Deck 7: Dna Mutation, DNA Repair, and Transposable Elements

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Question
Which of the following transposable elements are found in eukaryotes but not in prokaryotes?

A)IS elements
B)Families of autonomous and nonautonomous elements
C)Retrotransposons
D)Ty elements
E)B,C,and D only
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Question
A mutation during DNA replication causes a G to be inserted after the first base of the codon for tryptophan.How will this affect the growing polypeptide chain?

A)It will not be affected.
B)Elongation will stop prematurely.
C)There will be a single amino acid substitution.
D)The reading frame will be shifted to the left,and the wrong amino acids will be added from this point on.
E)An extra amino acid will be added,but the reading frame will not be affected.
Question
Nonsense suppressors are usually mutations in genes coding for

A)proteins.
B)enzymes.
C)mRNA.
D)tRNA.
E)rRNA.
Question
In order for the dissociation element (Ds)mutations in corn to be stable,

A)an Ac element must be present.
B)an Ac element must not be present.
C)the Ds must contain the gene for transposition.
D)the DNA must not be replicated.
E)None of these
Question
Which procedure would you use to detect a nutritional mutation in microorganisms?

A)Visible inspection
B)Replica plating
C)Controlled crosses
D)Isolation at high temperature
E)Plating on antibiotic-containing medium
Question
Xeroderma pigmentosum is a human genetic disease caused by

A)elevated levels of cholesterol in the blood.
B)failure to produce pigment that protects the skin cells from UV light exposure.
C)defective DNA excision-repair mechanisms.
D)mutations that inactivate tumor suppressor genes.
E)loss of genes controlling the SOS response.
Question
In Drosophila,the wild-type eye color is red.A mutation,vermilion,causes vermilion-colored eyes,unless there is a mutation in another gene,suv,which,when homozygous or hemizygous,results in eyes that are the wild-type red even in the presence of the vermilion mutation.This is an example of

A)forward mutation.
B)reverse mutation.
C)intragenic suppression.
D)intergenic suppression.
E)back mutation.
Question
Base analogs may cause mutations because

A)they modify the chemical structure and properties of the normal base.
B)they insert themselves between adjacent bases on the DNA strand and cause an extra base to be inserted during replication.
C)they remove amino groups from bases,causing them to pair with the wrong base during replication.
D)they may exist in alternate chemical states that pair with different DNA bases than the normal state during replication.
E)Both A and C
Question
Spontaneous mutation rates are greatly reduced by

A)exposure to ionizing radiation.
B)reverse mutations.
C)base-modifying agents.
D)DNA repair mechanisms.
E)performing the Ames test.
Question
A transposon is

A)a DNA segment that can insert itself at one or more sites in a genome.
B)a "jumping gene."
C)a DNA segment that may cause mutations in genes or chromosomal rearrangements.
D)a mobile genetic element that may or may not leave a copy of itself in its original site when it moves to a new site.
E)All of these
Question
Which of the following is not mutagenic?

A)5BU
B)AZT
C)Nitrous acid
D)Hydroxylamine
E)Acridine
Question
What is conservative transposition?

A)No net increase in the number of transposable elements in the genome.
B)A net increase in the number of transposable elements in the genome.
C)Movement of transposable elements with replication of the element.
D)Movement of transposable elements without replication of the element.
E)Transposition without disruption of normal gene product activity.
Question
Thymine dimers are commonly caused by

A)ultraviolet radiation.
B)ionizing radiation such as X-rays.
C)tautomers.
D)alkylating agents.
E)intercalating agents.
Question
The deamination of cytosine creates

A)5-methyl cytosine.
B)uracil.
C)2-aminopurine.
D)5-bromouracil.
E)thymine.
Question
An IS (insertion sequence)element contains

A)a transposase gene only.
B)a transposase gene and additional genes.
C)a transposase gene and inverted repeats at the ends.
D)a transposase gene,additional genes,and inverted repeats at the ends.
E)genes but not a transposase gene.
Question
Dissociation elements (Ds)in plants are examples of

A)activator transposons that can direct their own transposition.
B)nonautonomous elements that require activation by an autonomous element.
C)mutator genes that increase the spontaneous mutation frequencies of other genes.
D)repeated sequences that are targeted by a transposase.
E)Both B and C
Question
Which of the following nucleotide changes leads to a transition mutation?

