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You are leading a team of researchers at a pharmaceutical company.Your goal is to design drugs that help fight cancer.Specifically,you want to focus on drugs that bind to and inactivate certain proteins,thereby halting cell cycle progression.One of your team members suggests targeting the retinoblastoma (Rb) protein and inhibiting this protein.Will this approach be successful? Why or why not?


A) This approach will not be successful.Rb is tumor-suppressor protein,and functions to inhibit the action of a number of cell cycle regulatory proteins.A drug designed to inactivate the Rb protein would essentially create the same situation as in as a cell that lacks both copies of the Rb gene.Lack of Rb activity would release the inhibition of cell cycle regulatory proteins,thereby promoting cell cycle progression,rather than halting it.
B) This approach will be successful.Rb is an oncogene,and functions to activate a number of cell cycle regulatory proteins.A drug designed to inactivate the Rb protein would halt the cell cycle in cells that contain an active Rb.As a result,cancer cells expressing a constitutively active Rb protein would be good targets for this type of therapeutic.
C) This approach will be successful.Rb is tumor-suppressor protein,and functions to inhibit the action of a number of cell cycle regulatory proteins.A drug designed to inactivate the Rb protein would activate cell cycle inhibition.Lack of Rb activity would therefore inhibit the cell cycle regulatory proteins.
D) This approach will not be successful.Rb is an oncogene,and functions to activate a number of cell cycle regulatory proteins.A drug designed to inactivate the Rb protein would actually activate cell cycle progression.As a result,this drug would likely make this situation worse for patients whose cancer cells contain mutant Rb.

E) All of the above
F) B) and D)

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The portion of the cell cycle when the cell is growing and does not contain a replicated genome is referred to as:


A) G1
B) S
C) G2
D) Mitosis
E) Cytokinesis

F) B) and D)
G) C) and D)

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In prophase,ribosomal RNA synthesis stops when the chromosomes condense,and as a result:


A) the chromosomes lengthen.
B) the nuclear envelope reforms.
C) the nucleolus disappears.
D) the chromosomes line up at the equator of the cell.

E) A) and D)
F) A) and B)

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You are conducting a genetic screen using Caenorhabditis elegans embryos to isolate mutations affecting anaphase (A) .Therefore,you need to look for embryos in which


A) the centromeres do not move toward the poles.
B) the poles do not move apart.
C) the spindle apparatus does not disassemble.
D) sister chromatids are mismatched and therefore fail to separate.

E) A) and B)
F) A) and C)

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Eukaryotic chromosomes are composed of a complex of 60% protein and 40% DNA.This complex is referred to as:


A) The histone complex
B) Chromatin
C) The kinetochore
D) Cohesin

E) A) and C)
F) None of the above

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You are studying cell cycle progression in an early frog embryo.If you were to inject a protein synthesis inhibitor into a cell during S phase,where do you predict that the cells would arrest?


A) G1
B) G2
C) Metaphase
D) Telophase

E) C) and D)
F) All of the above

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B

You are examining the effect of maturation-promoting factor (MPF) in sea urchin cells,which have a diploid number of 36.If you fuse a dividing sea urchin cell with a G1 arrested oocyte,what would be the outcome?


A) The G1 cell would enter mitosis,but would likely arrest at the spindle checkpoint because the chromosomes have not been properly replicated.
B) The G1 cell would undergo mitosis and its daughter cells would each have 36 chromosomes.
C) The G1 cell would undergo mitosis and its daughter cells would each have 18 chromosomes.
D) The G1 cell would first go through S phase and then mitosis.Its daughter cells would have 36 chromosomes.

E) All of the above
F) B) and C)

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Plant cells typically achieve cytokinesis by:


A) binary fission.
B) forming a cell plate across the middle of the cell.
C) forming a cleavage furrow that pinches the cell into two.
D) chromosome condensation.
E) chromosome elongation.

F) All of the above
G) A) and E)

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If you were to think of the cell as a car,and mitosis as a process that drives that car to go,what would be a good analogy for a cell that has a mutation in both copies of a tumor-suppressor gene?


A) The gas pedal of a car gets stuck while pushed down.
B) The gas pedal of a car does not work at all.
C) The brake pedal of a car gets stuck while pushed down.
D) The brake pedal of a car does not work at all.

E) None of the above
F) All of the above

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This stage of mitosis is characterized by the disassembly of spindle apparatus,the reestablishment of the nuclear membrane,and the decondensation of the chromosomes:


A) Prometaphase
B) Telophase
C) Anaphase
D) Metaphase

E) A) and D)
F) A) and C)

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If a cell contained a mutation in the gene that encodes FtsZ,which process would be affected?


A) Septation
B) Cytokinesis
C) Prophase
D) DNA Synthesis
E) Cohesin cleavage

F) A) and B)
G) A) and C)

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Before cell division of somatic cells,each chromosome must be replicated.After replication,the resulting two parts of each chromosome are held together by cohesin at the centromere.These two parts are referred to as:


A) Sister chromatids
B) Homologous chromosomes
C) Daughter chromosomes
D) Kinetochores
E) Genes

F) A) and C)
G) All of the above

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A

During this stage of mitosis,the nuclear envelope begins to break down and the spindle begins to form.


A) Anaphase
B) Metaphase
C) Prophase
D) Telophase
E) Prometaphase

F) C) and D)
G) All of the above

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This stage of the cell cycle is characterized by growth and it contains a checkpoint to verify that all of the DNA has been replicated prior to mitosis.


A) G1
B) S
C) G2
D) Mitosis
E) Cytokinesis

F) B) and D)
G) D) and E)

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You are assembling a model of a chromosome,but begin having some trouble when you get to the step of forming chromatin loops.If you are unable to resolve this problem,what step of chromosome structure would you be unable to achieve?


A) Histone/DNA complex
B) Nucleosome
C) Solenoid
D) Rosettes

E) All of the above
F) None of the above

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During this stage of mitosis,the chromosomes become attached to the spindle at their kinetochores.


A) Prophase
B) Prometaphase
C) Metaphase
D) Anaphase
E) Telophase

F) B) and E)
G) All of the above

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If a drug that inhibited transport from the trans face of the Golgi was applied to plant cells,which stage of the cell cycle would be directly affected?


A) G2
B) S
C) Metaphase
D) Anaphase
E) Cytokinesis

F) B) and D)
G) A) and C)

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If a cell was capable of bypassing metaphase and going directly from prometaphase to anaphase,what is the most likely consequence of this?


A) The resulting daughter cells would not have a nuclear envelope.
B) The resulting daughter cells would have significantly different quantities of cytoplasmic materials.
C) The resulting daughter cells would have different numbers of chromosomes.
D) The resulting daughter cells would be completely normal.

E) A) and D)
F) A) and C)

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A cell biologist produces a karyotype of mouse somatic cells arrested in mitosis.She sees 40 chromosomes,which is completely normal for mice.Based on this information,what is the haploid number of chromosomes for mice?


A) 10
B) 20
C) 40
D) 80
E) It cannot be determined from the information provided.

F) A) and D)
G) A) and C)

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B

Why is it so important that all of the chromosomes align on the metaphase plate during metaphase?


A) This is the only place in the cell where the cyclins and Cdks are located.
B) If they cannot,it suggests that they aren't properly attached to the spindle microtubules,and thus won't separate properly during anaphase.
C) This is the location where the chromosomes can become attached to the spindle microtubules.
D) This allows asters to form.
E) This allows sister chromatids to form.

F) A) and D)
G) A) and C)

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