8.1: Alternation Of Sequence Of Bases In DNA Can Alter Structure Of Proteins Flashcards

1
Q

What is a mutation?

A

An alteration to the DNA base sequence. Often arise spontaneously during DNA replication.

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2
Q

What are addition and deletion mutations?

A

Where one or more nucleotides (bases) are either inserted or deleted from the DNA sequence

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3
Q

What is a substitution mutation?

A

Where one nucleotide (base) in DNA sequence is replaced by another

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4
Q

What is a duplication mutation?

A

Where one or more nucleotide (bases) duplicate and repeat

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5
Q

What is an inversion mutation?

A

Where a group of nucleotides (bases) become separated from the DNA sequence, then rejoin in the reverse order i.e. they have flipped

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6
Q

What is a translocation mutation?

A

Where a group of nucleotides (bases) become separated from the DNA sequence, and are then inserted into the DNA of a different chromosome

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7
Q

Which mutations are most likely to have a significant impact and why?

A

Insertion, deletion, duplication, translocation.
Because they produce a frameshift, meaning the entire amino acid sequence produced will be different

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8
Q

Which mutations are less likely to have an impact and why?

A

Substitution, inversion.
Because they only alter one or very few triplets, the amino acid sequence might not be affected due to the degenerate nature of the genetic code

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9
Q

Is a mutation resulting in a change to the amino acid sequence always harmful?

A

No; may be neutral if resulting change in protein has no effect on the organism.
Also may be beneficial, which is the basis for evolution and natural selection.

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10
Q

What is a mutagenic agent? Give examples of this.

A

Factors that increase rate of gene mutation. Chemical mutagens such as alcohol and benzene. Ionising radiation such as UV and x-ray

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