Deck 11: DNA Technology

Full screen (f)
exit full mode
Question
In Figure 11.6, the first 10 bases of the DNA strand being sequenced are: <strong>In Figure 11.6, the first 10 bases of the DNA strand being sequenced are:  </strong> A)5'-GTGAATGCGT-3'. B)5'-TACATCGTGC-3'. C)3'-GTGAATGCGT-5'. D)3'-TACATCGTGC-5'. E)3'-ACGCATTCAC-5'. <div style=padding-top: 35px>

A)5'-GTGAATGCGT-3'.
B)5'-TACATCGTGC-3'.
C)3'-GTGAATGCGT-5'.
D)3'-TACATCGTGC-5'.
E)3'-ACGCATTCAC-5'.
Use Space or
up arrow
down arrow
to flip the card.
Question
A virgin was raped in Los Angeles and became pregnant.Police investigations have identified four suspects.The woman decided to go through with the pregnancy for religious reasons.It was possible to isolate a few cells of fetal origin from the maternal blood.Enough DNA was obtained for one polymerase chain reaction (PCR).The results for one microsatellite are shown in the gel image in Figure 11.1.Lane 1 is the mother's DNA, lane 2 is the fetal DNA, and lanes 3 to 6 are the suspect's DNA.Which of the suspects remain suspects after this analysis? <strong>A virgin was raped in Los Angeles and became pregnant.Police investigations have identified four suspects.The woman decided to go through with the pregnancy for religious reasons.It was possible to isolate a few cells of fetal origin from the maternal blood.Enough DNA was obtained for one polymerase chain reaction (PCR).The results for one microsatellite are shown in the gel image in Figure 11.1.Lane 1 is the mother's DNA, lane 2 is the fetal DNA, and lanes 3 to 6 are the suspect's DNA.Which of the suspects remain suspects after this analysis?  </strong> A)3 and 5. B)3 and 4. C)6. D)5 and 6. E)4, 5, and 6. <div style=padding-top: 35px>

A)3 and 5.
B)3 and 4.
C)6.
D)5 and 6.
E)4, 5, and 6.
Question
In the following dot blot, the probe used in the upper row is for the normal sequence while the probe in the second row is for the -Phe mutation of the cystic fibrosis gene.What are the genotypes of the four people investigated? <strong>In the following dot blot, the probe used in the upper row is for the normal sequence while the probe in the second row is for the -Phe mutation of the cystic fibrosis gene.What are the genotypes of the four people investigated?  </strong> A)Normal; affected; heterozygote; normal. B)Affected; normal; heterozygote; affected. C)Normal; heterozygote; affected; normal. D)Affected; affected; heterozygote; normal. E)Heterozygote; affected; heterozygote; heterozygote. <div style=padding-top: 35px>

A)Normal; affected; heterozygote; normal.
B)Affected; normal; heterozygote; affected.
C)Normal; heterozygote; affected; normal.
D)Affected; affected; heterozygote; normal.
E)Heterozygote; affected; heterozygote; heterozygote.
Question
PCR and DNA sequencing differ in which of the following requirements?

A)DNA polymerase.
B)An oligonucleotide primer.
C)Deoxynucleoside triphosphates.
D)DNA template.
E)Dideoxynucleoside triphosphates
Question
Figure 11.5 is an image of a gel electrophoresis pattern of a microsatellite.The samples are random blood samples from New York, and alleles containing 7, 12, 20, 22, and 35 repeat units can be seen in this gel.Which fragment corresponds to the allele containing 35 repeats? <strong>Figure 11.5 is an image of a gel electrophoresis pattern of a microsatellite.The samples are random blood samples from New York, and alleles containing 7, 12, 20, 22, and 35 repeat units can be seen in this gel.Which fragment corresponds to the allele containing 35 repeats?  </strong> A)No.1. B)No.2. C)No.3. D)No.4. E)No.5. <div style=padding-top: 35px>

A)No.1.
B)No.2.
C)No.3.
D)No.4.
E)No.5.
Question
Many oncogenic mutations change the rate at which cellular genes are expressed.All of the following methods can be used to compare the gene expression profiles of cancer cells with those of the normal cells from which they are derived, except:

A)Southern blot.
B)Western blot.
C)A DNA microarray.
D)Northern blot.
E)An immunological test that uses antibodies in order to detect proteins.
Question
The binding of an oligonucleotide probe to a specific sequence of DNA is influenced by which of the following:

A)Temperature, salt concentration, nucleotide sequence, and radioactivity only.
B)Temperature, salt concentration, pH, and nucleotide sequence only.
C)Temperature, salt concentration, and nucleotide sequence only.
D)Temperature, nucleotide sequence, and pH only.
E)Temperature and nucleotide sequence only.
Question
The following Southern blot was performed to examine a mutation that is linked to a genetic disease.The blot was probed with fluorescent-labeled cDNA of the gene.What is the most likely explanation for the abnormal bands in the patient in comparison with the normal control? <strong>The following Southern blot was performed to examine a mutation that is linked to a genetic disease.The blot was probed with fluorescent-labeled cDNA of the gene.What is the most likely explanation for the abnormal bands in the patient in comparison with the normal control?  </strong> A)Faulty splicing of the messenger RNA (mRNA). B)The deletion of an entire exon. C)A single-nucleotide polymorphism. D)Duplication of at least one exon. E)The expansion of a microsatellite. <div style=padding-top: 35px>

A)Faulty splicing of the messenger RNA (mRNA).
B)The deletion of an entire exon.
C)A single-nucleotide polymorphism.
D)Duplication of at least one exon.
E)The expansion of a microsatellite.
Question
Lane 1 in the following Southern blot contains a sample from a normal control, and lane 2 contains a sample from a patient.The arrow indicates the location of the wells in the agarose gel used in this analysis.The probe used was a complementary DNA (cDNA).Which type of mutation is most likely, on the basis of these data? <strong>Lane 1 in the following Southern blot contains a sample from a normal control, and lane 2 contains a sample from a patient.The arrow indicates the location of the wells in the agarose gel used in this analysis.The probe used was a complementary DNA (cDNA).Which type of mutation is most likely, on the basis of these data?  </strong> A)Point mutation that changes a codon encoding glutamic acid into a stop-codon. B)Deletion of part of one exon. C)A single-nucleotide polymorphism that has eliminated a restriction site. D)Duplication of three exons. E)Deletion of the entire gene. <div style=padding-top: 35px>

A)Point mutation that changes a codon encoding glutamic acid into a stop-codon.
B)Deletion of part of one exon.
C)A single-nucleotide polymorphism that has eliminated a restriction site.
D)Duplication of three exons.
E)Deletion of the entire gene.
Question
Which of the following is the most plausible recognition site for a restriction endonuclease?

A)A A G C T T.
B)C G A A G C.
C)T G C T G C.
D)A A G G C C.
E)T A C G T A.
Question
Lane 1 in the following Southern blot contains a sample from a normal control, and lane 2 contains a sample from a patient.The probe is based on the cDNA of a gene.Which type of mutation is most likely, on the basis of these data? <strong>Lane 1 in the following Southern blot contains a sample from a normal control, and lane 2 contains a sample from a patient.The probe is based on the cDNA of a gene.Which type of mutation is most likely, on the basis of these data?  </strong> A)Point mutation changing an amino acid coding codon into a stop codon. B)Insertion of an Alu sequence. C)Duplication of three exons. D)Deletion of the entire gene. E)Deletion of part of one exon. <div style=padding-top: 35px>

A)Point mutation changing an amino acid coding codon into a stop codon.
B)Insertion of an Alu sequence.
C)Duplication of three exons.
D)Deletion of the entire gene.
E)Deletion of part of one exon.
Question
RNA interference can be used for experimental and possibly therapeutic purposes.RNA interference is triggered by:

A)Shortening of telomeres in aging cells.
B)Activation of oncogenes in malignant cells.
C)Exposure to viral spike proteins.
D)Double-stranded RNA molecules.
E)DNA-RNA hybrid molecules.
Question
The most important "selectable markers" used in recombinant DNA technology with bacteria are:

A)Self-transmissible plasmid, such as the F factor.
B)Single-stranded cloning vectors that are used for DNA sequencing.
C)Genes for integrase enzymes that are needed for the integration of recombinant DNA in the bacterial genome.
D)Bacteriophages that carry a foreign DNA.
E)Genes for antibiotic resistance that permit the selective survival of engineered bacteria.
Question
What are loxP sites, and for which purpose are they used?

