Topic 8-1 Flashcards

1
Q

two thymine bases covalently bind and block DNA replication

A

pyrimidine dimer

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2
Q

system allows bacterial cells to bypass the replication block with a mutation prone pathway

A

SOS system in bacteria

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3
Q

in eukaryotes, the pyrimidine dimer is replaced by AA

A

DNA polymerase eta

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4
Q

what are the main types of DNA repair mechanisms for pyrimidine dimers?

A
  • SOS system in bacteria
  • DNA pol. eta in eukaryotes
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5
Q

high energy radiation (x-rays, gamma rays) remove electrons from atoms, altering the chemical structure of bases and inducing:

A

double stranded DNA breaks

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6
Q

UV radiation causes the formation of:

A

pyrimidine dimers (usually TT, but can be TC/CC)

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7
Q

list the six main types of chemically induced mutations:

A
  • base analogs
  • alkylating agents
  • deamination
  • hydroxylamine
  • oxidative reactions
  • intercalating agents
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8
Q

resembles thymine, except that it has a bromine atom in place of a methyl group on the 5C atom

A

5-bromouracil

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9
Q

a chemically induced mutation where the chemical strucutre of a molecule resembles a nucleotide base

A

base analogs

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10
Q

a chemically induced mutation where molecules add an alkyl group to normal nucleotides

A

alkylating agents

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11
Q

________ converts guanine into 8-oxy-7,8-dihydrodeoxyguanine

A

oxidative radicals

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12
Q

molecules such as proflavin, acridine orange, etc, insert themselves between adjacent bases in DNA, distorting the 3D structure of the helix - can also cause insertions and deletions which results in frameshift mutations

A

intercalating agents

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13
Q

how do we test chemicals to identify mutagens?

A

the Ames test is used to identify chemical mutagens

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14
Q

uses his- strains of bacteria to test chemicals for their ability to produce his-/his+ mutations

A

the Ames test

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15
Q

what are forward genetic screens?

A

identify genes that contribute to a phenotype/trait. after conducting a genetic screen, we have a collection of new mutations

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16
Q

what are the two main problems with forward genetic screens?

A

1) we don’t know if some of the same genes have been hit multiple times
2) in a genetic screen, one mutant strain may have more than one mutated gene

17
Q

are crucial for the identification of new mutants

A

complementation tests

18
Q

what is the purpose of a complementation test?

A

to determine whether two mutations are alleles of the same gene

19
Q

‘parasitic’ DNA sequences that can move about the genome

A

transposable elements

20
Q

movement of the transposons. may take place through a DNA or RNA intermediate.

A

transposition

21
Q

what are the features of transposition?

A
  • flanking direct repeats
  • terminal inverted repeats
22
Q

a type of transposition where a new copy of the transposable elecment inserts in a new location, and the old copy stays behind (copy and paste)

A

replicative transpostition

23
Q

a type of transposition where the old copy excises from the old site and moves to a new site (cut and paste)

A

nonreplicative transposition

24
Q

a type of transposition which requires reverse transcription to integrate into the target site (PDF –> copy to word doc –> print to PDF)

A

RNA intermediate transposition

25
Q

in humans, about _____% of the human genome comprises sequences that are related to transposable elements, mostly _______

A

45%, retrotransposons

26
Q

transposons cause mutations by:

A
  • inserting into another gene
  • promoting chromosomal rearrangements
  • deleting and inserting genes as they move
27
Q

IS1

A

simple transposable elements found in bacteria

28
Q

Tn10

A

a composite transposon in bacteria

29
Q

who was the first person to discover transposable elements?

A

Barbara McClintock

30
Q

Ac and Ds

A

transposable elements in maize.