A)Adenine to guanine
B)Adenine to cytosine
C)Guanine to cytosine
D)Thymine to guanine
E)Guanine to thymine
Question
Mutation frequency is the

A)number of mutations per gene per generation.
B)number of mutations per nucleotide per generation.
C)number of mutations per cell per generation.
D)number of a specific mutation in a defined population.
E)total number of mutations in a defined population.
Question
The codon 5'-AAA-3' codes for the amino acid lysine.Which of the following mutations in this codon is a neutral mutation?

A)5'-ATA-3' to isoleucine
B)5'-AGA-3' to arginine
C)5'-AAG-3' to lysine
D)5'-CAA-3' to glutamine
E)5'-AAC-3' to asparagine
Question
What kind of mutation-detection procedure can be used to detect the white-eye mutation in Drosophila?
Question
How can PCR be used to induce site-specific mutations in DNA?
Question
Composite transposons contain a central region with genes and repeated sequences at their ends but do not terminate with IS elements.
Question
Genetic manipulation in Drosophila may be assisted by the use of

A)P elements.
B)Ty elements.
C)factor.
D)bacteriophage Mu.
E)Tn10.
Question
A cointegrate is characteristic of replicative transposition.
Question
Changes in heritable traits result from adaptation to environmental influences.
Question
A tumor suppressor gene is cloned and mutagenized in vitro,then injected into mouse embryos to create knockout mice.How could you identify the heterozygous knockout mice and create mice susceptible to tumors?
Question
A transposon may carry genes for proteins that enable their transposition as well as genes for other functions such as drug resistance.
Question
An mRNA codon reads GUA.If a transition mutation occurs at the third base pair,will the final protein be changed?
Question
Somatic mutations may be inherited by the next generation.
Question
How does an intercalating agent such as ethidium bromide cause mutations?
Question
LINEs and SINEs are repetitive sequences in humans that can also,as retrotransposons,insert into genes and cause disease.
Question
A silent mutation is a change in the DNA sequence that alters the amino acid sequence of the encoded protein but does not change its function.
Question
A point mutation changes a codon from UCG to UAG.What will happen to the resulting polypeptide?
Question
5-bromouracil (5BU)is a mutagen because it is an analog of the base thymine and may pair with guanine instead of adenine if it is incorporated into a DNA strand.
Question
The DNA polymerase proofreading mechanism maintains a low mutation rate in eukaryotic genes.
Question
What are two ways that a reverse mutation can occur?
Question
A tautomer is an uncommon form of DNA base that naturally exists along with the common form.
Question
Describe how the Ames test is used to determine whether a particular chemical is mutagenic.
Question
For a particular gene,if one gene in a million experiences a mutation each generation,what is its mutation frequency?
Question
Explain how IS elements produce target-site duplications when they move.
Question
What is a retrotransposon,and how does it differ from typical transposons?
Question
Barbara McClintock discovered that a controlling element was responsible for the mutant-spotted phenotype (purple spots on white)in corn kernels.Explain how this works.
Question
How was the adaptive method for acquiring mutations disproved?
Question
Explain what a mutator gene is and give an example.
Question
How does the nucleotide excision repair (NER)system in E.coli work,and what kinds of DNA damage does it repair?
Question
Match between columns
Missense mutation
A mutation that changes a codon from one that represents an amino acid to one that signals a chain termination
Missense mutation
A mutation that changes a codon from one amino acid to another
Missense mutation
A mutation that causes an addition or deletion of one or two base pairs in a gene
Missense mutation
A mutation that causes a change in a single base pair
Missense mutation
A mutation in a gene that causes no detectable change in the protein product
Neutral mutation
A mutation that changes a codon from one that represents an amino acid to one that signals a chain termination
Neutral mutation
A mutation that changes a codon from one amino acid to another
Neutral mutation
A mutation that causes an addition or deletion of one or two base pairs in a gene
Neutral mutation
A mutation that causes a change in a single base pair
Neutral mutation
A mutation in a gene that causes no detectable change in the protein product
Point mutation
A mutation that changes a codon from one that represents an amino acid to one that signals a chain termination
Point mutation
A mutation that changes a codon from one amino acid to another
Point mutation
A mutation that causes an addition or deletion of one or two base pairs in a gene
Point mutation
A mutation that causes a change in a single base pair
Point mutation
A mutation in a gene that causes no detectable change in the protein product
Frameshift mutation
A mutation that changes a codon from one that represents an amino acid to one that signals a chain termination
Frameshift mutation
A mutation that changes a codon from one amino acid to another
Frameshift mutation
A mutation that causes an addition or deletion of one or two base pairs in a gene
Frameshift mutation
A mutation that causes a change in a single base pair
Frameshift mutation
A mutation in a gene that causes no detectable change in the protein product
Nonsense mutation
A mutation that changes a codon from one that represents an amino acid to one that signals a chain termination
Nonsense mutation
A mutation that changes a codon from one amino acid to another
Nonsense mutation
A mutation that causes an addition or deletion of one or two base pairs in a gene
Nonsense mutation
A mutation that causes a change in a single base pair
Nonsense mutation
A mutation in a gene that causes no detectable change in the protein product
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Deck 7: Dna Mutation, DNA Repair, and Transposable Elements
1
Which of the following transposable elements are found in eukaryotes but not in prokaryotes?

