a puckering of the plasma membrane caused by the constriction of a ring of filaments attached to the plasma membrane. (b) The cleavage furrow will not begin to form in the absence of a mitotic spindle. (c) The cleavage furrow always forms perpendicular to the interpolar microtubules. (d) The cleavage furrow always forms in the middle of the cell.

D

Which of the following statements is true? (a) Anaphase A must be completed before anaphase B can take place. (b) In cells in which anaphase B predominates, the spindle will elongate much less than in cells in which anaphase A dominates. (c) In anaphase A, both kinetochore and interpolar microtubules shorten. (d) In anaphase B, microtubules associated with the cell cortex shorten.

D

The number of cells in an adult tissue or animal depends on cell proliferation. What else does it depend on?

Programmed cell death also influences cell numbers. Most animal cells require survival signals from other cells to avoid programmed cell death, so that the levels of such signals can help determine how many cells live and how many die.

Condensins ________________. (a) are degraded when cells enter M phase. (b) assemble into complexes on the DNA when phosphorylated by M-Cdk. (c) are involved in holding sister chromatids together. (d) bind to DNA before DNA replication begins.

b

At the end of DNA replication, the sister chromatids are held together by the ___________. (a) kinetochores. (b) securins. (c) cohesins. (d) histones.

c

Which of the following statements is true? (a) The mitotic spindle is largely made of intermediate filaments. (b) The contractile ring is made largely of microtubules and actin filaments. (c) The contractile ring divides the nucleus in two. (d) The mitotic spindle helps segregate the chromosomes to the two daughter cells.

d

Which of the following descriptions is consistent with the behavior of a cell that lacks a protein required for a checkpoint mechanism that operates in G2? (a) The cell would be unable to enter M phase. (b) The cell would be unable to enter G2. (c) The cell would enter M phase under conditions when normal cells would not. (d) The cell would pass through M phase more slowly than normal cells

C

Consider an animal cell that has eight chromosomes (four pairs of homologous chromosomes) in G1 phase. How many of each of the following structures will the cell have at mitotic prophase? A. Centrosomes

2

Consider an animal cell that has eight chromosomes (four pairs of homologous chromosomes) in G1 phase. How many of each of the following structures will the cell have at mitotic prophase? A. Centrioles

4

Of the following mutations, which are likely to cause cell-cycle arrest? A. a mutation in a gene encoding a cell-surface mitogen receptor that makes the receptor active even in the absence of the mitogen B. a mutation that destroyed the kinase activity of S-Cdk C. a mutation that allowed G1-Cdk to be active independently of its phosphorylation status D. a mutation that removed the phosphorylation sites on the Rb protein E. a mutation that inhibited the activity of Rb

B, D

Irradiated mammalian cells usually stop dividing and arrest at a G1 checkpoint. Place the following events in the order in which they occur. A. production of p21 B. DNA damage C. inhibition of cyclin-Cdk complexes D. accumulation and activation of p53

B, D, A, C

Which of the following statements about the anaphase-promoting complex (APC) is false? (a) It promotes the degradation of proteins that regulate M phase. (b) It inhibits M-Cdk activity. (c) It is continuously active throughout the cell cycle. (d) M-Cdk stimulates its activity.

C

You engineer yeast cells that express the M cyclin during S phase by replacing the promoter sequence of the M cyclin gene with that of S cyclin. Keeping in mind that yeast cells have one common Cdk that binds to all cyclins, which of the following outcomes is least likely during this experiment? (a) There will be both M cyclin-Cdk and S cyclin-Cdk complexes in the cell during S phase. (b) Some substrates that are normally phosphorylated in M phase will now be phosphorylated in S phase. (c) G1 cyclins will be expressed during S phase. (d) S-Cdk targets will be phosphorylated during S phase.

C

Apoptosis differs from necrosis in that necrosis ________________. (a) requires the reception of an extracellular signal. (b) causes DNA to fragment. (c) causes cells to swell and burst, whereas apoptotic cells shrink and condense. (d) involves a caspase cascade.

C

How does S-Cdk help guarantee that replication occurs only once during each cell cycle? (a) It blocks the rise of Cdc6 concentrations early in G1. (b) It phosphorylates and inactivates DNA helicase. (c) It phosphorylates the Cdc6 protein, marking it for destruction. (d) It promotes the assembly of a prereplicative complex.

C

The Retinoblastoma (Rb) protein blocks cells from entering the cell cycle by ______. (a) phosphorylating Cdk. (b) marking cyclins for destruction by proteolysis. (c) inhibiting cyclin transcription. (d) activating apoptosis.

C

The concentration of mitotic cyclin (M cyclin) ________________. (a) rises markedly during M phase. (b) is activated by phosphorylation. (c) falls toward the end of M phase as a result of ubiquitylation and degradation. (d) is highest in G1 phase.

C

Before chromosomes segregate in M phase, they and the segregation machinery must be appropriately prepared. Indicate whether the following statements are true or false Cohesins are required to make the chromosomes more compact and thus to prevent tangling between different chromosomes.

False. Condensins are required to make the chromosomes more compact and thus to prevent tangling between different chromosomes.

Before chromosomes segregate in M phase, they and the segregation machinery must be appropriately prepared. Indicate whether the following statements are true or false Sister chromatids are held together by condensins from the time they arise by DNA replication until the time they separate at anaphase.

False. Sister chromatids are held together by cohesins from the time they arise by DNA replication until the time they separate at anaphase.

Are the statements below true or false? Explain your answer. Statement 2: Therefore, the cell-cycle control system operates primarily by a timing mechanism, in which the entry into one phase starts a timer set for sufficient time to complete the required tasks. After a given amount of time has elapsed, a molecular "alarm" triggers movement to the next phase.

