homework chp. 11 Flashcards

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1
Q

The purpose of the Ames Test is to​ _______.
a. determine whether histidine has mutagenic effects in S. typhimurium
b. test the mutagenic effects of chemicals
c. determine whether Salmonella d. typhimurium​ his- mutants can revert to ​his+
d. study how the liver affects potential mutagens

A

b. test the mutagenic effects of chemicals

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2
Q

In the Ames​ Test, the appearance of his​+ revertants in the presence of a​ non-mutagenic control compound indicates that​ _______.
a. there is some​ low-level contamination in most experiments
b. some of the reversion mutations are not caused by the mutagen being tested
d. the growth medium contains factors that are mildly mutagenic
e. liver extract increases the potency of some mutagens

A

some of the reversion mutations are not caused by the mutagen being tested

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3
Q

Many chemicals are more mutagenic after being processed in the liver.
a. True
b. False

A

true

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4
Q

All compounds that have been found to be mutagenic in the Ames test are also carcinogenic.

A

false

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5
Q

Why are liver extracts used in the Ames​ test?
a. A liver extract is necessary for the bacteria to produce histidine revertants.
b. The bacteria require the nutrients present in the liver extract for growth.
c. Liver enzymes activate the bacterial enzymes.
d. Liver enzymes may activate some innocuous​ compounds, making them mutagenic.

A

Liver enzymes may activate some innocuous​ compounds, making them mutagenic.

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6
Q

Which bacteria grow on the agar plate if the Ames test is​ positive?

A

his​+ prototrophs

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7
Q

To use RFLP analysis to detect a​ SNP, the SNP must​ _______.
a. be present in at least​ 1% of the population
b. occur in homozygous form
c. cause disease
d. occur within a restriction enzyme recognition sequence

A

occur within a restriction enzyme recognition sequence

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8
Q

One advantage of​ allele-specific oligonucleotide​ (ASO)-based over​ RFLP-based detection of human genetic disease is that​ _______.
​a. ASO-based methods can identify heterozygotes as well as homozygotes
​b. RFLP-based methods require electrophoresis
​c. ASO-based methods can detect mutations as small as a single nucleotide
d. the mutation need not be located within a restriction enzyme recognition site

A

the mutation need not be located within a restriction enzyme recognition site

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9
Q

Molecular tests for​ Huntington’s disease, cystic​ fibrosis, and​ Tay-Sachs disease are possible because​ _______.
a. there has been sufficient information gathered on the DNA sequences of both b. the mutant and normal alleles
these diseases occur in greater than​ 1% of the population
c. the symptoms of these diseases are well documented
d. the chromosome on which each gene is located is known

A

there has been sufficient information gathered on the DNA sequences of both the mutant and normal alleles

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10
Q

In terms of its involvement in​ mutagenesis, 5BU is best described as​ _______.
a. a chemical that alters the structure of nitrogenous bases
b. a base analog that can cause either​ A-T >​ G-C or​ G-C >​ A-T transitions
Your answer is correct.
c. a rare form of adenine that can base pair with cytosine
d. a base analog​ that, if incorporated into a DNA molecule during​ replication, remains permanently in its rare form

A

a base analog that can cause either​ A-T >​ G-C or​ G-C >​ A-T transitions

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11
Q

For 5BU to cause a transition​ mutation, which of the following must​ occur?
a. It must be incorporated into DNA in its rare form.
b. It must undergo at least two form changes.
c. DNA with incorporated 5BU must replicate.
d. DNA with incorporated 5BU must not replicate.

A

DNA with incorporated 5BU must replicate.

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12
Q

In its rare​ form, 5BU pairs with guanine.
a. True
b. False

A

true

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13
Q

What are the consequences of having pyrimidine dimers in​ DNA?
a. They form an extra phosphodiester bond between them.
b. These dimers distort the DNA structure and result in errors during DNA replication.
c. They create an apyrimidinic site
d. They prevent the transcription of the DNA into RNA.

A

These dimers distort the DNA structure and result in errors during DNA replication.

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14
Q

Thymine dimers can be repaired by Photoreactivation Repair or Nucleotide Excision Repair.
a. true
b. false

A

true

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15
Q

Which of the following statements regarding Nucleotide Excision Repair​ (NER) and Base Excision Repair​ (BER) is​ true?
a. Only NER involves the action of DNA ligase to seal nicks in the DNA backbone.
b. Both NER and BER can be activated by exposure to visible light.
c. Both NER and BER involve the creation of an apyrimidinic​ (AP) site.
d. Both NER and BER involve the removal of one or more damaged bases by a nuclease.

