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Explain how UV light induces mutations in E. coli.

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UV light induces mutations in E. coli by...

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To determine whether human exposure to radiation results in an increase in recessive mutations in the germ line, scientists can examine the sex ratio of children born to parents exposed to higher than normal radiation levels. Explain how and why the sex ratio might be affected by radiation exposure.

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The sex ratio of children born to parent...

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How will the result of strand slippage on the newly synthesized strand differ from the result of strand slippage on the template strand?

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The result of strand slippage on the new...

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Which of the following mutagens is MOST likely to cause a frameshift mutation?


A) base analog
B) alkylating agent
C) intercalating agent
D) ionizing radiation
E) UV light

F) A) and E)
G) A) and B)

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Transposable elements that transpose through an RNA intermediate are retrotransposons. There are two types of retrotransposons: those that have direct repeats at each end, often called long terminal repeats (LTRs), and those that do not have these repeats. Pick an example of each type of retrotransposon and give (1) its basic structure and (2) its possible evolutionary history.

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One example of a retrotransposon with lo...

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Which of the following is the MOST common transposable element in humans?


A) copia
B) Alu
C) Ac
D) Ty
E) P

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

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It is estimated that transposable elements compose approximately what percent of the human genome?


A) <1%
B) 1%
C) 10%
D) 50%
E) 99%

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

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Assume that a base-pair substitution mutation converts a DNA triplet (AAT) to another DNA triplet (AAA) . A second mutation now changes the AAA triplet to the GAA triplet. (UUA and CUU code for leucine and UUU codes for phenylalanine.) This second mutation is an example of a(n) :


A) transversion.
B) intragenic suppressor.
C) loss-of-function mutation.
D) intergenic suppressor.
E) frameshift.

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

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The disorder xeroderma pigmentosum is associated with a defect in what type of DNA repair system?


A) mismatch repair
B) base-excision repair
C) photoreactivation
D) nucleotide-excision repair
E) homologous recombination

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

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Transposition can involve exchange of DNA sequences and recombination, which often leads to DNA:


A) acetylation.
B) rearrangements.
C) condensation.
D) repair.
E) replication.

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

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Which of the following is characteristic of retrotransposons?


A) They use transposase to transpose to new sites.
B) They have inverted repeats at each of their ends.
C) They transpose through an RNA intermediate.
D) They make transposase.
E) They are found only in prokaryotes.

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

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What is the difference between a mutagen and a carcinogen?

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A mutagen is a substance or agent that c...

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Fragile-X syndrome is an example of a disease caused by what type of mutation?


A) nonsense mutation
B) frameshift mutation
C) expanding nucleotide repeat
D) loss-of-function mutation
E) gain-of-function mutation

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

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Strains of E. coli that are defective in mismatch repair have very high levels of spontaneous mutagenesis. Studies have shown that in wild-type strains A:C and G:T mispairings (as opposed to the normal A:T and G:C pairings) that occur during DNA replication are more likely than other mispairings (A:G, etc.) to be detected and repaired in these mismatch repair-proficient, wild-type strains. Which of the following types of base substitutions would you expect to be most common among the spectrum of spontaneous mutations created by the mutant mismatch repair-defective strains?


A) A-to-C
B) C-to-A
C) G-to-C
D) A-to-G
E) A-to-T

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

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Helen has type I osteogenesis imperfecta (OI) , a genetic skeletal disorder. Shown below is her DNA sequence for a portion of the coding region of the collagen type I gene, which contains the mutation responsible for her disorder. The corresponding wild-type sequence is shown also (only one DNA strand is shown in each case) . Helen has type I osteogenesis imperfecta (OI) , a genetic skeletal disorder. Shown below is her DNA sequence for a portion of the coding region of the collagen type I gene, which contains the mutation responsible for her disorder. The corresponding wild-type sequence is shown also (only one DNA strand is shown in each case) .   What type of mutation does Helen carry? A)  missense B)  nonsense C)  silent D)  deletion E)  frameshift What type of mutation does Helen carry?


A) missense
B) nonsense
C) silent
D) deletion
E) frameshift

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

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The following nucleotide sequence is found in a short stretch of DNA: 5ʹ TGCC 3ʹ 3ʹ ACGG 5ʹ Suppose a depurination event occurred within the top strand. If this mutant strand were used as a template for replication, what is the MOST likely sequence of the newly synthesized strand?


A) 3ʹ AAGG 5ʹ
B) 3ʹ TACC 5ʹ
C) 3ʹ AGGG 5ʹ
D) 3ʹ TTCC 5ʹ
E) 3ʹ AGG 5ʹ

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

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A mutation that changes a GC base pair to AT is a(n) :


A) transition.
B) transversion.
C) induced mutation.
D) missense mutation.
E) synonymous mutation.

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

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What are the differences between neutral mutations and silent mutations?

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Neutral mutations and silent mutations a...

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What is the function of DNA glycosylases?


A) to recognize and cleave phosphodiester bonds in DNA
B) to recognize and remove modified bases from the sugar component of DNA
C) to reattach the two parts of DNA that result from double-strand breaks
D) to remove pyrimidine dimers from DNA of E. coli that result from exposure to UV light
E) to prevent strand slippage during DNA replication

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

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Huntington's disease can strike at an earlier age and bring about a more rapid degeneration and death in successive generations within a family. This phenomenon can be explained by which mechanism?


A) presence of a transposable element in the gene
B) chronic exposure to mutagens in the environment
C) expansion of a trinucleotide repeat in the coding sequence of the gene
D) presence of an extra chromosome in the germ line
E) absence of a gene product that is involved in DNA repair

F) A) and E)
G) C) and E)

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