Session XP: 0
B6.1 · 4.6.1.1–3Paper 2🔶 Year 10 — mostly covered

DNA & the Genome

DNA structure, the genome, genes, protein synthesis. The basis of all genetics topics.

Best score
Last attempt
Best attempt progress
0
XP earned
Watch first
MyGCSEScience · AQA Biology
DNA & the Genome — watch on MyGCSEScience
FreeScienceLessons · AQA BiologyDNA and the Genome
Key facts

DNA structure

  • DNA = double helix structure. Two strands of nucleotides wound around each other.
  • Each nucleotide contains: a sugar (deoxyribose), a phosphate group, and one of four bases.
  • Complementary base pairs: A–T (adenine–thymine) and C–G (cytosine–guanine).
  • The bases pair by hydrogen bonds. The specific pairing means DNA can be replicated accurately.
  • DNA is found in the nucleus of eukaryotic cells, coiled into chromosomes.

Genes and the genome

  • Gene = a section of DNA that codes for a specific protein.
  • Genome = the entire DNA of an organism — all the genetic information.
  • The Human Genome Project mapped all ~3 billion base pairs of human DNA.
  • Importance: identify genes linked to disease, develop targeted treatments, understand inheritance.
  • Protein synthesis: DNA base sequence → (transcription) → mRNA → (translation at ribosome) → protein.
  • A change in DNA base sequence = mutation. May change the protein produced.
Exam questions — 3 questions · 9 marks
Extended questions included. Read the hint. Write in full sentences. AI marks against the AQA mark scheme.
1 markComplementary base pairingAQA 8461 style

A section of DNA has the sequence ATCGGA. What is the complementary base sequence on the other strand?

A ATCGGA
B TAGCCT
C UAGCCU
D TACGGT
4 marksProtein synthesis chainAQA 8461 P2 style

Describe the process by which DNA is used to synthesise a protein. (4 marks)

Hint: Two stages: transcription (DNA → mRNA in nucleus) → translation (mRNA → protein at ribosome). Mention codons and amino acids.
+40 XP
1 markGenome significanceAQA 8461 style

Why is knowledge of the human genome important for medicine?

A It allows scientists to create new genetic mutations deliberately
B It allows identification of genes associated with inherited diseases, enabling earlier diagnosis and development of targeted treatments
C It means all genetic diseases can now be cured by gene therapy
D It replaces the need for clinical trials

Module complete! 🎉

Score loading...

+10 XP