A)IS elements
B)Families of autonomous and nonautonomous elements
C)Retrotransposons
D)Ty elements
E)B,C,and D only
E
2
A mutation during DNA replication causes a G to be inserted after the first base of the codon for tryptophan.How will this affect the growing polypeptide chain?

A)It will not be affected.
B)Elongation will stop prematurely.
C)There will be a single amino acid substitution.
D)The reading frame will be shifted to the left,and the wrong amino acids will be added from this point on.
E)An extra amino acid will be added,but the reading frame will not be affected.
D
3
Nonsense suppressors are usually mutations in genes coding for

A)proteins.
B)enzymes.
C)mRNA.
D)tRNA.
E)rRNA.
D
4
In order for the dissociation element (Ds)mutations in corn to be stable,

A)an Ac element must be present.
B)an Ac element must not be present.
C)the Ds must contain the gene for transposition.
D)the DNA must not be replicated.
E)None of these
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Unlock for access to all 46 flashcards in this deck.
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5
Which procedure would you use to detect a nutritional mutation in microorganisms?

A)Visible inspection
B)Replica plating
C)Controlled crosses
D)Isolation at high temperature
E)Plating on antibiotic-containing medium
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Unlock for access to all 46 flashcards in this deck.
Unlock Deck
k this deck
6
Xeroderma pigmentosum is a human genetic disease caused by

A)elevated levels of cholesterol in the blood.
B)failure to produce pigment that protects the skin cells from UV light exposure.
C)defective DNA excision-repair mechanisms.
D)mutations that inactivate tumor suppressor genes.
E)loss of genes controlling the SOS response.
Unlock Deck
Unlock for access to all 46 flashcards in this deck.
Unlock Deck
k this deck
7
In Drosophila,the wild-type eye color is red.A mutation,vermilion,causes vermilion-colored eyes,unless there is a mutation in another gene,suv,which,when homozygous or hemizygous,results in eyes that are the wild-type red even in the presence of the vermilion mutation.This is an example of

A)forward mutation.
B)reverse mutation.
C)intragenic suppression.
D)intergenic suppression.
E)back mutation.
Unlock Deck
Unlock for access to all 46 flashcards in this deck.
Unlock Deck
k this deck
8
Base analogs may cause mutations because

