Test 3 Flashcards
(37 cards)
__________: A test using strains of a bacterium, Salmonella typhimurium, to determine if a substance is a mutagen.
Ames test
________________: 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.
Base excision repair (BER)
___________: 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.
Base mismatch:
__________: A point mutation in which one base is substituted for another base.
Base substitution
____________: The removal of an amino group from a molecule. For example, the removal of an amino group from cytosine produces uracil.
Deamination
_______________: The removal of a purine base from DNA.
Depurination
_________________: An enzyme recognizes an incorrect alteration in DNA structure and directly converts it back to a correct structure.
Direct repair
____________: 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.
Frame shift mutations
__________________: Occurs when the DNA strands from a sister chromatid are used to repair a lesion in the other sister chromatid.
Homologous recombination repair
_________________: A mutation caused by environmental agents.
Induced mutation
_______________________: A DNA repair system that detects a mismatch and specifically removes the segment from the newly made daughter strand.
Methyl-directed mismatch repair
_______________________: A base substitution that leads to a change in the amino acid sequence of the encoded polypeptide.
Missense mutation
__________: A permanent change in the genetic material that can be passed from cell to cell or from parent to offspring.
Mutation
________________: The joining of the broken ends of chromosomes via nonhomologous end-joining proteins.
Nonhomologous end joining
__________________: A mutation that involves a change from a sense codon to a stop codon.
Nonsense mutation
_____________________: 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.
Nucleotide excision repair (NER)
_____________________: 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.
Random mutation theory
__________________: A technique in which a replica of bacterial colonies is transferred to a new petri plate.
Replica plating
_________________: A mutation that does not alter the amino acid sequence of the encoded polypeptide even though the nucleotide sequence has changed.
Silent mutations
____________________: A change in DNA structure that results from random abnormalities in biological processes.
Spontaneous mutations
______________: A change in chemical structure such as an alternation between the keto and enol forms of the bases that are found in DNA.
Tautometic shift
___________: A DNA lesion involving a covalent linkage between two adjacent thymine bases in a DNA strand.
Thymine dimers
______________: A point mutation involving a change of a pyrimidine to another pyrimidine or a purine to another purine.
Transition
____________: A point mutation in which a purine is interchanged with a pyrimidine or vice versa.
Transversion