Test 3 Flashcards

(37 cards)

1
Q

__________: A test using strains of a bacterium, Salmonella typhimurium, to determine if a substance is a mutagen.

A

Ames test

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2
Q

________________: A type of DNA repair in which a modified base is removed from a DNA strand. Following base removal, a short region of the DNA strand is removed, which is then resynthesized using the complementary strand as a template.

A

Base excision repair (BER)

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3
Q

___________: When two bases opposite each other in a double helix do not conform to the AT/GC rule. For example, if A is opposite C, that would be a base mismatch.

A

Base mismatch:

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4
Q

__________: A point mutation in which one base is substituted for another base.

A

Base substitution

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5
Q

____________: The removal of an amino group from a molecule. For example, the removal of an amino group from cytosine produces uracil.

A

Deamination

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6
Q

_______________: The removal of a purine base from DNA.

A

Depurination

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7
Q

_________________: An enzyme recognizes an incorrect alteration in DNA structure and directly converts it back to a correct structure.

A

Direct repair

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8
Q

____________: A mutation that involves the addition or deletion of nucleotides not in a multiple of three and thereby shifts thee reading frame of the codon sequence downstream from the mutation.

A

Frame shift mutations

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9
Q

__________________: Occurs when the DNA strands from a sister chromatid are used to repair a lesion in the other sister chromatid.

A

Homologous recombination repair

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10
Q

_________________: A mutation caused by environmental agents.

A

Induced mutation

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11
Q

_______________________: A DNA repair system that detects a mismatch and specifically removes the segment from the newly made daughter strand.

A

Methyl-directed mismatch repair

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12
Q

_______________________: A base substitution that leads to a change in the amino acid sequence of the encoded polypeptide.

A

Missense mutation

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13
Q

__________: A permanent change in the genetic material that can be passed from cell to cell or from parent to offspring.

A

Mutation

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14
Q

________________: The joining of the broken ends of chromosomes via nonhomologous end-joining proteins.

A

Nonhomologous end joining

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15
Q

__________________: A mutation that involves a change from a sense codon to a stop codon.

A

Nonsense mutation

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16
Q

_____________________: A DNA repair system in which several nucleotides in the damaged strand are removed from the DNA and the undamaged strand is used as a template to resynthesize a normal strand.

A

Nucleotide excision repair (NER)

17
Q

_____________________: Mutations are a random process – they can occur in any gene and do not involve exposure of an organism to a particular condition that selects for specific types of mutations.

A

Random mutation theory

18
Q

__________________: A technique in which a replica of bacterial colonies is transferred to a new petri plate.

A

Replica plating

19
Q

_________________: A mutation that does not alter the amino acid sequence of the encoded polypeptide even though the nucleotide sequence has changed.

A

Silent mutations

20
Q

____________________: A change in DNA structure that results from random abnormalities in biological processes.

A

Spontaneous mutations

21
Q

______________: A change in chemical structure such as an alternation between the keto and enol forms of the bases that are found in DNA.

A

Tautometic shift

22
Q

___________: A DNA lesion involving a covalent linkage between two adjacent thymine bases in a DNA strand.

A

Thymine dimers

23
Q

______________: A point mutation involving a change of a pyrimidine to another pyrimidine or a purine to another purine.

24
Q

____________: A point mutation in which a purine is interchanged with a pyrimidine or vice versa.

25
____________: A transcriptional regulatory protein that increases the rate of transcription.
Activator
26
___________________: Refers to the phenomenon in which a pre-mRNA can be spliced in more than one way.
Alternative splicing
27
_____________: A change in chromatin structure that alters the degree of compaction and/or the spacing (or both) of nucleosomes.
Chromatin Remodeling
28
_______________: A group of CG sequences that may be clustered near a promoter region of a gene. The methylation of the cytosine bases usually inhibits transcription.
CpG island
29
_____________: A DNA sequence that functions as a regulatory element. The binding of a regulatory transcription factor to the enhancer increases the level of transcription.
Enhancer
30
_________________: The study of mechanisms that lead to changes in gene expression that can be passed from cell to cell and are reversible, but do not involve a change in the sequence of DNA.
Epigenetics
31
_________________: An inheritance pattern in which a modification to a nuclear gene or chromosome alters gene expression in an organism, but the expression is not changed permanently over the course of many generations.
Epigenetics inheritance
32
_______________________: One of several proteins that are necessary for basal transcription at the core promoter.
General transcription factor (GTS)
33
___________________: small RNA molecules that can inhibit the expression of specific mRNAs via RNA interference.
MicroRNAs (miRNAs)
34
__________________: A protein of protein complex that binds to a regulatory element and influences the rate of transcription via RNA polymerase.
Regulatory Transcription factor:
35
_____________: A regulatory protein that binds to DNA and inhibits transcription.
Repressor
36
__________________: Small RNA molecules that silence the expression of specific mRNAs via RNA inference.
SiRNAs
37
___________________: A DNA sequence that functions as a regulatory element. The binding of a regulatory transcription factor to the silencer decreases the level of transcription.
Silencers