Notes/Biology/Paper 1/Inheritance
CAIEO Level5090§17

Inheritance

The structure of DNA and how genes control proteins; alleles, genotype and phenotype; genetic diagrams and Punnett squares for monohybrid crosses; family trees; codominance and the ABO blood groups; sex determination; continuous and discontinuous variation; mutation; and natural and artificial selection.

240 min read 15 sub-topics
106
question parts
2021–2025 · 20 papers
10 marks
per paper
≈ 8% of the paper
2.1/3
avg difficulty
moderate
#5
most examined
of 22 topics by marks

In the last chapter you saw how a baby grows from a fertilised egg. That egg got half of its genetic information from the mother and half from the father. This chapter explains how that information is stored, how it is passed on, and why children look like their parents but are never exact copies.

We start with the structure of DNA and how a gene controls the making of a protein. Then we learn the language of inheritance (alleles, genotype, phenotype) and use genetic diagrams to predict the offspring of a cross. Next come blood groups, why real results differ from the predicted ratios, how sex is decided, and family trees. Last, we look at variation, mutation, and how natural and artificial selection change a population over many generations. By the end you can complete any genetic diagram the exam gives you and explain how a population evolves.

Before you start you should be able to
  • The nucleus contains chromosomes; each chromosome is one long molecule of DNA, and a gene is a short length of that DNA (Cell Division and Reproduction)

  • Human body cells are diploid (46 chromosomes in 23 pairs); gametes are haploid (23), made by meiosis; fertilisation joins two haploid nuclei to make a diploid zygote (Cell Division and Reproduction)

  • Proteins are chains of amino acids; enzymes are proteins with an active site whose shape fits one substrate (Biological Molecules, Enzymes)

  • Bacteria reproduce by binary fission; antibiotics kill bacteria but not viruses (Cell Division and Reproduction, Disease and Immunity)

By the end of this page you can
  • Describe the structure of DNA: two strands coiled into a double helix, each a chain of nucleotides, each nucleotide with a base (A, T, C or G), and bonds between paired bases (A with T, C with G) holding the strands together

  • Define a gene as a length of DNA that codes for a protein, and explain how the base sequence controls the amino-acid sequence, the shape of the protein and so the working of the cell

  • Describe inheritance; define allele; use the terms dominant, recessive, genotype, phenotype, homozygous, heterozygous and pure-breeding

  • Use genetic diagrams and Punnett squares to predict monohybrid crosses, and give the result as a ratio (3 : 1, 1 : 1), a fraction, a percentage or a probability

  • Work backwards from offspring to the genotypes of the parents, including crossing with a homozygous recessive to find an unknown genotype

  • Explain codominance using the ABO blood groups and the alleles IAI^A, IBI^B and IOI^O

  • Explain why observed ratios often differ from expected ratios, especially with small numbers of offspring

  • Describe sex determination in humans (XX and XY) and combine the chance of a boy or girl with the chance of a phenotype

  • Read family trees (pedigrees) to decide whether an allele is dominant or recessive and to find genotypes and probabilities

  • Describe variation; tell continuous from discontinuous variation and their causes; investigate variation and draw the right graph (histogram or bar chart)

  • Describe gene mutation (sickle cell anaemia) and chromosome mutation (Down's syndrome); state the sources of genetic variation and that ionising radiation and some chemicals increase the rate of mutation

  • Describe natural selection and how it makes a population evolve, using antibiotic-resistant bacteria (MRSA) as an example

  • Describe artificial selection (selective breeding) and its role in producing economically important plants and animals

01

The structure of DNA

Syllabus requirement · §17.2.1

“

17.2.1 Describe the structure of a DNA molecule: (a) two strands coiled together to form a double helix (b) each strand is made up of a chain of nucleotides (c) each nucleotide contains a base (A, T, C, G; full names are not required) (d) bonds between pairs of bases hold the strands together (e) the bases always pair up in the same way: A with T, and C with G.

”

The one sentence to carry

DNA is two strands coiled into a double helix. Each strand is a chain of nucleotides, and each nucleotide contains one base: A, T, C or G. Bonds between pairs of bases hold the two strands together, and the bases always pair the same way: A with T, C with G.

A quick reminder

In the Cell Division and Reproduction chapter you learned that the nucleus contains chromosomes, that each chromosome is one long molecule of DNA, and that a gene is a short length of that DNA. Now we look inside the DNA molecule itself.

Five facts about the structure of DNA

Learn these five facts in the syllabus words. Exam questions ask for them almost word for word.

