AP Biology · Topic 6.7

Mutations Practice

Part of Gene Expression and Regulation.(IST-2.C)

Practice questions

10

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Sample questions

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  1. Sample 1difficulty 1/5

    WT: ATG-AAA-CCC-TAA A: ATG-AAG-CCC-TAA B: ATG-AAA-CCC-TAG (early stop) C: ATG-AAA-CCT-AAA D: ATG-AAA-ACC-CTA-A Compare to WT

    Which mutant most likely results in a frameshift?

    • A

      A

    • B

      D

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    • C

      B

    • D

      C

    Why

    Mutant D inserts an extra base (A) after AAA, shifting the downstream reading frame. Mutant A is silent/missense, B is nonsense (premature stop), C is a single-base substitution that does not change frame.

  2. Sample 2difficulty 2/5

    A nonsense mutation

    • A

      Changes a codon so it encodes a different amino acid

    • B

      Inserts a base, shifting the reading frame for all downstream codons

    • C

      Changes a codon to a synonymous one, leaving protein unchanged

    • D

      Changes a codon to a stop codon, truncating the protein

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    Why

    Truncated proteins are usually nonfunctional and rapidly degraded.

  3. Sample 3difficulty 2/5

    UV light typically causes

    • A

      Frameshift insertions (e.g., extra bases), which shift reading frames and require repair

    • B

      Double-strand breaks (e.g., chromosome fragments), which separate DNA and require repair

    • C

      Pyrimidine dimers (e.g., thymine-thymine), which distort DNA and require repair

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    • D

      Single base substitutions (e.g., G-to-A), which alter codons and require repair

    Why

    UV damage forms covalent bonds between adjacent thymines, blocking replication unless repaired by NER (nucleotide excision repair).

  4. Sample 4difficulty 2/5

    A silent mutation

    • A

      Changes a single nucleotide but, due to code redundancy, leaves the encoded amino acid unchanged

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    • B

      Changes a single nucleotide and creates a premature stop codon, truncating the protein

    • C

      Inserts a single nucleotide and shifts the reading frame for all downstream codons

    • D

      Changes a single nucleotide and substitutes one amino acid for another in the protein

    Why

    Point mutation in a degenerate position has no effect on the protein sequence.

  5. Sample 5difficulty 2/5

    A missense mutation

    • A

      Changes one nucleotide so the codon still encodes the same amino acid

    • B

      Changes one nucleotide so the codon becomes a premature stop signal

    • C

      Deletes one nucleotide, shifting the reading frame for downstream codons

    • D

      Changes one nucleotide so the codon encodes a different amino acid

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    Why

    Sickle-cell anemia is caused by a missense mutation: glutamic acid → valine at position 6 of β-globin.