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IB Biology · Theme D: Continuity and change · SL and HL

D1.1 DNA replication

A one-page summary of D1.1 DNA replication, the key terms to know, and sample exam questions with answers. For the full lesson, open the illustrated revision slides or practise in the app.

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Guiding questions

How is new DNA produced?

How has knowledge of DNA replication enabled applications in biotechnology?

What D1.1 covers

Copying the genome accurately

PCR and gel electrophoresis — DNA in the lab

HL — the replication fork in detail

D1.1 DNA replication: summary

Why replicate

  • DNA replication produces two exact copies — needed for growth, tissue replacement and reproduction.
  • It copies rather than mixes alleles; rare errors that are not corrected become mutations (D1.3).

Semi-conservative model

  • Each new molecule = one original strand + one new strand; complementary base pairing gives high accuracy.
  • Meselson–Stahl's density-gradient experiment provided the classic evidence for this model.

Helicase & DNA polymerase

  • Helicase unwinds the double helix, breaking hydrogen bonds between strands.
  • DNA polymerase builds a new strand from a template (SL: general function only).

PCR & gel electrophoresis

  • PCR amplifies DNA using primers, Taq polymerase and repeated heating/cooling cycles.
  • Gel electrophoresis separates fragments by size using an electric current; more markers tested = lower chance of a false match.

HL · Leading & lagging strands

  • DNA polymerase only builds 5'→3': the leading strand is continuous, the lagging strand is discontinuous (Okazaki fragments).
  • Primase starts each fragment; polymerase III extends it; polymerase I replaces primers; ligase seals the gaps.

HL · Proofreading

  • DNA polymerase III proofreads and replaces mismatched nucleotides as it goes, boosting accuracy further.
  • Errors that escape proofreading can become permanent mutations (D1.3).

Key terms

Semi-conservative replication
A model of DNA replication in which each new molecule keeps one original strand and one newly synthesized strand.
Primer
A short nucleotide sequence that provides the free 3' end DNA polymerase needs before it can begin extending a strand.
Taq polymerase
A heat-stable DNA polymerase, originally from a hot-spring bacterium, used to extend new strands during PCR.
DNA profiling
Comparing PCR-amplified, individually variable DNA regions to identify or match a person, e.g. in forensics or paternity testing.
Okazaki fragment HL
One of the short DNA sections making up the discontinuously synthesized lagging strand.
DNA proofreading HL
DNA polymerase III's removal and correction of a mismatched nucleotide immediately after it is added.

Sample exam questions

Three of the 39 multiple-choice questions for D1.1. Try each one before opening the answer.

Question 1. Which statement best explains why DNA replication is essential in multicellular organisms?

  1. It produces genetic variation among the organism's cells
  2. It allows growth (increase in cell number) and the replacement of damaged or worn-out tissue
  3. It supplies the energy multicellular organisms need for movement
  4. It converts RNA back into DNA in every cell
Show the answer

Answer: B. Every new cell produced by mitosis needs a complete, identical copy of the genome. DNA replication supplies that copy before each division, which is what makes growth and tissue replacement possible in a multicellular body.

Question 2. A cell enters mitosis without having fully replicated its DNA. What is the most likely direct consequence?

  1. The daughter cells will each receive a complete, extra copy of the genome
  2. The cell will produce more ATP than normal
  3. The daughter cells will not each receive a complete copy of the genetic material
  4. The rate of transcription will increase to compensate
Show the answer

Answer: C. Mitosis distributes one full set of chromosomes to each daughter cell on the assumption that replication is already complete. If replication is incomplete, at least one daughter cell will end up with missing genetic information, which is generally lethal or severely damaging to the cell.

Question 3. A mutation eliminates the 3′→5′ exonuclease (proofreading) activity of DNA polymerase III, while leaving its ability to add nucleotides unaffected. What is the most likely consequence?

  1. DNA replication would stop completely, since synthesis could no longer occur
  2. Okazaki fragments would no longer be joined together
  3. RNA primers would no longer be removed from the lagging strand
  4. The rate of nucleotide misincorporation (errors) during replication would increase significantly
Show the answer

Answer: D. Without the ability to detect and excise mismatched nucleotides, errors that would normally be caught and corrected during synthesis are instead left in place, so the overall error (mutation) rate of replication rises. Synthesis itself can still proceed, since the polymerase activity that adds nucleotides is unaffected.

Linking questions

Questions that connect D1.1 to other parts of the course, the kind that come up in Paper 2.

Practise D1.1

39 quiz questions7 data questions7 exam questionsmarkschemes included

Study notes, every question and full markschemes for D1.1 are in the app with Pro. Two lessons are completely free to try: A1.1 Water and B1.1 Carbohydrates and lipids.

Practise D1.1 in the app Revision slides