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30 Cards in this Set

  • Front
  • Back

What is the movement of a transposable element from one location to another called?

Transposition

A mutation in a gene results in a protein that disrupts a protein-protein interaction. A second mutation in a different gene results in a protein that restores this interaction is called

intergenic suppressor mutation.

How do cells alter DNA in regions of the genome where transposable elements are common to block production of transposase and inhibit transposition?

Methylation

Which of the following enzymes makes single-stranded breaks at each end of the transposable element and on either side of the target sequence during transposition?

Transposase

A mutation which changes a sense codon into a different sense codon, resulting in the incorporation of a different amino acid is called a(n)

missense mutation.

During transposition, a retrotransposon may be transcribed into RNA to produce double-stranded DNA by which process?

Reverse transcription

Transposable elements make up at least what percent of human DNA?

45%

Researchers studied inheritance of Huntington disease within a family for three generations and found that both the age of onset and time to death decreased each generation. This increase in severity of the disease from generation to generation can best be explained by

expansion of nucleotide repeats.

One of the codons that specifies the amino acid Gly (GGU, GGC, GGA, and GGG) undergoes a single-base substitution to become a nonsense mutation (UAA, UAG and UGA). This mutation is a

transversion at the first position of the GGA codon.

What is the main organism used in the Ames test?

Salmonella typhimurium

Which of the following always results from transposition?

Movement of a transposable element within the genome or between genomes

Diseases caused by expanding nucleotide repeats may become more severe in each generation, which may account for the process known as

anticipation.

Breaks in double-stranded DNA molecules are most likely to result from exposure to

Ionizing radiation.

A mutation which changes the amino acid sequence of a protein without altering its function is called a(n)

neutral mutation.

What is the best characterized mutagenic DNA lesion induced by UV light?

Pyrimidine dimer

More than half of all spontaneous mutations in Drosophila result from insertion of a(n) _______________ in or near a functional gene.


transposable element

An example of a disease resulting from a loss-of-function mutation is


cystic fibrosis.

The error-prone repair system in bacteria that allows for DNA replication across damaged regions is known as

SOS repair.

Which pair of sequences below might be contained at the ends of an insertion sequence in bacteria?

5′-GCGTATAC-3′ and 5′-GTATACGC-3′

What is the process called by which fruit flies use small RNA molecules to silence transposase genes and inhibit transposition?

RNA interference

Mutations due to small insertions and deletions can arise spontaneously during DNA replication due to

strand slippage.

What is the best characterized mutagenic DNA lesion induced by UV light?

Pyrimidine dimer

Germ-line mutations

are changes in the DNA of gametes.

Breaks in double-stranded DNA molecules are most likely to result from exposure to

Ionizing radiation

What are transposable elements that transpose through an RNA intermediate called?

Retrotransposons

A mutation that restores the wild-type phenotype through a mutation in a gene other than the one containing the original mutation

is an intergenic suppressor mutation.

A mutation which changes a sense codon into a different sense codon, resulting in the incorporation of a different amino acid is called a(n)

missense mutation.

A mutation that can affect the individual in which it occurs but not that individual's offspring is a ___________ mutation.

somatic

Which of the following is an example of a base analog?


5-bromouracil

A codon that specifies leucine undergoes a single-base substitution, producing a new codon that specifies methionine. The codons that specify leucine are UUA, UUG, CUU, CUC, CUA, and CUG. The only codon that specifies methionine is AUG. Which of the following correctly describes the mutation?

A transversion at the first nucleotide position of a leucine codon