Genetic Mutations >:( Flashcards

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1
Q

What can be 4 causes of mutations?

A
  • Mistakes in cell division
  • Exposure to radiation
  • Exposure to mutagens (chemicals)
  • Virus infections
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2
Q

What’s a frameshift and what does it do to an organism’s traits?

A

A frameshift is a shift or change in the way the DNA code is read and this can change the code being expressed in genetic expression which eventually determines traits yk. . .

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3
Q

What’s the big difference between point mutations and chromosomal mutations?

A

Point mutations are changes/shifts in the DNA molecule while…

Chromosomal mutations are the changes/shifts in either the number of chromosomes in a cell’s nucleus or in the chromosome’s structure

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4
Q

List the 3 types of point mutations and what do they do in the DNA’s replication?

A

Substitution - incorrect base is added and replaces base pair

Insertion - extra nucleotide(s) is inserted during DNA replication and results in a frameshift

Deletion - Nucleotides are skipped or missed in replication resulting in a frameshift

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5
Q

What are the 4 amino acid effects that result from point mutations and how do they affect amino acids?

A

Frameshift mutation - all amino acids after the mutated amino acid are shifted in the sequence

Misense mutation– one single amino acid is changed

Silent mutation – substitution where amino acid is not affected

Nonsense mutation – amino acid ‘Stop’s prematurely

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6
Q

What are the 2 two types of point mutations that always result in frameshift mutations (amino acid effect)

A

Insertion and deletion

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7
Q

What type of mutation is in the image below?

A

Substitution

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8
Q

What kind of amino acid effect is being displayed in the image below?

A

Silent

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9
Q

What kind of amino acid mutation (effect) has been displayed in the image below?

A

Nonsense

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10
Q

1) What kind of amino acid effect has taken place in the image below
2) What types of mutations can result in that effect?

A

Frameshift, Insertion or deletion

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11
Q

What are the 4 types of chromosome mutations (genetic arrangements) and what do they do?

A

Deletion - Parts of the chromosome structure is broken off that hold many genes containing genetic code

Duplication - Certain areas of chromosomal are copied in the structure during cellular duplication (meiosis)

Inversion - The orientation of the original parts of the chromosome is inverted (flipped around) and reinserts itself into the structure therefore the alignment of the genes (DNA) will be different

Translocation - parts of the chromosome structure break off and reinsert themselves into a different chromosome structure, therefore translocating the genetic code into a diff. chromosome

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12
Q

What’s the deal with nondisjunction in chromosomal mutations?

A

Nondisjunction is the failure to separate cells during cellular division leading to a lesser-than-expected amount of chromosomes changing the ploidy of an organism which could have effects on their traits (down syndrome or wutever)

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