Deck 15: Gene Regulation in Prokaryotes
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Deck 15: Gene Regulation in Prokaryotes
1
The yeast Saccharomyces cerevisiae reproduces _______________,allowing easy determination of the cell-cycle stage in which a cell is found.
A) ambiguously
B) by fission
C) sexually
D) amorphously
E) by budding
A) ambiguously
B) by fission
C) sexually
D) amorphously
E) by budding
E
2
The yeast Saccharomyces cerevisiae is particularly useful for genetic analysis of cell-cycle control because
A) it is prokaryotic,allowing it to divide rapidly.
B) mutant yeast cells form cancerous tumours.
C) reproduction by budding allows easy identification of the cell-cycle stage.
D) all cells in a culture remain at the same stage of the cell cycle.
E) yeast cells lack G1 and G2 stages.
A) it is prokaryotic,allowing it to divide rapidly.
B) mutant yeast cells form cancerous tumours.
C) reproduction by budding allows easy identification of the cell-cycle stage.
D) all cells in a culture remain at the same stage of the cell cycle.
E) yeast cells lack G1 and G2 stages.
C
3
The ____________ checkpoint is disrupted by mutations that alter p53 function.
A) G0-to-G1
B) G1-to-S
C) S-to-G2
D) G2-to-M
E) M-to-G1
A) G0-to-G1
B) G1-to-S
C) S-to-G2
D) G2-to-M
E) M-to-G1
B
4
The cell-cycle checkpoint that occurs during mitosis causes nuclear division to pause until
A) DNA replication is complete.
B) sister chromatids have separated.
C) cytokinesis occurs.
D) telophase begins.
E) all chromosomes have attached to the mitotic spindle.
A) DNA replication is complete.
B) sister chromatids have separated.
C) cytokinesis occurs.
D) telophase begins.
E) all chromosomes have attached to the mitotic spindle.
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5
Enzymes that covalently link phosphate groups to their substrates are termed
A) kinases.
B) phosphatases.
C) cyclins.
D) phosphatase inhibitors.
E) ligases.
A) kinases.
B) phosphatases.
C) cyclins.
D) phosphatase inhibitors.
E) ligases.
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6
CDKs,such as CDC28,require the assistance of ____________ to carry out their enzymatic activity.
A) restriction enzymes
B) proteases
C) nucleases
D) growth factors
E) cyclins
A) restriction enzymes
B) proteases
C) nucleases
D) growth factors
E) cyclins
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7
In the cell cycle of Saccharomyces cerevisiae,the appearance of a bud on the surface of a cell indicates that the cell
A) is entering M phase.
B) has a mutation in a gene regulating G2M transition.
C) is haploid.
D) has a mutation in a gene regulating G2S transition.
E) is reaching the end of G1 phase.
A) is entering M phase.
B) has a mutation in a gene regulating G2M transition.
C) is haploid.
D) has a mutation in a gene regulating G2S transition.
E) is reaching the end of G1 phase.
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8
The temperature at which a cell with a temperature-sensitive mutation is unable to survive is considered the ___________ temperature.
A) restrictive
B) mutant
C) dissociative
D) permissive
E) alternative
A) restrictive
B) mutant
C) dissociative
D) permissive
E) alternative
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9
Which of the following does not occur during mitosis?
A) segregation of sister chromatids
B) duplication of chromosomal DNA
C) condensation of chromosomes
D) nuclear envelope breakdown
E) attachment of chromosomes to mitotic spindle
A) segregation of sister chromatids
B) duplication of chromosomal DNA
C) condensation of chromosomes
D) nuclear envelope breakdown
E) attachment of chromosomes to mitotic spindle
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10
Which of the following is not a common consequence of mutations that eliminate cell-cycle checkpoints?
A) increased DNA damage
B) decreased frequency of cell division
C) polyploidy
D) aneuploidy
E) increased chromosome loss
A) increased DNA damage
B) decreased frequency of cell division
C) polyploidy
D) aneuploidy
E) increased chromosome loss
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11
Molecules that function to stimulate or inhibit cell division are collectively referred to as
A) transcription factors.
B) polymerases.
C) kinases.
D) growth factors.
E) checkpoints.
A) transcription factors.
B) polymerases.
C) kinases.
D) growth factors.
E) checkpoints.
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12
Which of the following is not likely to result from the loss of functional p53?