A)Cleavage sites for a class of restriction endonucleases that are popular for recombinant DNA studies.
B)Recombination sites that are recognized by a Cre recombinase, used for the targeted excision of genes.
C)Integration sites for retroviral vectors that are used for targeted gene insertion.
D)Sites on RNA that are the target of a selective RNase, used to suppress the expression of genes selectively.
E)Hot spots for homologous recombination, used to introduce genes into the genome by homologous recombination.
Question
In the following family, I-2 and II-1 have died from a rare form of colon cancer that is inherited as an autosomal dominant trait.The remaining family members have undergone genotyping for a microsatellite marker close to the known gene for colon cancer susceptibility.According to this analysis, what are the genotypes of the children in the third generation (left to right; the term carrier is used for a person who has the genetic disposition but has not yet developed the disease)? <strong>In the following family, I-2 and II-1 have died from a rare form of colon cancer that is inherited as an autosomal dominant trait.The remaining family members have undergone genotyping for a microsatellite marker close to the known gene for colon cancer susceptibility.According to this analysis, what are the genotypes of the children in the third generation (left to right; the term carrier is used for a person who has the genetic disposition but has not yet developed the disease)?  </strong> A)Carrier, normal, carrier, normal. B)Carrier, normal, normal, carrier. C)Normal, carrier, normal, carrier. D)Normal, carrier, carrier, normal. E)Normal, carrier, normal, normal. <div style=padding-top: 35px>

A)Carrier, normal, carrier, normal.
B)Carrier, normal, normal, carrier.
C)Normal, carrier, normal, carrier.
D)Normal, carrier, carrier, normal.
E)Normal, carrier, normal, normal.
Unlock Deck
Sign up to unlock the cards in this deck!
Unlock Deck
Unlock Deck
1/15
auto play flashcards
Play
simple tutorial
Full screen (f)
exit full mode
Deck 11: DNA Technology
1
In Figure 11.6, the first 10 bases of the DNA strand being sequenced are: <strong>In Figure 11.6, the first 10 bases of the DNA strand being sequenced are:  </strong> A)5'-GTGAATGCGT-3'. B)5'-TACATCGTGC-3'. C)3'-GTGAATGCGT-5'. D)3'-TACATCGTGC-5'. E)3'-ACGCATTCAC-5'.

A)5'-GTGAATGCGT-3'.
B)5'-TACATCGTGC-3'.
C)3'-GTGAATGCGT-5'.
D)3'-TACATCGTGC-5'.
E)3'-ACGCATTCAC-5'.
5'-GTGAATGCGT-3'.
2
A virgin was raped in Los Angeles and became pregnant.Police investigations have identified four suspects.The woman decided to go through with the pregnancy for religious reasons.It was possible to isolate a few cells of fetal origin from the maternal blood.Enough DNA was obtained for one polymerase chain reaction (PCR).The results for one microsatellite are shown in the gel image in Figure 11.1.Lane 1 is the mother's DNA, lane 2 is the fetal DNA, and lanes 3 to 6 are the suspect's DNA.Which of the suspects remain suspects after this analysis? <strong>A virgin was raped in Los Angeles and became pregnant.Police investigations have identified four suspects.The woman decided to go through with the pregnancy for religious reasons.It was possible to isolate a few cells of fetal origin from the maternal blood.Enough DNA was obtained for one polymerase chain reaction (PCR).The results for one microsatellite are shown in the gel image in Figure 11.1.Lane 1 is the mother's DNA, lane 2 is the fetal DNA, and lanes 3 to 6 are the suspect's DNA.Which of the suspects remain suspects after this analysis?  </strong> A)3 and 5. B)3 and 4. C)6. D)5 and 6. E)4, 5, and 6.

A)3 and 5.
B)3 and 4.
C)6.
D)5 and 6.
E)4, 5, and 6.
4, 5, and 6.
3
In the following dot blot, the probe used in the upper row is for the normal sequence while the probe in the second row is for the -Phe mutation of the cystic fibrosis gene.What are the genotypes of the four people investigated? <strong>In the following dot blot, the probe used in the upper row is for the normal sequence while the probe in the second row is for the -Phe mutation of the cystic fibrosis gene.What are the genotypes of the four people investigated?  </strong> A)Normal; affected; heterozygote; normal. B)Affected; normal; heterozygote; affected. C)Normal; heterozygote; affected; normal. D)Affected; affected; heterozygote; normal. E)Heterozygote; affected; heterozygote; heterozygote.

