AQA A-Level Biology Paper 2, June 2025: Question 8
10 marks · Medium difficulty · Extended Answer
Calculate the age of an embryo from mutation rate data, explain why prokaryote proteomes are easier to determine than eukaryote proteomes and how this aids disease prevention, and evaluate evidence linking VNTR repeats to breast cancer risk.
Practise this questionQuestion
Question text
08.1 A study of cells from a human embryo found that 2.66 × 10–7 % of the genome of one
cell had changed due to mutation.
You can assume that:
• the genome contains 3 × 109 nucleotides
• the mean rate of mutation is 1.14 mutations per cell cycle
• the cell cycle lasts 24 hours.
Use this information to calculate the age of the embryo in days.
Show your working.
[2 marks]
Answer days
The genome of the bacterium Escherichia coli is approximately 4.6 million base pairs
in length and contains around 4000 genes.
08.2 The analysis of the genome of E. coli allows the proteome to be determined more
easily than that of eukaryotes.
Explain why.
[2 marks]
08.3 Determining the proteomes of bacteria has helped provide protection for individuals
and populations against some infectious diseases.
Explain how.
[2 marks]
Scientists investigated the relationship between one type of variable number tandem
repeat (VNTR) and the risk of breast cancer occurring in women.
The scientists determined the risk of breast cancer occurring in women:
• with 2, 3 or 4 repeats of the VNTR
• without the VNTR.
They calculated the odds ratio (OR) of breast cancer occurring with 2, 3 or 4 repeats
of the VNTR.
An OR is a measure of how strongly an outcome is associated with a risk factor.
The OR formula is:
risk of breast cancer occurring with the VNTR : risk of breast cancer occurring without the VNTR
Table 5 shows the scientists’ results.
Table 5
Number of VNTR repeats Odds ratio
20.55 : 1
31.58 : 1
4 25 1.94 : 1
08.4 A student concluded that the number of repeats of the VNTR is associated with the
risk of breast cancer occurring in women.
Evaluate the student’s conclusion.
[4 marks]
Mark scheme
Show the mark scheme
Question Marking Guidance Mark Comments
Correct answer of 7 (days) = 2 marks;;
Incorrect answer but shows 7 to incorrect
magnitude e.g. 700 (ignore preceding/subsequent
zeros and position of decimal point i.e. did not
divide by 100 or incorrect use of order of
magnitude) = 1 mark
OR
Incorrect answer of 168 (incorrectly multiplied by
24) = 1 mark
OR 2
08.1 (2 x
Incorrect answer shows 9 ignoring subsequent AO2)
numbers (multiplied rather than divided by 1.14) =
1 mark
OR
Incorrect but shows 6.93 (incorrect rounding of
7.98) = 1 mark
OR
Incorrect but shows 7.98 or 8 (did not divide by
1.14) = 1 mark;
1. (E. coli / prokaryotes/bacteria) do not have 1 and 2 Accept ‘It’
introns /non-coding (DNA) refers to E. coli
OR
(E. coli / prokaryotes/bacteria) only have exons /
coding (DNA)
OR
Eukaryotes contain introns / non-coding (DNA);
2 2. Accept prokaryotes
08.2 (2 x have no/fewer
2. Eukaryotes contain (more) regulatory AO1) regulatory genes
genes;
– A-LEVEL BIOLOGY – 7402/2 –
1. (Identification/isolation of) antigens; 3. 2. Accept descriptions
of (active) immunity
2. (Antigens/proteins used to develop)
2 2. Ignore antibiotics
vaccines/antitoxins/antiserums
08.3 (2 x
OR AO1)
(Antigens/proteins used) to develop
(monoclonal) antibodies;
Ignore length of
Mark points 1 and 2 are required for maximum
investigation and use
marks.
of a statistical test
1. Two repeats decreases (risk of) breast cancer;
2. Accept ‘more than
2. Three and four repeats increases (risk of) breast two repeats’
cancer;
3. Accept only 2,3 and
4 repeats
3. No results for more than 4 repeats
OR
Ignore increase in
VNTRs repeats
No results for 1 repeat
4 max increase risk of breast
08.4 (4 x cancer
OR
AO3)
Few repeats (studied);
4. Other factors affect (risk of) breast cancer
OR
Named factor (e.g. age) affects (risk of) breast
cancer;
5. Breast cancers not all same (type);
6. Sample size not known;
How to answer it
Genomes, Proteomes and Evaluating Risk Factors
This question brings together mathematical problem-solving and molecular genetics across Topic 8 (Control of Gene Expression) and Topic 2 (Cells/Pathogens):
- Multi-step quantitative skills: Calculating cell cycles from mutation percentages and orders of magnitude.
- Genome vs. proteome sequencing: Why prokaryotic proteomes are simpler to deduce than eukaryotic proteomes (introns and regulatory DNA).
- Medical applications of genomics: Identifying surface antigens to create vaccines and monoclonal antibodies.
- Critical data evaluation (AO3): Interpreting odds ratio (OR) tables and evaluating associative claims concerning VNTRs and cancer risk.
Question 08.1
Embryo Age Calculation from Mutation Frequency (2 Marks)
📐 Step-by-Step Calculation
- Find total mutations in the genome:
Convert percentage to a decimal/fraction by dividing by 100:
Fraction mutated = (2.66 × 10⁻⁷) ÷ 100 = 2.66 × 10⁻⁹
Number of mutations = (2.66 × 10⁻⁹) × (3 × 10⁹) = 7.98 mutations - Calculate total cell cycles:
Mean rate = 1.14 mutations per cycle.
