AQA · A-Level · Biology
Course version: 7402 · Version from Sept 2016
Students should be able to: explain the biological principles that…
Full specification wording
Genetic fingerprinting (A-level only): Students should be able to: explain the biological principles that underpin genetic fingerprinting techniques interpret data showing the results of gel electrophoresis to separate DNA fragments explain why scientists might use genetic fingerprinting in the fields of forensic science, medical diagnosis, animal and plant breeding.
Genetic fingerprinting analyses Variable Number Tandem Repeats (VNTRs), non-coding DNA sequences where repeat numbers differ between individuals.
Checked against the AQA 7402 specification (opens in a new tab) on .
- Point 4 of 4
- 4 key terms
Study notes
From the checked teaching notes for this specification point.
The idea
Genetic fingerprinting analyses Variable Number Tandem Repeats (VNTRs), non-coding DNA sequences where repeat numbers differ between individuals. DNA is extracted and cut with restriction endonucleases, or specific VNTR loci are amplified by PCR. Fragment lengths vary depending on the repeat number. Gel electrophoresis separates these fragments: DNA is negatively charged due to phosphate groups, so it migrates through the gel towards the anode. The gel acts as a sieve, meaning shorter fragments travel further. Fragments are transferred to a membrane by Southern blotting and detected with labelled DNA probes, producing a banding pattern. Scientists use this to match crime scene DNA in forensics, identify pathogen strains in medical diagnosis, and prevent inbreeding in animal and plant breeding by selecting genetically diverse individuals to cross.
What earns the marks
- Explain separation: DNA is negatively charged due to phosphate groups and moves towards the anode.
- Explain separation: the gel acts as a sieve, so shorter DNA fragments travel faster and further.
- Explain principles: DNA is cut with restriction endonucleases, or specific VNTR loci are amplified by PCR, producing fragments whose length depends on the number of repeats.
- Explain detection: fragments are transferred to a membrane by Southern blotting and detected using labelled DNA probes.
- Explain uses: in breeding, comparing VNTR patterns identifies genetically diverse individuals to cross, preventing inbreeding.
- Interpret gels: estimate the length of an unknown DNA fragment by comparing its position against a DNA ladder of known standard lengths.
Common mistakes and how to put them right
Stating that PCR alone replaces restriction endonucleases in all genetic fingerprinting.
Put it right: Classical genetic fingerprinting uses restriction endonucleases to cut DNA, while PCR amplification of specific VNTR loci is a modern alternative, so describe the method the question asks about.
Concluding a definitive match from a single shared band, rather than recognising that a match across multiple VNTR loci is required for a high probability of identification.
Put it right: State that several loci must match before a match is treated as strong evidence.
Stating that genetic fingerprinting sequences the whole genome, rather than remembering that it only analyses the length of specific non-coding VNTR fragments.
Put it right: Describe it as comparing fragment lengths at specific VNTR loci, not whole-genome sequencing.
Exam tips
- When interpreting a gel, explicitly quote the figure's labels (e.g., 'the band at 3 kb in lane 2') rather than making vague comparisons.
- For 'explain why' questions on fingerprinting uses, always provide both the specific field application (e.g., forensics) and the biological reason (e.g., matching VNTR profiles to place a suspect at the scene).
Try the lesson
The start of the Genetic fingerprinting (A-level only): Students should be able to: explain the biological principles that underpin genetic fingerprinting techniques interpret data showing the results of gel electrophoresis to separate DNA fragments explain why scientists might use genetic fingerprinting in the fields of forensic science, medical diagnosis, animal and plant breeding. lesson, made from checked teaching notes for this specification point.
Have a go first
Which biological principle explains why genetic fingerprinting can distinguish one person from another?
Listen
Genetic fingerprinting analyses Variable Number Tandem Repeats (VNTRs), non-coding DNA sequences where repeat numbers differ between individuals. DNA is extracted and cut with restriction endonucleases, or specific VNTR loci are amplified by PCR. Fragment lengths vary depending on the repeat number. Gel electrophoresis separates these fragments: DNA is negatively charged due to phosphate groups, so it migrates through the gel towards the anode. The gel acts as a sieve, meaning shorter fragments travel further. Fragments are transferred to a membrane by Southern blotting and detected with labelled DNA probes, producing a banding pattern. Scientists use this to match crime scene DNA in forensics, identify pathogen strains in medical diagnosis, and prevent inbreeding in animal and plant breeding by selecting genetically diverse individuals to cross. A strong answer earns marks for these points. Explain separation: DNA is negatively charged due to phosphate groups and moves towards the anode. Explain separation: the gel acts as a sieve, so shorter DNA fragments travel faster and further. Explain principles: DNA is cut with restriction endonucleases, or specific VNTR loci are amplified by PCR, producing fragments whose length depends on the number of repeats. Explain detection: fragments are transferred to a membrane by Southern blotting and detected using labelled DNA probes. A common slip: Stating that PCR alone replaces restriction endonucleases in all genetic fingerprinting. Instead, classical genetic fingerprinting uses restriction endonucleases to cut DNA, while PCR amplification of specific VNTR loci is a modern alternative, so describe the method the question asks about. Exam tip: When interpreting a gel, explicitly quote the figure's labels (e.g., 'the band at 3 kb in lane 2') rather than making vague comparisons.
Key words
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gel electrophoresis
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VNTR amplification
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restriction endonucleases and Southern blotting
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preventing inbreeding
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See every definition
- gel electrophoresis
- A process that separates DNA fragments, which are negatively charged due to phosphate groups and so migrate through the gel towards the anode, with the gel acting as a sieve so shorter fragments travel further.
- VNTR amplification
- A modern alternative in which specific VNTR loci are amplified by PCR, producing fragments whose length depends on the number of repeats.
- restriction endonucleases and Southern blotting
- DNA is cut with restriction endonucleases, then fragments are transferred to a membrane by Southern blotting and detected with labelled DNA probes, producing a banding pattern.
- preventing inbreeding
- In animal and plant breeding, comparing VNTR patterns identifies genetically diverse individuals to cross.
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