A)Normal; affected; heterozygote; normal.
B)Affected; normal; heterozygote; affected.
C)Normal; heterozygote; affected; normal.
D)Affected; affected; heterozygote; normal.
E)Heterozygote; affected; heterozygote; heterozygote.
Normal; affected; heterozygote; normal.
4
PCR and DNA sequencing differ in which of the following requirements?

A)DNA polymerase.
B)An oligonucleotide primer.
C)Deoxynucleoside triphosphates.
D)DNA template.
E)Dideoxynucleoside triphosphates
Unlock Deck
Unlock for access to all 15 flashcards in this deck.
Unlock Deck
k this deck
5
Figure 11.5 is an image of a gel electrophoresis pattern of a microsatellite.The samples are random blood samples from New York, and alleles containing 7, 12, 20, 22, and 35 repeat units can be seen in this gel.Which fragment corresponds to the allele containing 35 repeats? <strong>Figure 11.5 is an image of a gel electrophoresis pattern of a microsatellite.The samples are random blood samples from New York, and alleles containing 7, 12, 20, 22, and 35 repeat units can be seen in this gel.Which fragment corresponds to the allele containing 35 repeats?  </strong> A)No.1. B)No.2. C)No.3. D)No.4. E)No.5.

A)No.1.
B)No.2.
C)No.3.
D)No.4.
E)No.5.
Unlock Deck
Unlock for access to all 15 flashcards in this deck.
Unlock Deck
k this deck
6
Many oncogenic mutations change the rate at which cellular genes are expressed.All of the following methods can be used to compare the gene expression profiles of cancer cells with those of the normal cells from which they are derived, except:

A)Southern blot.
B)Western blot.
C)A DNA microarray.
D)Northern blot.
E)An immunological test that uses antibodies in order to detect proteins.
Unlock Deck
Unlock for access to all 15 flashcards in this deck.
Unlock Deck
k this deck
7
The binding of an oligonucleotide probe to a specific sequence of DNA is influenced by which of the following:

A)Temperature, salt concentration, nucleotide sequence, and radioactivity only.
B)Temperature, salt concentration, pH, and nucleotide sequence only.
C)Temperature, salt concentration, and nucleotide sequence only.
D)Temperature, nucleotide sequence, and pH only.
E)Temperature and nucleotide sequence only.
Unlock Deck
Unlock for access to all 15 flashcards in this deck.
Unlock Deck
k this deck
8
The following Southern blot was performed to examine a mutation that is linked to a genetic disease.The blot was probed with fluorescent-labeled cDNA of the gene.What is the most likely explanation for the abnormal bands in the patient in comparison with the normal control? <strong>The following Southern blot was performed to examine a mutation that is linked to a genetic disease.The blot was probed with fluorescent-labeled cDNA of the gene.What is the most likely explanation for the abnormal bands in the patient in comparison with the normal control?  </strong> A)Faulty splicing of the messenger RNA (mRNA). B)The deletion of an entire exon. C)A single-nucleotide polymorphism. D)Duplication of at least one exon. E)The expansion of a microsatellite.

A)Faulty splicing of the messenger RNA (mRNA).
B)The deletion of an entire exon.
C)A single-nucleotide polymorphism.
D)Duplication of at least one exon.
E)The expansion of a microsatellite.
Unlock Deck
Unlock for access to all 15 flashcards in this deck.
Unlock Deck
k this deck
9
Lane 1 in the following Southern blot contains a sample from a normal control, and lane 2 contains a sample from a patient.The arrow indicates the location of the wells in the agarose gel used in this analysis.The probe used was a complementary DNA (cDNA).Which type of mutation is most likely, on the basis of these data? <strong>Lane 1 in the following Southern blot contains a sample from a normal control, and lane 2 contains a sample from a patient.The arrow indicates the location of the wells in the agarose gel used in this analysis.The probe used was a complementary DNA (cDNA).Which type of mutation is most likely, on the basis of these data?  </strong> A)Point mutation that changes a codon encoding glutamic acid into a stop-codon. B)Deletion of part of one exon. C)A single-nucleotide polymorphism that has eliminated a restriction site. D)Duplication of three exons. E)Deletion of the entire gene.