A)they modify the chemical structure and properties of the normal base.
B)they insert themselves between adjacent bases on the DNA strand and cause an extra base to be inserted during replication.
C)they remove amino groups from bases,causing them to pair with the wrong base during replication.
D)they may exist in alternate chemical states that pair with different DNA bases than the normal state during replication.
E)Both A and C
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Unlock for access to all 46 flashcards in this deck.
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k this deck
9
Spontaneous mutation rates are greatly reduced by

A)exposure to ionizing radiation.
B)reverse mutations.
C)base-modifying agents.
D)DNA repair mechanisms.
E)performing the Ames test.
Unlock Deck
Unlock for access to all 46 flashcards in this deck.
Unlock Deck
k this deck
10
A transposon is

A)a DNA segment that can insert itself at one or more sites in a genome.
B)a "jumping gene."
C)a DNA segment that may cause mutations in genes or chromosomal rearrangements.
D)a mobile genetic element that may or may not leave a copy of itself in its original site when it moves to a new site.
E)All of these
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11
Which of the following is not mutagenic?

A)5BU
B)AZT
C)Nitrous acid
D)Hydroxylamine
E)Acridine
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k this deck
12
What is conservative transposition?

A)No net increase in the number of transposable elements in the genome.
B)A net increase in the number of transposable elements in the genome.
C)Movement of transposable elements with replication of the element.
D)Movement of transposable elements without replication of the element.
E)Transposition without disruption of normal gene product activity.
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13
Thymine dimers are commonly caused by

A)ultraviolet radiation.
B)ionizing radiation such as X-rays.
C)tautomers.
D)alkylating agents.
E)intercalating agents.
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k this deck
14
The deamination of cytosine creates

A)5-methyl cytosine.
B)uracil.
C)2-aminopurine.
D)5-bromouracil.
E)thymine.
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k this deck
15
An IS (insertion sequence)element contains

A)a transposase gene only.
B)a transposase gene and additional genes.
C)a transposase gene and inverted repeats at the ends.
D)a transposase gene,additional genes,and inverted repeats at the ends.
E)genes but not a transposase gene.
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k this deck
16
Dissociation elements (Ds)in plants are examples of

A)activator transposons that can direct their own transposition.
B)nonautonomous elements that require activation by an autonomous element.
C)mutator genes that increase the spontaneous mutation frequencies of other genes.
D)repeated sequences that are targeted by a transposase.
E)Both B and C
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Unlock for access to all 46 flashcards in this deck.
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k this deck
17
Which of the following nucleotide changes leads to a transition mutation?

A)Adenine to guanine
B)Adenine to cytosine
C)Guanine to cytosine
D)Thymine to guanine
E)Guanine to thymine
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k this deck
18
Mutation frequency is the

A)number of mutations per gene per generation.
B)number of mutations per nucleotide per generation.
C)number of mutations per cell per generation.
D)number of a specific mutation in a defined population.
E)total number of mutations in a defined population.
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Unlock Deck
k this deck
19
The codon 5'-AAA-3' codes for the amino acid lysine.Which of the following mutations in this codon is a neutral mutation?

A)5'-ATA-3' to isoleucine
B)5'-AGA-3' to arginine
C)5'-AAG-3' to lysine
D)5'-CAA-3' to glutamine
E)5'-AAC-3' to asparagine
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20
What kind of mutation-detection procedure can be used to detect the white-eye mutation in Drosophila?
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k this deck
21
How can PCR be used to induce site-specific mutations in DNA?
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22
Composite transposons contain a central region with genes and repeated sequences at their ends but do not terminate with IS elements.
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Unlock Deck
k this deck
23
Genetic manipulation in Drosophila may be assisted by the use of

