Chapter 13: Altering the Genetic Material: Mutation, DNA Repair, and Cancer Flashcards

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1
Q

Define mutation.

13.1

A

a heritable change in the genetic material

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2
Q

T or F: New mutations are much more likely to be harmful than beneficial to the individual.

13.1

A

true

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2
Q

What are the two basic types of change that gene mutations can cause?

13.1

A

1) the base sequence within a gene can be changed
2) one or more base pairs can be added to or removed from a gene

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3
Q

What type of mutation is this?

A wild-type DNA sequence is 5’ -ACACGTTGAT- 3’.
It is converted to 5’ -ACACGTTAAT - 3’.

13.1

A

point mutation/base substitution; where G is replaced with A

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4
Q

Where must a mutation occur if its is to directly affect an amino acid sequence?

13.1

A

the coding region of a protein-encoding gene

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5
Q

There are 4 different types of effects that point mutations have on polypeptides. Name each one and briefly describe them.

BONUS: DRAW IT!

13.1

A
  1. Silent (causes no change)
  2. Missense (changes one amino acid in the polypeptide)
  3. Nonsense (changes a normal codon to a stop codon and shortens the polypeptide)
  4. Frameshift (produces a different amino acid sequence)
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6
Q

A point mutation affects only a single ____ pair within the DNA.

13.1

A

base

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7
Q

____ and ________ mutations can cause more dramatic changes to a polypeptide sequence than ________ mutations.

13.1

A

nonsense and frameshift; missense

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8
Q

T or F: Mutations within noncoding sequences can affect gene expression.

13.1

A

true

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9
Q

What effects do the following sequences have on mutation?
Promoter, transcriptionl regulatory element, splice sites, translational regulatory element, and intergenic region.

13.1

A

Promoter: increase or decrease the rate of transcription
Transcriptional RE: alter the regulation of transcription
Splice sites: alter ability of pre-mRNA to be properly spliced
Translational RE: alter the ability of mRNA to be translationally regulated
Intergenic region: not as likely to affect gene expression

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10
Q

Define a germ-line mutation.

13.1

A

a mutation that occurs in a germ-line cell, which gives rise to gametes; can be passed from parent to offspring

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11
Q

Consider a germ-line mutation that occurs in a sperm which fertilizes a normal egg to produce a zygote. In the individual that results from this zygote ____% of the cells will contain the mutation, and ____ % of the gametes produced by that individual will carry the mutation.

13.1

A

100; 50

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12
Q

T or F: A somatic mutation is transmitted to the offspring of the individual that carries it.

13.1

A

false; it is NOT

germ-line mutations ARE passed from parent to offspring

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13
Q

T or F: Germ-line mutations affect the whole organism, while somatic mutations affect a limited area of the body.

13.1

A

true

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14
Q

Bacterial colonies can be transferred from a master plate to secondary plates in the same configuration using a transferring agent such as a sterile velevet cloth. What is this technique know as?

13.2

A

replica plating

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15
Q

Which two scientists are responsible for using replica plating to show that mutations are random events?

13.2

A

Joshua and Esther Lederberg

16
Q

The results of the replica plating experiment performed by the Lederbergs supported their hypothesis that mutations are random events by demonstrating what?

13.2

A

The T1 mutation developed in the original population before exposure to bateriophages.

17
Q

What type of mutation results from abnormalities that naturally occur during biological processes?

13.2

A

spontaneous mutations

18
Q

Define induced mutations.

13.2

A

Mutations that are caused by environmental agents that enter the cell and alter the structure of DNA.

19
Q

The technique of replica plating allows for the:

13.2

A

identification of transformed cells

20
Q

How do the effects of germ-line mutations in a parent progress over the lifetime of an offspring receiving that mutation?

13.2

A

All of the cells of the individual’s body, but only half of the gametes produced by that individual will carry the mutation.

21
Q

What are two types of physical mutagens?

13.2

A

X-rays and UV light

22
Q

What are the three outcomes that are caused by chemical mutagens?

13.2

A

1) covalent modification (ex: nitrous acid deaminates bases)
2) base analogues (ex: 5-Bromouracil and 2-Aminopurine)
3) distortion of the DNA double helix (ex: benzo[a]pyrene

23
Q

Define ioning and nonionizing radiation.

13.2

A

Ioning: Radiation that is short-wavelength and high energy, and often leads to base deletions and breaks in one or both DNA strands
Nonionizing: Radiation that has a longer wavelength and lower energy, which penetrates the skin and often leads to thymine dimers

24
Q

What are thymine dimers?

13.2

A

In DNA, a type of pyrimidine dimer that can cause a mutation; a site where two adjacent thymine bases become covalently crosslinked to each other

25
Q

Which test was developed in the 1970s, to evaluate the ability of a substance to cause muations?

13.2

A

the Ames test

26
Q

Who was the Ames test developed by?

13.2

A

Bruce Ames

27
Q

T or F: UV lights are ionizing, whereas X-ray and gamma rays are forms of nonionizing radiation.

13.2

A

false; the opposite

28
Q

T or F: All living things possess mechanisms allowing them to minimize mutation.

13.3

A

true

29
Q

Exposure to chemical mutagens can lead to mutations because chemical mutagens can cause:

Hint: 2 answers

13.2

A

insertions and deletions during DNA replication
and
inappropriate base pairing during DNA replication

30
Q

What is NER? Does it occur in prokaryotes? What about eukaryotes?

A

NER stands for nucleotide excision repair, and it is the most common DNA repair system found in all eukaryotes and prokaryotes

31
Q

A compound is subjected to the Ames test to evaluate its ability to cause mutation. If the subsance is a mutagen, what results are expected?

13.2

A

there will be more bacterial colonies on the plate exposed to the mutagen than on the control plate

32
Q

Identify the function of each protein that is involved in nucelotide excision repair in E.Coli. (UvrC, UvrD, DNA polymerase, DNA ligase, UvrA/UvrB complex)

BONUS: DRAW IT! :)

13.3

A

UvrC: cuts DNA on both sides of the damaged site
UvrD: removes the damaged region
DNA polymerase: synthesizes new DNA to fill in the gap
DNA ligase: seals newly synthesized DNA to the original strand
UvrA/UvrB complex: identifies a damaged site

33
Q

Compare base analogs to DNA bases.

13.2

A

base analog structure is similar to DNA bases but don’t pair correctly and cause errors in DNA replication
(ex: 5-Bromouracil and 2-Aminopurine)

34
Q

What is the purpose of the Ames test?

13.2

A

it’s an experimental procedure that tests whether substances cause a mutation (make histidine); uses salmonella typhimurium that cannot synthesize histidine

35
Q

Can mutagens cause mutations by altering the genetic code of an organism?

13.2

A

No; mutagens can cause mutations by chemically alterting the DNA molecule and distrupting the replication of DNA.