A)Point mutation that changes a codon encoding glutamic acid into a stop-codon.
B)Deletion of part of one exon.
C)A single-nucleotide polymorphism that has eliminated a restriction site.
D)Duplication of three exons.
E)Deletion of the entire gene.
Unlock Deck
Unlock for access to all 15 flashcards in this deck.
Unlock Deck
k this deck
10
Which of the following is the most plausible recognition site for a restriction endonuclease?

A)A A G C T T.
B)C G A A G C.
C)T G C T G C.
D)A A G G C C.
E)T A C G T A.
Unlock Deck
Unlock for access to all 15 flashcards in this deck.
Unlock Deck
k this deck
11
Lane 1 in the following Southern blot contains a sample from a normal control, and lane 2 contains a sample from a patient.The probe is based on the cDNA of a gene.Which type of mutation is most likely, on the basis of these data? <strong>Lane 1 in the following Southern blot contains a sample from a normal control, and lane 2 contains a sample from a patient.The probe is based on the cDNA of a gene.Which type of mutation is most likely, on the basis of these data?  </strong> A)Point mutation changing an amino acid coding codon into a stop codon. B)Insertion of an Alu sequence. C)Duplication of three exons. D)Deletion of the entire gene. E)Deletion of part of one exon.

A)Point mutation changing an amino acid coding codon into a stop codon.
B)Insertion of an Alu sequence.
C)Duplication of three exons.
D)Deletion of the entire gene.
E)Deletion of part of one exon.
Unlock Deck
Unlock for access to all 15 flashcards in this deck.
Unlock Deck
k this deck
12
RNA interference can be used for experimental and possibly therapeutic purposes.RNA interference is triggered by:

A)Shortening of telomeres in aging cells.
B)Activation of oncogenes in malignant cells.
C)Exposure to viral spike proteins.
D)Double-stranded RNA molecules.
E)DNA-RNA hybrid molecules.
Unlock Deck
Unlock for access to all 15 flashcards in this deck.
Unlock Deck
k this deck
13
The most important "selectable markers" used in recombinant DNA technology with bacteria are:

A)Self-transmissible plasmid, such as the F factor.
B)Single-stranded cloning vectors that are used for DNA sequencing.
C)Genes for integrase enzymes that are needed for the integration of recombinant DNA in the bacterial genome.
D)Bacteriophages that carry a foreign DNA.
E)Genes for antibiotic resistance that permit the selective survival of engineered bacteria.
Unlock Deck
Unlock for access to all 15 flashcards in this deck.
Unlock Deck
k this deck
14
What are loxP sites, and for which purpose are they used?

A)Cleavage sites for a class of restriction endonucleases that are popular for recombinant DNA studies.
B)Recombination sites that are recognized by a Cre recombinase, used for the targeted excision of genes.
C)Integration sites for retroviral vectors that are used for targeted gene insertion.
D)Sites on RNA that are the target of a selective RNase, used to suppress the expression of genes selectively.
E)Hot spots for homologous recombination, used to introduce genes into the genome by homologous recombination.
Unlock Deck
Unlock for access to all 15 flashcards in this deck.
Unlock Deck
k this deck
15
In the following family, I-2 and II-1 have died from a rare form of colon cancer that is inherited as an autosomal dominant trait.The remaining family members have undergone genotyping for a microsatellite marker close to the known gene for colon cancer susceptibility.According to this analysis, what are the genotypes of the children in the third generation (left to right; the term carrier is used for a person who has the genetic disposition but has not yet developed the disease)? <strong>In the following family, I-2 and II-1 have died from a rare form of colon cancer that is inherited as an autosomal dominant trait.The remaining family members have undergone genotyping for a microsatellite marker close to the known gene for colon cancer susceptibility.According to this analysis, what are the genotypes of the children in the third generation (left to right; the term carrier is used for a person who has the genetic disposition but has not yet developed the disease)?  </strong> A)Carrier, normal, carrier, normal. B)Carrier, normal, normal, carrier. C)Normal, carrier, normal, carrier. D)Normal, carrier, carrier, normal. E)Normal, carrier, normal, normal.

A)Carrier, normal, carrier, normal.
B)Carrier, normal, normal, carrier.
C)Normal, carrier, normal, carrier.
D)Normal, carrier, carrier, normal.
E)Normal, carrier, normal, normal.
Unlock Deck
Unlock for access to all 15 flashcards in this deck.
Unlock Deck
k this deck
locked card icon
Unlock Deck
Unlock for access to all 15 flashcards in this deck.