False. The cell-cycle control system does use a timing mechanism of sorts, but it also employs various surveillance and feedback mechanisms (checkpoints). Cells will not embark on later events or phases until the earlier events or phases have been completed successfully. In response to a defect or a delay in a cell-cycle event, cells engage molecular brakes to arrest the progression of the cell cycle at various checkpoints, to allow time for completion or repair.

Before chromosomes segregate in M phase, they and the segregation machinery must be appropriately prepared. Indicate whether the following statements are true or false The centromere nucleates a radial array of microtubules called an aster, and its duplication is triggered by S-Cdk.

False. The centrosome nucleates a radial array of microtubules called an aster, and its duplication is triggered by S-Cdk.

Before chromosomes segregate in M phase, they and the segregation machinery must be appropriately prepared. Indicate whether the following statements are true or false. The mitotic spindle is composed of actin filaments and myosin filaments

False. The contractile ring is composed of actin filaments and myosin filaments.

What is the cause of the massive amount of programmed cell death of nerve cells (neurons) that occurs in the developing vertebrate nervous system, and what purpose does it serve?

Immature neurons are produced in excess of the number that will eventually be required. They compete for the limited amount of survival factors secreted by the target cells they contact. Those cells that fail to get enough survival factor undergo programmed cell death. Up to half or more of the original nerve cells die in this way. This competitive mechanism helps match the number of developing nerve cells to the number of target cells they contact.

What is the main molecular difference between cells in a G0 state and cells that have simply paused in G1?

In G0, the cell-cycle control system is partly dismantled, so that some of the Cdks and cyclins are not present. Cells paused in G1, by contrast, still contain all the components of the cell-cycle control system. Whereas the latter cells can rapidly progress through the cycle when conditions are right, G0 cells need to synthesize the missing cell-cycle control proteins so as to re-enter the cycle, which usually takes 8 hours or more.

Why should it be that drugs such as colchicine, which inhibit microtubule polymerization, and drugs such as Taxol®, which stabilize microtubules, both inhibit mitosis?

Mitosis requires that the spindle microtubules behave dynamically—continuously polymerizing and depolymerizing—to probe the cell cortex, to seek attachments to kinetochores, and to segregate the chromosomes. Static microtubules are unable to do any of these things.

What would happen to the progeny of a cell that proceeded to mitosis and cell division after entering S phase but had not completed S phase? Keep in mind that highly condensed chromatin, including the centromere region, is replicated late in S phase. Explain your answer.

The daughter cells would probably die. Those chromosomes that had not completed replication in S phase would have only one centromere, because the centromere is the last part of the chromosome to be replicated; the chromosome would therefore be segregated to only one of the two daughter cells at random. At least one, and probably both, of the daughter cells would thus receive an incomplete set of chromosomes and would be unlikely to be viable. Even if one daughter cell, by chance, received a full set of chromosomes, some of these chromosomes would be incompletely replicated and the cell would probably still not be viable.

For each of the following sentences, fill in the blanks with the best word or phrase

The four phases of the cell cycle, in order, are G1, S, M, and G2. A cell contains the most DNA after S phase of the cell cycle. A cell is smallest in size after M phase of the cell cycle. Growth occurs in G1, S, and G2 phases of the cell cycle. A cell does not enter mitosis until it has completed DNA synthesis.

You have isolated a mutant in which a fraction of the new cells die soon after cell division and a fraction of the living cells have an extra copy of one or more chromosomes. When you grow the cells under conditions in which they transit the cell cycle more slowly, the defect disappears, suggesting that the mitotic spindle and segregation machinery are normal. Propose a basis for the defect.

This mutant may be lacking the checkpoint mechanism that delays the onset of anaphase and chromosome segregation until all chromosomes have attached properly to the mitotic spindle. If cells attempt chromosome segregation before all chromosomes have attached properly, some of the daughter cells will receive too few chromosomes (and thus will probably die) and other cells will receive additional chromosomes. Normally, cells use such a surveillance system to monitor the spindle attachment of each chromosome and engage molecular brakes until all chromosomes have attached properly. The molecular brakes will be dispensable in some dividing cells if all of the chromosomes rapidly become properly attached to the spindle. In other dividing cells, it will take longer for some of the chromosomes to find their appropriate attachments, and thus the molecular brakes will be essential to ensure faithful segregation of the duplicated copies of each chromosome to the two daughter cells. Slowing the cycle will allow more cells to segregate their chromosomes properly even in the absence of this "spindle attachment" checkpoint.

Before chromosomes segregate in M phase, they and the segregation machinery must be appropriately prepared. Indicate whether the following statements are true or false Each centrosome contains a pair of centrioles and hundreds of γ-tubulin rings that nucleate the growth of microtubules.

True

Before chromosomes segregate in M phase, they and the segregation machinery must be appropriately prepared. Indicate whether the following statements are true or false Microtubule-dependent motor proteins and microtubule polymerization and depolymerization are mainly responsible for the organized movements of chromosomes during mitosis.

True

Is the following statement true or false? After the nuclear envelope breaks down, microtubules gain access to the chromosomes and, every so often, a randomly probing microtubule captures a chromosome and ultimately connects to the kinetochore to become a kinetochore microtubule of the spindle.

True

Are the statements below true or false? Explain your answer. Statement 1: Generally, in a given organism, the S, G2, and M phases of the cell cycle take a defined and stereotyped amount of time in most cells.

True. In nearly all cells in an organism, the S, G2, and M phases of the cell cycle take the same amount of time. The different timing of cell division in different cell types is due to variable lengths of the G1 phase or to withdrawal into the G0 state.

The principal microtubule-organizing center in animal cells is the ____________. (a) centrosome. (b) centromere. (c) kinetochore. (d) cell cortex.

a


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