CCEA A-Level Biology 1010
Biological Molecules
Enzymes
Viruses and Cell Structure
Cell Physiology and Transport
Continuity of Cells
Tissues and Organs
Exchange Surfaces and Gas Exchange
Transport in Plants
The Circulatory System in Mammals
Adaptation and Biodiversity
Human Impact on Biodiversity
Homeostasis and Excretion
Immunity
Co-Ordination and Control
Populations and Communities
Ecological Energetics and Nutrient Cycling
Respiration
Photosynthesis
DNA as the Genetic Code
Gene Technology
Genes and Patterns of Inheritance
Population Genetics and Evolution
Evolutionary Trends in Plants
Gene Technology
- 11 subtopics
- 33 things to know
- Unit A2 2
What Gene Technology covers
Gene Technology is examined in Unit A2 2, Biochemistry, Genetics and Evolutionary Trends, and drawn on again in Unit A2 3, the practical skills examination. It covers the polymerase chain reaction, DNA probes and genetic markers, microarrays, pharmacogenetics and personalised medicine, genetic fingerprinting and gel electrophoresis, the stages of gene transfer, genetically modified microorganisms, transgenic animals and plants, gene therapy, genome sequencing and the Human Genome Project, gene inactivation and knockout organisms and social, ethical and ecological issues of gene technology.
Where it is assessed
Unit A2 2
Biochemistry, Genetics and Evolutionary Trends, and again in Unit A2 3, Practical Skills in Biology.
Check the CCEA specification ↗The 11 subtopics
Each one has its own page.
- The polymerase chain reactionPurpose of the polymerase chain reaction, primer in the polymerase chain reaction and why two different primers are required.Open →
- DNA probes and genetic markersDNA probe, microsatellite repeat sequence and single nucleotide polymorphism.Open →
- Microarrays, pharmacogenetics and personalised medicineDNA microarray, two distinct uses of microarray technology and personalised medicine.Open →
- Genetic fingerprinting and gel electrophoresisGenetic fingerprinting, restriction endonuclease and how DNA fragments are separated by gel electrophoresis.Open →
- The stages of gene transferSticky ends, how reverse transcriptase is used to obtain a gene and vector in gene technology.Open →
- Genetically modified microorganismsRecall questions on inserting a human gene into a bacterium, the plasmid as a vector, restriction enzymes and ligase, the production of insulin and other proteins, and the advantages over extracting the product from an animal.Open →
- Transgenic animals and plantsTransgenic organism, using transgenic animals to produce substances of pharmaceutical value and value of engineering crops that tolerate drought or salty soil.Open →
- Gene therapyGene therapy, why an absent or faulty gene can cause disease and why liposomes are sometimes preferred to viral vectors.Open →
- Genome sequencing and the Human Genome ProjectGenome of an organism, genome sequencing and two main aims of the Human Genome Project.Open →
- Gene inactivation and knockout organismsThree ways in which a gene can be made inoperative, knockout mouse and knockin mouse.Open →
- Social, ethical and ecological issues of gene technologyHow using bacterial strains ill-adapted to human physiology improves safety and suicide gene.Open →
What you need to know
Answer each one before you reveal it.
Explain why a genetic fingerprint from a crime scene that matches a suspect is strong evidence but not proof of guilt.
Describe how DNA can be extracted from plant tissue in the laboratory.
List the main stages of transferring a gene from one organism into another.
Give one advantage of using bacteriophages rather than an antibiotic to treat a bacterial infection.
Explain why an absent or faulty gene can cause disease.
In the polymerase chain reaction, to what temperature is the mixture heated in the first step, and what does this achieve?
What is a DNA probe?
Explain why milk is a convenient place to harvest a protein from a transgenic animal.
Define the genome of an organism.
State three ways in which a gene can be made inoperative.
Give two ecological risks associated with releasing genetically modified plants.
What is a primer in the polymerase chain reaction?
Why must the sample DNA be made single-stranded before a probe is applied?
How is a patient's DNA prepared before it is applied to a microarray?
How does a restriction endonuclease help in obtaining a donor gene?
Give three reasons why bacteria are convenient organisms to modify genetically.
Give the main ethical objection to producing transgenic animals for research.
What is gene therapy?
What is genome sequencing?
What is a knockin mouse?
Explain the concern that genetically modified crops may harm insects other than the pest.
Explain why two different primers are required in the polymerase chain reaction
Give one advantage of a fluorescent label over a radioactive label.
What happens when the labelled sample is applied to the microarray chip?
Which parts of the genome are examined in genetic fingerprinting?
Explain why sticky ends are so useful in gene transfer.
Why can a human gene be expressed correctly inside a bacterium?
Name the bacterium whose plasmid is widely used as a vector for putting genes into plants.
How can adding a functional gene eliminate the symptoms of a genetic disease?
Approximately how many genes were found in the human genome?
Explain why inactivating a gene sometimes produces no visible change at all.
Describe how using bacterial strains ill-adapted to human physiology improves safety.
Take Gene Technology further
The same content, four other ways.
Questions from this topic
Each one with the model answer underneath.
- 1
What is the purpose of the polymerase chain reaction?
Model answer
The polymerase chain reaction amplifies a tiny sample of DNA, producing millions of copies of a chosen target sequence in a few hours.
- 2
Name the three steps of one cycle of the polymerase chain reaction in the order they occur.
Model answer
Each cycle consists of heating to separate the strands, cooling to allow the primers to anneal, and warming to allow the polymerase to extend the primers.
- 3
To what temperature is the reaction mixture heated in the first step, and what does this achieve?
Model answer
The mixture is heated to about 95 °C, which breaks the hydrogen bonds between the base pairs so the double helix separates into two single strands.
- 4
Why is the mixture then cooled to around 55 °C?
Model answer
Cooling allows the short primers to bind by complementary base pairing to the sequences at each end of the target region, which they could not do at the higher temperature.
- 5
What is a primer in the polymerase chain reaction?
Model answer
A primer is a short single strand of DNA with a base sequence complementary to one end of the target region, which marks where copying is to begin.
- 6
Explain why two different primers are required.
Model answer
The two strands of the target run in opposite directions, so one primer is needed to bind at each end and each is complementary to a sequence on a different strand.
What is inside Levo
Six ways to work the same material.
Gene Technology revision questions
- What does Gene Technology cover in CCEA A-Level Biology?
- 11 subtopics: the polymerase chain reaction, dna probes and genetic markers, microarrays, pharmacogenetics and personalised medicine, genetic fingerprinting and gel electrophoresis, the stages of gene transfer, genetically modified microorganisms, transgenic animals and plants, gene therapy, genome sequencing and the human genome project, gene inactivation and knockout organisms and social, ethical and ecological issues of gene technology. Each one has its own page with questions and model answers.
- How is Gene Technology organised?
- By the CCEA 1010 specification, subtopic by subtopic, so it matches the order you are taught it in.
Every question in Gene Technology, on a schedule.
Attempt a question from memory, write the correct version, then attempt it again. Levo records the jump between your first attempt and your last, and brings each question back on the day you are due to forget it.
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