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IB Biology · Continuity and change

Mutation and gene editing practice questions.

36 exam-style questions on Mutation and gene editing — topic D1.3 of Continuity and change in the IB Biology syllabus — with answers and explanations. Samples below; the full set is free with an account.

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About this topic

Syllabus code
D1.3
Subject
IB Biology
Theme
D · Continuity and change
Questions
36 with worked answers
Question types
14 multiple-choice questions · 8 flashcards · 7 fill-in-the-gap questions · 5 true/false questions · 2 matching tasks
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Sample questions on Mutation and gene editing

Restriction enzymes are useful in genetic engineering because they:

  • Join DNA fragments together
  • Cut DNA at specific base sequences
  • Copy DNA into RNA
  • Add nucleotides to a growing strand

Answer: Cut DNA at specific base sequences

Restriction endonucleases cut DNA at specific base sequences. Staggered cuts leave single-stranded 'sticky ends' that can base-pair with complementary ends of other DNA, allowing fragments to be recombined.

In bacterial gene cloning, a plasmid is used mainly as a:

  • Source of the restriction enzymes used
  • Vector carrying a gene into a cell
  • Marker to stain DNA
  • Primer for PCR

Answer: Vector carrying a gene into a cell

Plasmids are small circular DNA molecules that replicate independently in bacteria. A gene inserted into a plasmid vector can be taken up by host cells and expressed or copied along with the plasmid.

A single base is inserted near the start of a gene's coding sequence. Determine the most likely consequence for the encoded polypeptide.

  • A single amino acid is changed
  • A frameshift altering downstream codons
  • No effect because the code is degenerate
  • Only the final codon is changed

Answer: A frameshift altering downstream codons

An insertion (not a multiple of three) shifts the reading frame, so every codon downstream is misread, usually producing a nonfunctional protein and often a premature stop.

A base substitution changes the codon GAA to GAG. Both code for glutamate. Classify this type of mutation.

  • Nonsense mutation
  • Missense mutation
  • Silent mutation
  • Frameshift mutation

Answer: Silent mutation

Because the amino acid is unchanged, the substitution is silent (synonymous), a direct consequence of the degeneracy of the genetic code at the third position.

The sickle cell allele results from a base substitution that changes one amino acid (glutamate to valine) in the beta-globin chain. Classify this mutation.

  • Silent mutation
  • Frameshift mutation
  • Missense mutation
  • Nonsense mutation

Answer: Missense mutation

A single amino acid is changed to a different one, which defines a missense mutation; the altered haemoglobin causes red blood cells to sickle under low oxygen.

State the component of the CRISPR-Cas9 system that directs the Cas9 nuclease to a specific DNA target sequence.

  • A restriction enzyme
  • A guide RNA (gRNA)
  • DNA ligase
  • A plasmid vector

Answer: A guide RNA (gRNA)

The guide RNA base-pairs with the complementary target DNA, positioning Cas9 to make a precise double-strand cut at that locus.

That was 6 of 36 Mutation and gene editing questions.

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36 Mutation and gene editing questions — free with an account. Spaced repetition, streaks and full exam simulations included.

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