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AP® Biology · Unit 6 · Topic 6.2

DNA Replication: Revision Notes (Biology 6.2)

One-page recap of DNA replication: the semiconservative model and its evidence, 5′ to 3′ synthesis, primers, the enzymes at the fork, and leading and lagging strands.

Short on time? This page is the recap. For explanations, figures and worked examples, use the full study guide.

Recap

  • Replication ensures each daughter cell receives the same hereditary information.
  • It is semiconservative: the parent strands separate, each acts as a template, and each new molecule keeps one parent strand.
  • Evidence (Meselson and Stahl, 1958): after one round in a new isotope, all DNA was intermediate (not conservative); after two rounds, two bands appeared (not dispersive).
  • DNA polymerase adds nucleotides only to a 3′ end, so DNA is made 5′ → 3′. It cannot start a chain, so it needs an RNA primer.
  • Replication starts at an origin, which opens two forks moving apart. Bacteria typically have one origin; each eukaryotic chromosome has many.

Key relationships

Enzyme or part Where Job
Topoisomerase ahead of the fork relieves supercoiling (overwinding)
Helicase at the fork separates strands by breaking hydrogen bonds between bases
RNA primer start of each new strand or fragment provides a 3′ end to build on
DNA polymerase behind the fork adds complementary nucleotides to the 3′ end; also replaces primers with DNA
Ligase lagging strand seals the backbone between fragments
Strand Direction relative to the fork Synthesis Primers
Leading towards the fork continuous one per fork
Lagging away from the fork discontinuous, in fragments one per fragment
Model After round 1 After round 2
Conservative old and new bands, 50 : 50 old 25%, new 75%
Semiconservative all hybrid hybrid 50%, all-new 50%
Dispersive one hybrid band one band, shifted further

Assumptions behind the numbers

  • Band predictions assume every molecule replicates exactly once per round.
  • Replication-time calculations assume constant fork speed, two forks per origin and all origins starting together.

Mistakes to avoid

  1. Saying the lagging strand is made 3′ → 5′.
  2. Saying helicase breaks covalent bonds, or that topoisomerase acts behind the fork.
  3. Forgetting that DNA polymerase needs a primer.
  4. Saying ligase forms hydrogen bonds.
  5. Writing a new strand without reversing it to read 5′ → 3′.
  6. Confusing “fraction of molecules containing an old strand” with “fraction of strands that are old”.

Quick self-check

  1. A template strand reads 5′-ATTGCC-3′. Write the new strand 5′ → 3′. (5′-GGCAAT-3′)
  2. DNA with both strands labelled replicates three times in unlabelled medium. What percentage of molecules contain a labelled strand? (8 molecules, 2 contain one labelled strand: 25%)
  3. A drug blocks ligase. Which strand is affected, and how? (The lagging strand stays as separate fragments; the leading strand is largely unaffected.)

Next: practice questions.

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