  1. Two strands coiled together to form a double helix. A DNA molecule has two strands (not one, not four). They twist around each other like a twisted ladder. This shape is called a double helix.
  2. Each strand is made up of a chain of nucleotides. A nucleotide is the small unit that DNA is built from. Thousands of nucleotides join end to end to make one strand.
  3. Each nucleotide contains a base. There are four kinds of base, known by their letters: A, T, C and G. You do not need their full names.
  4. Bonds between pairs of bases hold the strands together. The bases stick out from each strand into the middle. A base on one strand bonds to a base on the other strand. These bonds are the "rungs" of the ladder.
  5. The bases always pair up in the same way: A with T, and C with G. A never pairs with C or G; C never pairs with A or T. This is called base pairing.

Two more facts that Paper 2 has asked for:

  • DNA contains the elements carbon, hydrogen, oxygen, nitrogen and phosphorus (C, H, O, N and P).
  • In animal and plant cells the DNA is in the nucleus, in long straight molecules (one per chromosome). In a bacterial cell there is no nucleus: the main DNA is a circular loop lying free in the cytoplasm.
The structure of DNAdouble helixtwo strands coiled togetherunwindthe same DNA, unwoundATCGTAGCATCGone nucleotide(contains one base)each strandis a chain ofnucleotidesbonds between pairs of baseshold the strands togetherA always pairs with T; C always pairs with G

Left: a short stretch of DNA, two strands coiled into a double helix. Right: the same stretch drawn "unwound" like a ladder. Each strand is a chain of nucleotides; each nucleotide carries one base; bonds between the paired bases hold the strands together.

Using the base-pairing rule

Because A always pairs with T, and C always pairs with G, one strand tells you the other strand exactly. The two strands are called complementary.

Strand 1ATTCGA
Strand 2TAAGCT

The rule also lets you count bases in a whole DNA molecule. Every A has a T partner, so in a double-stranded molecule:

  • number of A = number of T
  • number of C = number of G

So if you know how many A bases there are, you know how many T bases there are. And the A + T pairs plus the C + G pairs make up all the base pairs.

Worked example: complementary strand and counting bases

(a) One strand of a short piece of DNA has the base sequence A T G G C A T C. Write the base sequence of the other strand.

(b) A different DNA molecule contains 200 base pairs. 70 of the bases on one strand are A and 10 are T. How many base pairs in the molecule are A–T pairs, and how many are C–G pairs?

Show full working
  1. 1

    (a) Take the first base, A. Its partner is T.

    Work one base at a time, left to right. A always pairs with T.

  2. 2

    Carry on: T → A, G → C, G → C, C → G, A → T, T → A, C → G.

    Check each pair against the rule: A–T and C–G only. A common slip is to write the same letter again instead of its partner.

  3. 3

    The other strand is T A C C G T A G.

    The second strand has the same number of bases as the first, one partner for each.

  4. 4

    (b) Every A on strand 1 is paired with a T on strand 2, and every T on strand 1 is paired with an A. So the A–T pairs = 70 + 10 = 80.

    An A–T pair can have its A on either strand, so count both the As and the Ts on the one strand you are given.

  5. 5

    All the other pairs must be C–G pairs: 200 − 80 = 120.

    There are only two kinds of pair, so the rest of the 200 pairs are C–G.

Answer

(a) T A C C G T A G. (b) 80 A–T pairs and 120 C–G pairs.

Write the pairing rule, "A–T, C–G", at the top of your working before you start.

Worked example5090/22 M/J 2025 Q6(a)3 marks

The nucleus of a cell contains DNA molecules that control cell function.

Fig. 6.1 is a diagram showing one of these DNA molecules.

Using information from Fig. 6.1:

(i) state the name of the structure labelled P

(ii) state the name of the unit of DNA labelled Q

(iii) state the letter of the base that pairs with G.

Fig. 6.1

Fig. 6.1

Show full working
  1. 1

    (i) P is the small X-shaped structure at the end of the long coiled DNA. It is a chromosome.

    The diagram shows the DNA molecule uncoiling from P. A chromosome is one long DNA molecule, tightly coiled, so P is the chromosome.

  2. 2

    (ii) Q is a box drawn around one short piece of one strand, including one base. It is a nucleotide.

    A nucleotide is the unit each strand is built from, and each nucleotide contains one base. Do not write "base" (only part of Q) or "gene" (a gene is a long length of DNA).

  3. 3

    (iii) G always pairs with C.

    The pairing rule: A with T, C with G.

Answer

(i) chromosome; (ii) nucleotide; (iii) C.

"Unit of DNA" in a question means nucleotide.

Common mistakes
  • "DNA is a single strand" or "DNA has four strands."

    DNA has two strands coiled into a double helix.

    Four is the number of different bases, not the number of strands.

  • "A pairs with G" or "C pairs with T."

    A pairs with T; C pairs with G. Always.

    Learn the pairs as two words: "AT" and "CG".

  • "The strands are held together by bonds between sugars."

    The strands are held together by bonds between pairs of bases.

    The syllabus wording is "bonds between pairs of bases hold the strands together".