A

Both NER and BER involve the removal of one or more damaged bases by a nuclease.

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16
Q

Which structures can be involved in​ recombination?
a. Chromatids of homologous chromosomes
b. Chromosomes in different cells
c. Any two chromosomes
d. Chromatids of nonhomologous chromosomes

A

Chromatids of homologous chromosomes

17
Q

cThe process that determines the length of heteroduplex DNA on the chromatids is called branch migration.

A

true

18
Q

Which process does not occur during​ recombination?
a. Ligation
b. DNA polymerization
c. Strand displacement
d. Nicking of the​ sugar‑phosphate backbone

A

b. DNA polymerization

19
Q

All of the following are characteristics of insertion sequences elements except​ _______.
a. they encode protein
b. they are flanked by inverted repeats
c. a copy of the insertion sequence becomes integrated at a new location
d. there can be more than one copy of an IS element in a bacterial genome

A

cutting DNA at the target sequence

20
Q

Which of the following transposition events is most likely to result in a loss of function​ mutation?
a. Insertion near the promoter region of a gene
b. Transposition of an IS element that contains a stop codon within the inverted repeat sequence
c. Insertion of an IS element within the coding region of a gene

A

Insertion of an IS element within the coding region of a gene

21
Q

Which repair process in E. coli uses visible light to repair thymine​ dimers?

A

photoreactivation repair

22
Q

Which two repair processes are the most error​ prone?

A

translesion DNA synthesis (SOS repair)
non homologous end joining

23
Q

What kind of DNA lesion does UV energy​ cause?

A

pyrimidine dimerization

24
Q

The three features of genes or of DNA sequences that contribute to the occurrence of mutational hotspots were described in chapter 12 in the textbook.
what are they?

A

large genes
regions rich in CpG dinucleotides
long stretches of trinucleotide repeats

25
Q

Which of the following spontaneous mutations alters DNA​ structure/sequence and generally results from strand​ slippage? See Section 11.2.
a. Tautomeric shift that changes the structure of a base
b. Expansion of trinucleotide repeat sequences
c. Deamination of cytosine
d. Depurination

A

b. Expansion of trinucleotide repeat sequences

26
Q

A​ second-site mutation that compensates for the mutation in one gene by mutating a second gene and restoring the​ wild-type phenotype is also known as a​ ________ .
a. intragenic reversion
b. suppressor mutation
c. true reversion
d. forward mutation

A

b. suppressor mutation

27
Q

Localized mutations that occur at a specific​ location, rather than over a larger span on a gene are better known as​ what?
​a. base-pair substitution mutations
b. frameshift mutation
c. point mutations
d. adaptive mutations

A

c. point mutations

28
Q

A manufacturer of nutritional supplements proposes to sell extracts from an Antarctic algae as an ingestible remedy for sleep disorders. Your task is to determine if this extract may be​ mutagenic, how do you test​ this?
a. Ames test
b. with alkylating agents
c. with UV radiation
d. fluctuation test

A

a. Ames test

29
Q

​________ are structures that have the same composition and general arrangement but a slight difference in bonding and placement of a hydrogen.
a. Mispairs
b. Frameshifts
c. Hotspots
d. Tautomers

A

d. Tautomers

30
Q

Which type of DNA damage is repaired by the enzyme​ photolyase? See Section 11.4.
a. Apurinic sites
b. Methylated or alkylated bases
c. Thyminedimers
​d. Single-strand breaks in the DNA backbone

A

c. Thyminedimers

31
Q

Which type of mutagen has a structure similar to one of the DNA nucleotides and therefore can work its way into​ DNA, where it pairs with a​ nucleotide?
a. nucleotide base analog
b. deaminating agent
c. hydroxylating agent
d. alkylating agent

A

a. nucleotide base analog

32
Q

The role that p53 protein plays in suppressing inappropriate progression through the cell cycle depends on all of the following EXCEPT​ _______.
a. p53 indirectly blocks G1 to S transition in the cell cycle
b. p53 stability increases in the presence of unrepaired DNA lesions
c. p53 activates transcription of WAF1
c. the ability of p53 to bind DNA lesions

A

c. the ability of p53 to bind DNA lesions

33
Q

Which of the following is a consequence of inactivation of both p53 alleles in a​ cell?
a. Programmed cell death​ (apoptosis) of the cell
d. A reduction in kinase activity of the​ cyclin-Cdk complex
c. Reduction of p21 synthesis
d. Relative instability of the​ non-functional protein

A

c. Reduction of p21 synthesis

34
Q

In the presence of DNA lesions in the​ cell, the stability of p53 protein increases.
True
False

A

true