A) the appearance of homogenously staining regions on chromosomes
B) increases propensity to arrest in G1
C) alterations in the G1 to S checkpoint
D) an increase in gene amplification in affected cells
E) generation of fragments of chromosomal DNA lacking telomeres and centromeres
A) the appearance of homogenously staining regions on chromosomes
B) increases propensity to arrest in G1
C) alterations in the G1 to S checkpoint
D) an increase in gene amplification in affected cells
E) generation of fragments of chromosomal DNA lacking telomeres and centromeres
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13
A programmed cell change that results in cell death is referred to as
A) apoptosis.
B) G1 regulation.
C) post-translational control.
D) cancer.
E) metastasis.
A) apoptosis.
B) G1 regulation.
C) post-translational control.
D) cancer.
E) metastasis.
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14
Damage to DNA that takes place during DNA replication results in arrest of normal cells at the _______________ checkpoint.
A) G0-to-G1
B) G1-to-S
C) S-to-G2
D) G2-to-M
E) M-to-G1
A) G0-to-G1
B) G1-to-S
C) S-to-G2
D) G2-to-M
E) M-to-G1
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15
CDKs associate with cyclins at specific stages of the cell cycle.The CDK subunit is responsible for phosphorylating a substrate protein,while the cyclin is responsible for
A) progression into G0.
B) degradation of the CDK after phosphorylation.
C) ubiquitin function.
D) dephosphorylating Rb.
E) determining which specific proteins will be phosphorylated.
A) progression into G0.
B) degradation of the CDK after phosphorylation.
C) ubiquitin function.
D) dephosphorylating Rb.
E) determining which specific proteins will be phosphorylated.
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16
________________ are proteins that form a structural scaffold on the inner surface of the nuclear membrane.
A) Mitotic tubules
B) Nuclear lamins
C) Chromatin fibrils
D) CDKs
E) Histones
A) Mitotic tubules
B) Nuclear lamins
C) Chromatin fibrils
D) CDKs
E) Histones
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17
The solubility of nuclear lamins is regulated by the _____________ of lamin proteins.
A) length
B) phosphorylation state
C) kinase activity
D) molecular weight
E) condensation
A) length
B) phosphorylation state
C) kinase activity
D) molecular weight
E) condensation
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18
The retinoblastoma (Rb)protein regulates progression into S phase by regulating ___________ activity.
A) cyclin D
B) p53
C) CDK4
D) E2F
E) CDC28
A) cyclin D
B) p53
C) CDK4
D) E2F
E) CDC28
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19
One characteristic of cancer is unregulated cell proliferation.A second characteristic of cancer cells is
A) the synthesis of additional copies of DNA polymerase.
B) arrest in G0.
C) the failure to expand clonally.
D) apoptosis.
E) the ability to migrate to distant tissues.
A) the synthesis of additional copies of DNA polymerase.
B) arrest in G0.
C) the failure to expand clonally.
D) apoptosis.
E) the ability to migrate to distant tissues.
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20
The cells in a population of yeast cells in which all members of the population have a temperature-sensitive mutation in the same gene involved in cell-cycle progression will appear _________ when shifted to the restrictive temperature.
A) to vary in morphology
B) as clumps of lysed cells
C) to adhere to each other
D) uniform in size and shape
E) arrested in all stages of the cell cycle
A) to vary in morphology
B) as clumps of lysed cells
C) to adhere to each other
D) uniform in size and shape
E) arrested in all stages of the cell cycle
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21
In Saccharomyces cerevisiae,the _________________ protein inhibits progression of the cell cycle into mitosis in response to DNA damage.
A) p53
B) RAD9
C) Rb
D) E2F
E) CDK
A) p53
B) RAD9
C) Rb
D) E2F
E) CDK
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22
______________________ are mutant forms of normal genes that act dominantly to predispose a cell to a cancerous phenotype.
A) Polymerases
B) Oncogenes
C) Activators
D) Tumour suppressors
E) Proto-oncogenes
A) Polymerases
B) Oncogenes
C) Activators
D) Tumour suppressors
E) Proto-oncogenes
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23
Genes encoding which of the following protein types do not function as oncogenes when mutated?
A) transmembrane receptors
B) transcription factors
C) signal transmitters
D) growth factors
E) tumour suppressors
A) transmembrane receptors
B) transcription factors
C) signal transmitters
D) growth factors
E) tumour suppressors
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24
Cyclin-dependent kinases require _______________________ to catalyze phosphorylation of appropriate substrate proteins.
