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DNA structure

Inheritance, variation and evolution · Reproduction · note 5 of 8

Spec 4.6.1.5
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DNA structureSpec 4.6.1.5

In short

DNA is a polymer made from four different nucleotides. Each nucleotide is a common sugar and phosphate group with one of four bases, A, C, G or T, attached to the sugar. A sequence of three bases codes for one amino acid, and the order of bases controls the order of amino acids in a protein.

DNA is a polymer made from four different nucleotides. The DNA polymer is made up of repeating nucleotide units.

Each nucleotide consists of a common sugar and phosphate group, with one of four different bases attached to the sugar. The long strands of DNA have alternating sugar and phosphate sections, and one of the four bases is attached to each sugar.

DNA contains four bases: A, C, G and T. A sequence of three bases is the code for a particular amino acid. The order of bases controls the order in which amino acids are assembled to produce a particular protein.

DNA opened out as a ladder with two sugar-phosphate backbones as the sides and base pairs A-T and C-G as the rungs, with one nucleotide (phosphate, sugar and base) ringed. (opens full size in a new tab)
Each nucleotide is a phosphate, a sugar and one base. Bases pair up: A with T, C with G.
Exam tip:

You must be able to interpret a diagram of DNA structure, but you will not be asked to draw it from memory.

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Complementary base pairing

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In the complementary strands, C is always linked to G on the opposite strand and T is always linked to A.

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Protein synthesis

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  1. Proteins are made on ribosomes, according to a template.
  2. Carrier molecules bring specific amino acids to add to the growing protein chain in the correct order.
  3. When the protein chain is complete, it folds up to form a unique shape.
  4. This unique shape lets the protein do its job, for example as an enzyme, a hormone, or a structure in the body such as collagen.
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You are not expected to know or understand the structure of mRNA or tRNA, or the detailed structure of amino acids or proteins.

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Mutations and their effects

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A change in the structure of DNA changes the order of bases. This can change the order of amino acids, so a different protein can be made. Mutations occur continuously. Most do not alter the protein, or only alter it slightly, so its appearance or function is not changed.

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A few mutations code for an altered protein with a different shape. An enzyme may no longer fit the substrate binding site, or a structural protein may lose its strength.

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Non-coding DNA

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Not all parts of DNA code for proteins. Non-coding parts of DNA can switch genes on and off, so variations in these areas may affect how genes are expressed.

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Genetic variants may influence the phenotype in two ways: in coding DNA by altering the activity of a protein, and in non-coding DNA by altering how genes are expressed.

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Exam tip:

For 'explain how a mutation changes a protein', link the chain: base sequence changes, amino acid order changes, protein folds into a different shape, so it can no longer do its job (for example an enzyme's active site no longer fits its substrate).

Written and checked against the AQA GCSE Biology (8461) specification · Updated October 2026

Frequently asked questions

Why is meiosis important for sexual reproduction?

Meiosis is important because it halves the number of chromosomes in gametes, so that fertilisation restores the full number. Human gametes have 23 chromosomes, and when an egg and a sperm join, the new cell has 46. Meiosis also makes all the gametes genetically different, which leads to variation in the offspring.

What is a genotype and phenotype?

A genotype is the alleles present for a characteristic, such as Bb, and a phenotype is how the characteristic is expressed, such as black fur. The alleles in the genotype operate at a molecular level to develop the characteristics seen in the phenotype. A black mouse could be BB or Bb, but a brown mouse must be bb.

What is a Punnett square used for in genetics?

A Punnett square is used to show the possible combinations of alleles from the gametes of two parents. Each box is equally likely, so it predicts the probability and ratio of the offspring's genotypes and phenotypes. For example, crossing two Bb mice gives a 3 : 1 ratio of black to brown, so a 25% chance of a brown mouse.

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