  • "DNA is made of amino acids."

    DNA is made of nucleotides. It codes for the order of amino acids in a protein.

    Amino acids are the units of proteins; nucleotides are the units of DNA.

Your turn

  1. 11 mark

    One strand of DNA has the sequence G C A A T G C T. Write the sequence of the complementary strand.

    Stuck? Show hint

    Swap each base for its partner: A↔T, C↔G.

    Show solution
    1. 1

      G → C, C → G, A → T, A → T.

      Go one base at a time using the pairing rule.

    2. 2

      T → A, G → C, C → G, T → A.

      Keep the same order; do not reverse the strand.

    Answer

    C G T T A C G A

  2. 22 marks

    In a double-stranded DNA molecule, 30% of the bases are C. What percentage of the bases are G, and what percentage are A?

    Stuck? Show hint

    Every C has a G partner. What is left over must be A and T, in equal amounts.

    Show solution
    1. 1

      Every C is paired with a G, so G = C = 30%.

      Number of C = number of G in double-stranded DNA.

    2. 2

      C and G together make 30% + 30% = 60% of the bases.

      Add the two before working out what is left.

    3. 3

      A and T make the other 100% − 60% = 40%.

      All the bases are A, T, C or G, so the four must add up to 100%.

    4. 4

      A = T, so A = 40% ÷ 2 = 20%.

      A and T are always in equal numbers, so split the 40% equally.

    Answer

    G = 30%; A = 20%.

  3. 35090/22 M/J 2023 Q7(a)5 marks

    The paragraph below describes the structure of a DNA molecule.

    Complete the paragraph by writing the most appropriate word or letter in each space.

    DNA contains the chemical elements carbon, hydrogen, oxygen, ______ and ______ . Two strands of DNA coil together to form a double ______ . Each strand is made up of a chain of ______ . Bonds between pairs of bases hold the strands together. These bases always pair up in the same way: T with ______ and ______ with ______ .

    Show solution
    1. 1

      The two missing elements are nitrogen and phosphorus.

      DNA contains C, H, O, N and P. Carbohydrates contain only C, H and O, so N and P are what make DNA different.

    2. 2

      Two strands coil to form a double helix.

      "Double helix" is the name of the shape.

    3. 3

      Each strand is a chain of nucleotides.

      Nucleotides are the units of DNA.

    4. 4

      T pairs with A, and C pairs with G (or G with C).

      The pairing rule. The mark scheme gives the last mark for A + G + C all correct.

    Answer

    nitrogen; phosphorus; helix; nucleotides; A; C and G.

The rest of this note

Checking your access…

Can you do all of these?

  • Describe DNA as two strands coiled into a double helix, each a chain of nucleotides, each nucleotide with one base (A, T, C or G), with bonds between paired bases holding the strands together

  • Use the pairing rule (A–T, C–G) to write a complementary strand and to count bases

  • Define a gene, and explain how the base sequence decides the amino-acid sequence, the shape of the protein and its function, so that DNA controls the cell (e.g. through enzymes)

  • Describe inheritance, define allele, and use dominant, recessive, genotype, phenotype, homozygous, heterozygous and pure-breeding correctly

  • Draw a full genetic diagram — phenotypes, genotypes, gametes in circles, Punnett square, offspring genotypes and phenotypes, ratio — for any monohybrid cross, and give results as a ratio, fraction, percentage or probability

  • Deduce the parents' genotypes from the offspring (surprise recessive child, 3 : 1, 1 : 1) and use a cross with a homozygous recessive to find an unknown genotype

  • Explain codominance with the ABO blood groups, list the six genotypes for the four blood groups, and solve blood-group crosses and other codominance crosses (including leaving out offspring that do not survive)

  • Explain why observed ratios differ from expected ratios (random fertilisation, small numbers of offspring), and turn counts into a ratio

  • Describe sex determination (XX, XY; the sperm decides) and multiply by 1/2 for "a boy/girl with …"

  • Read a family tree: decide dominant or recessive, write certain genotypes, work outwards, and find probabilities (including 2/3)

  • Describe variation, tell continuous from discontinuous (phenotypes, causes, examples, histogram vs bar chart), and plan an investigation of both

  • Describe gene mutation (sickle cell anaemia) and chromosome mutation (Down's syndrome, 47 chromosomes); read a karyotype; state that ionising radiation and some chemicals increase the mutation rate

  • State the four sources of genetic variation: mutation, meiosis, random mating, random fertilisation

  • Describe natural selection in five parts and explain how it makes a population evolve, applying it to a new context

  • Describe how antibiotic-resistant strains such as MRSA develop, and how to reduce the risk

  • Describe the four stages of artificial selection, its uses for economically important plants and animals (and how cloning and artificial insemination help), and how it differs from natural selection