A) cyclins
B) growth factors
C) mutagens
D) receptors
E) aneuploidy
A) cyclins
B) growth factors
C) mutagens
D) receptors
E) aneuploidy
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25
Cytoplasmic proteins that relay signals inside the cell are referred to as
A) growth factors.
B) signal transducers.
C) receptors.
D) transcription factors.
E) polymerases.
A) growth factors.
B) signal transducers.
C) receptors.
D) transcription factors.
E) polymerases.
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26
Genetic testing for cancer can
A) identify individuals that are resistant to cancer.
B) indicate increased risk of certain cancers.
C) predict the age of cancer onset in an individual.
D) eliminate the possibility that an individual will develop cancer.
E) do none of the choices.
A) identify individuals that are resistant to cancer.
B) indicate increased risk of certain cancers.
C) predict the age of cancer onset in an individual.
D) eliminate the possibility that an individual will develop cancer.
E) do none of the choices.
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27
______________________ are proteins that assist in regulating cell-cycle progression and are often rapidly degraded at specific times in the cell cycle.
A) Cyclins
B) Growth factors
C) Mutagens
D) Receptors
E) Cyclin-dependent kinases
A) Cyclins
B) Growth factors
C) Mutagens
D) Receptors
E) Cyclin-dependent kinases
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28
Genes whose mutant alleles can function in a recessive manner to predispose cells to cancerous growth are referred to as
A) polymerases.
B) oncogenes.
C) activators.
D) tumour suppressors.
E) proto-oncogenes.
A) polymerases.
B) oncogenes.
C) activators.
D) tumour suppressors.
E) proto-oncogenes.
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29
Cells that have migrated from a tumour and invaded a distant tissue are said to have
A) acclimated.
B) metastasized.
C) mutagenized.
D) carcinogenized.
E) capacitated.
A) acclimated.
B) metastasized.
C) mutagenized.
D) carcinogenized.
E) capacitated.
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30
_____________________ are enzymes that function to promote or inhibit cell cycle progression by phosphorylating specific substrates.
A) Cyclins
B) Growth factors
C) Mutagens
D) Cyclic phosphatases
E) Cyclin-dependent kinases
A) Cyclins
B) Growth factors
C) Mutagens
D) Cyclic phosphatases
E) Cyclin-dependent kinases
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31
All cells in a cancerous tumour arise from a single mutant precursor cell,meaning that the cells in the tumour are
A) sporadic.
B) spastic.
C) benign.
D) divisionary.
E) clonal.
A) sporadic.
B) spastic.
C) benign.
D) divisionary.
E) clonal.
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32
_______________________ are proteins that span the plasma membrane and transmit signals from outside the cell into the cytoplasm.
A) Receptors
B) Transcription factors
C) Growth factors
D) Nucleosomes
E) Polymerases
A) Receptors
B) Transcription factors
C) Growth factors
D) Nucleosomes
E) Polymerases
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33
Which of the following statements regarding cancer is true?
A) All cancers are genetic diseases.
B) All cancers are sporadic.
C) All cancers run in families.
D) All cancers are caused by the same mutagen.
E) All cancers are caused by the same mutations.
A) All cancers are genetic diseases.
B) All cancers are sporadic.
C) All cancers run in families.
D) All cancers are caused by the same mutagen.
E) All cancers are caused by the same mutations.
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34
Alterations in the activity of cyclin-dependent kinases can affect the _____________ cell cycle checkpoint.
A) G1-to-S
B) S-to-G2
C) G2-to-M
D) G1-to-S or G2-to-M
E) G1-to-S,S-to-G2,or G2-to-M
A) G1-to-S
B) S-to-G2
C) G2-to-M
D) G1-to-S or G2-to-M
E) G1-to-S,S-to-G2,or G2-to-M
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35
In its active form,the RAS protein is associated with
A) DNA.
B) ATP.
C) GTP.
D) RNA.
E) GDP.
A) DNA.
B) ATP.
C) GTP.
D) RNA.
E) GDP.
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36
Which of the following does not function to reduce the likelihood of a cell becoming cancerous?