A)P elements.
B)Ty elements.
C)factor.
D)bacteriophage Mu.
E)Tn10.
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k this deck
24
A cointegrate is characteristic of replicative transposition.
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k this deck
25
Changes in heritable traits result from adaptation to environmental influences.
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k this deck
26
A tumor suppressor gene is cloned and mutagenized in vitro,then injected into mouse embryos to create knockout mice.How could you identify the heterozygous knockout mice and create mice susceptible to tumors?
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k this deck
27
A transposon may carry genes for proteins that enable their transposition as well as genes for other functions such as drug resistance.
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k this deck
28
An mRNA codon reads GUA.If a transition mutation occurs at the third base pair,will the final protein be changed?
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29
Somatic mutations may be inherited by the next generation.
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30
How does an intercalating agent such as ethidium bromide cause mutations?
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31
LINEs and SINEs are repetitive sequences in humans that can also,as retrotransposons,insert into genes and cause disease.
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k this deck
32
A silent mutation is a change in the DNA sequence that alters the amino acid sequence of the encoded protein but does not change its function.
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33
A point mutation changes a codon from UCG to UAG.What will happen to the resulting polypeptide?
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34
5-bromouracil (5BU)is a mutagen because it is an analog of the base thymine and may pair with guanine instead of adenine if it is incorporated into a DNA strand.
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35
The DNA polymerase proofreading mechanism maintains a low mutation rate in eukaryotic genes.
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k this deck
36
What are two ways that a reverse mutation can occur?
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37
A tautomer is an uncommon form of DNA base that naturally exists along with the common form.
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38
Describe how the Ames test is used to determine whether a particular chemical is mutagenic.
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39
For a particular gene,if one gene in a million experiences a mutation each generation,what is its mutation frequency?
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40
Explain how IS elements produce target-site duplications when they move.
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41
What is a retrotransposon,and how does it differ from typical transposons?
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42
Barbara McClintock discovered that a controlling element was responsible for the mutant-spotted phenotype (purple spots on white)in corn kernels.Explain how this works.
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43
How was the adaptive method for acquiring mutations disproved?
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44
Explain what a mutator gene is and give an example.
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45
How does the nucleotide excision repair (NER)system in E.coli work,and what kinds of DNA damage does it repair?
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46
Match between columns
Missense mutation
A mutation that changes a codon from one that represents an amino acid to one that signals a chain termination
Missense mutation
A mutation that changes a codon from one amino acid to another
Missense mutation
A mutation that causes an addition or deletion of one or two base pairs in a gene
Missense mutation
A mutation that causes a change in a single base pair
Missense mutation
A mutation in a gene that causes no detectable change in the protein product
Neutral mutation
A mutation that changes a codon from one that represents an amino acid to one that signals a chain termination
Neutral mutation
A mutation that changes a codon from one amino acid to another
Neutral mutation
A mutation that causes an addition or deletion of one or two base pairs in a gene
Neutral mutation
A mutation that causes a change in a single base pair
Neutral mutation
A mutation in a gene that causes no detectable change in the protein product
Point mutation
A mutation that changes a codon from one that represents an amino acid to one that signals a chain termination
Point mutation
A mutation that changes a codon from one amino acid to another
Point mutation
A mutation that causes an addition or deletion of one or two base pairs in a gene
Point mutation
A mutation that causes a change in a single base pair
Point mutation
A mutation in a gene that causes no detectable change in the protein product
Frameshift mutation
A mutation that changes a codon from one that represents an amino acid to one that signals a chain termination
Frameshift mutation
A mutation that changes a codon from one amino acid to another
Frameshift mutation
A mutation that causes an addition or deletion of one or two base pairs in a gene
Frameshift mutation
A mutation that causes a change in a single base pair
Frameshift mutation
A mutation in a gene that causes no detectable change in the protein product
Nonsense mutation
A mutation that changes a codon from one that represents an amino acid to one that signals a chain termination
Nonsense mutation
A mutation that changes a codon from one amino acid to another
Nonsense mutation
A mutation that causes an addition or deletion of one or two base pairs in a gene
Nonsense mutation
A mutation that causes a change in a single base pair
Nonsense mutation
A mutation in a gene that causes no detectable change in the protein product
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