Cell cycles = 7.98 ÷ 1.14 = 7 cell cycles - Convert cell cycles to days:
Each cell cycle lasts 24 hours (= 1 day).
Age = 7 × 1 = 7 days
✅ Correct Answer
7 (days) [2 marks]
- Shows an answer of 7 to an incorrect power of ten (e.g. 700 due to forgetting to divide percentage by 100).
- Calculates 168 (incorrectly multiplied cycles by 24 instead of converting to days).
- Shows 7.98 or 8 (calculated total mutations but forgot to divide by mutation rate 1.14).
- Shows 9 (multiplied by 1.14 instead of dividing).
❌ Common Errors
- Forgetting the % sign: Multiplying 2.66 × 10⁻⁷ directly by 3 × 10⁹ gives 798 mutations instead of 7.98. Remember: "%" means per hundred!
- Unit confusion (hours vs days): Multiplying 7 cycles by 24 hours gave 168, forgetting the question explicitly asks for the answer in days.
🧠 Exam Technique
Always write every single step of your working clearly. Even if you press a wrong key on your calculator and get an incorrect final number, clear intermediate values (e.g., showing 7.98 ) secure method marks.
Question 08.2
Determining Proteomes: Bacteria vs. Eukaryotes (2 Marks)
✅ Mark Scheme Points
- Mark 1: (E. coli / prokaryotes / bacteria) do not have introns / non-coding DNA
OR (E. coli) only contain exons / coding DNA
OR Eukaryotes contain introns / non-coding DNA. - Mark 2: Eukaryotes contain (more) regulatory genes / prokaryotes have fewer regulatory genes.
💡 Key Knowledge
- Proteome: The full range of proteins that a cell is capable of producing.
- In simple prokaryotes, there is almost a 1:1 relationship between DNA base sequences and mRNA/protein sequences because there is virtually no non-coding DNA.
- In eukaryotes, vast swathes of DNA consist of non-coding introns and complex regulatory regions that determine whether and when a gene is expressed.
❌ Common Errors
- Vague claims like "prokaryotes have less DNA" or "eukaryotes have more genes". You must refer specifically to introns / non-coding DNA or regulatory genes.
- Confusing introns with exons. Remember: Exons are expressed.
🧠 Exam Technique
Comparative questions require explicit points about either group or both. State clearly: "Bacteria lack introns, whereas eukaryotic DNA contains non-coding introns and more regulatory genes."
Question 08.3
Bacterial Proteomes and Disease Protection (2 Marks)
✅ Mark Scheme Points
- Mark 1: Identification / isolation of (surface) antigens;
- Mark 2: These antigens are used to develop vaccines (or antitoxins / antiserums / monoclonal antibodies);
💡 Key Knowledge
By mapping the bacterial proteome, scientists can pinpoint which specific surface proteins act as antigens. Synthesising or purifying these antigens allows production of vaccines, which stimulate memory cells and confer herd immunity on populations.
❌ Common Trap: Stating "Antibiotics"
A very common student error is suggesting proteome analysis helps develop antibiotics. Antibiotics are chemical compounds targeting cell wall synthesis or bacterial ribosomes, not antigen-specific immune products. The mark scheme explicitly states: "Ignore antibiotics".
Question 08.4
Evaluating VNTR Repeats and Breast Cancer Risk (4 Marks)
✅ Mark Scheme Points (Max 4 Marks)
*Note: Mark points 1 and 2 are essential to achieve full marks.*
- 1. [Essential]: Two repeats decreases the risk of breast cancer (odds ratio = 0.55, which is < 1).
- 2. [Essential]: Three and four repeats increase the risk of breast cancer (odds ratio = 1.58 and 1.94, which are > 1).
- 3. [Limitation]: No data / results for more than 4 repeats OR no data for 1 repeat OR only a few repeat lengths studied (2, 3, 4).
- 4. [Limitation]: Other named factors affect breast cancer risk (e.g. age, family history/genetics, lifestyle, HRT).
- 5. [Limitation]: Breast cancers are not all the same type (different mutations/mechanisms).
- 6. [Limitation]: Sample size is not known.
🧠 Understanding Odds Ratios (OR)
The definition was given in the question: risk with VNTR : risk without VNTR
- OR < 1.0 (0.55 : 1): Risk with 2 repeats is lower than without it → decreased risk.
- OR > 1.0 (1.58 : 1 and 1.94 : 1): Risk with 3 or 4 repeats is higher than without → increased risk.
❌ Common Errors
- Generalising the trend: Writing "as repeats increase, cancer risk increases" loses marks because 2 repeats actually protects against cancer compared to having no repeats.
- Vague evaluation: Writing "they didn't do a statistical test" or "study was too short" — the mark scheme explicitly says to ignore these. Stick to sample size, missing data points, and confounding risk factors.
💡 High-Scoring Structure for "Evaluate" Questions
Always balance your argument:
- Support the claim: Quote the data accurately (distinguish between OR > 1 and OR < 1).
- Challenge/limit the claim: Identify gaps in data (missing repeat numbers: 1, 5, 6+), confounding lifestyle/genetic variables, and unknown sample size.
Topics
Biology · Practical skills · 3.2 Cells · 3.4 Genetic information, variation and relationships between organisms · 3.8 The control of gene expression (A-level only) · Data analysis
Question and mark scheme from the AQA A-Level Biology examination, Paper 2, June 2025. QuestionVault is an independent revision resource; questions remain the copyright of the awarding body.