A) alternative splicing within the nucleus
B) mismatch repair enzymes
C) proofreading ability of DNA polymerases
D) cell-cycle checkpoints
E) tumour-suppressor genes
A) alternative splicing within the nucleus
B) mismatch repair enzymes
C) proofreading ability of DNA polymerases
D) cell-cycle checkpoints
E) tumour-suppressor genes
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37
The human papilloma virus (HPV)carries a gene that functions as an oncogene by inactivating the p53 protein.The fact that the loss of p53 function is oncogenic suggests that
A) p53 normally functions to prevent uncontrolled cell division.
B) the HPV protein is encoded by a tumour-suppressor gene.
C) p53 gene expression is upregulated by the HPV protein.
D) the HPV protein functions at origins of replication on DNA.
E) p53 is a proto-oncogene.
A) p53 normally functions to prevent uncontrolled cell division.
B) the HPV protein is encoded by a tumour-suppressor gene.
C) p53 gene expression is upregulated by the HPV protein.
D) the HPV protein functions at origins of replication on DNA.
E) p53 is a proto-oncogene.
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38
Tumour cells removed from an individual with retinoblastoma are _________________ for a deletion of the RB gene.
A) homozygous
B) heterologous
C) hemizygous
D) heterozygous
E) endozygous
A) homozygous
B) heterologous
C) hemizygous
D) heterozygous
E) endozygous
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39
The generation of a cancerous cell requires mutations in ____________ of that cell's genes.
A) none
B) one
C) two
D) six to ten
E) more than 100
A) none
B) one
C) two
D) six to ten
E) more than 100
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40
Normal alleles of tumour-suppressor genes function to encode proteins that
A) promote transition from G1-to-S.
B) can slow the rate of cell division.
C) increase the rate of mutagenesis.
D) activate oncogenes.
E) associate with growth factors at the cell surface.
A) promote transition from G1-to-S.
B) can slow the rate of cell division.
C) increase the rate of mutagenesis.
D) activate oncogenes.
E) associate with growth factors at the cell surface.
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41
Define: Signal transduction
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42
Of the approximately 300 cell types,some,once terminally differentiated,never divide again even if life continues for nearly a century.
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43
You wish to determine which genes are aberrantly expressed in a certain type of cancer.How would you measure a possible transcription difference on a genomic level between the cancer cells and normal cells?
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44
You have identified a mutation in Gene X that appears along with mutations in three other genes to cause an increased likelihood for a certain cancer.Develop an assay to test patients for the polymorphism in Gene X.
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45
An enzyme that removes a phosphate group from proteins is called a phosphatase.
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46
The cells in a cancerous tumour are described as being "clonal." What does this mean?
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47
DNA damage in normal cells only rarely leads to apoptosis.
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48
Oncogenes found in viral genome often cause _____________________ when incorporated into eukaryotic cells.
A) cell death
B) arrest in G0
C) increased cell proliferation
D) arrest at the G2-to-M checkpoint
E) apoptosis
A) cell death
B) arrest in G0
C) increased cell proliferation
D) arrest at the G2-to-M checkpoint
E) apoptosis
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49
Name two mechanisms by which a retrovirus carrying a proto-oncogene can convert the proto-oncogene to an oncogene.
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50
Define: CDK
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51
Using yeast,you wish to test the hypothesis that two new temperature-sensitive mutations you have isolated are involved in different steps of the cell cycle.Describe the experimental setup necessary to do so.
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52
DNA damage activates the p53 transcription factor,which in turn induces expression of the p21 gene.
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53
The S phase is when sister chromosomes segregate into daughter cells.
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54
A temperature-sensitive screen is completed by treating cells with mutagen,replica plating,and then selecting for growth in permissive and restrictive temperatures.
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55
Cell-cycle check points are arrests to the cell cycle in which the integrity of the genome and cell-cycle machinery are "checked" prior to continuing to the next cell-cycle stage.
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56
Cyclin-dependent kinases together with cyclins control the timing of cell-cycle events.
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57
Define: Proto-oncogene
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58
Cell-surface receptors function to transmit signals from the outside of the cell into the cytoplasm.Name the three protein domains that are responsible for receptors to accomplish this signal transmission.
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59
Define: Apoptosis
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60
The cell cycle has four phases,G,S1,S2,and M.
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61
Define: Tumour-suppressor gene
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62
A patient presents with cancer tumours in several organs.You genotype for several genes often related to the causation of cancer and find that cells from each disparate tumour have the same genotype for all of the genes tested.How do you interpret this data?
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63
Define: RB
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64
Define: Growth factor
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65
Define: Oncogene
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