CCEA A-Level Life and Health Sciences 0008
Experimental Techniques
Human Body Systems
Physical Chemistry in Industrial Processes
Brain ScienceDouble Award
Material ScienceDouble Award
Medicine, Drugs and Clinical TrialsDouble Award
Scientific Method, Investigation, Analysis and Evaluation
Organic Chemistry
Medical PhysicsA2 option
Sound and LightA2 option
Genetics, Stem Cell Research and CloningA2 option
MicrobiologyDouble Award
Oral Health and DentistryDouble Award
Histology and PathologyDouble Award
Analytical Chemistry TechniquesDouble Award
Enabling TechnologyDouble Award
Genetics, Stem Cell Research and Cloning
- 13 subtopics
- 39 things to know
- A2 5
- A2 3 to A2 5, one of three (two for the Double Award)
What Genetics, Stem Cell Research and Cloning covers
Genetics, Stem Cell Research and Cloning is examined in Unit A2 5, Genetics, Stem Cell Research and Cloning — examined, one of three optional units (Single Award takes one, Double Award two). It covers DNA structure and the evidence for the double helix, RNA, genes and the triplet code, genotype, phenotype and monohybrid inheritance, dihybrid crosses, epistasis and the chi-squared test, DNA replication and the Meselson–Stahl experiment, meiosis and genetic variation, insulin, factor VIII and chymosin from genetically modified microbes, recombinant DNA technology and gene cloning, genetic engineering, food supply and ethics, gene therapy and cystic fibrosis, genetic disease, screening and counselling, genetic fingerprinting and gel electrophoresis and stem cells, therapeutic cloning and their ethics.
Where it is assessed
A2 5
Genetics, Stem Cell Research and Cloning — a written examination, one of three (two for Double Award).
Check the CCEA specification ↗The 13 subtopics
Each one has its own page.
- DNA structure and the evidence for the double helixNucleotides and the sugar–phosphate backbone, base pairing and hydrogen bonds, the stability of the double helix, Chargaff's rule with worked percentages, and the work of Franklin, Wilkins, Watson and Crick.Open →
- RNA, genes and the triplet codeRNA against DNA, messenger, transfer and ribosomal RNA, genes, loci and polypeptides, the triplet code with a worked base count, mutations and new alleles, substitutions and frameshift deletions.Open →
- Genotype, phenotype and monohybrid inheritanceGenotype and phenotype, dominant, recessive and codominant alleles, carrier crosses and probabilities, test crosses, sickle cell trait, sex linkage and haemophilia, and ABO multiple alleles.Open →
- Dihybrid crosses, epistasis and the chi-squared testDihybrid crosses and gametes, the 9:3:3:1 and test cross ratios, autosomal linkage and recombinants, epistasis in Labradors, and chi-squared tests on genetic crosses with worked values.Open →
- DNA replication and the Meselson–Stahl experimentConservative, semi-conservative and dispersive theories, the roles of helicase and DNA polymerase, and how Meselson and Stahl's 1958 nitrogen isotope experiment supported semi-conservative replication.Open →
- Meiosis and genetic variationHaploid gametes, homologous chromosomes, the two divisions of meiosis, independent segregation with worked combinations, crossing over and recombination, meiosis against mitosis and non-disjunction.Open →
- Insulin, factor VIII and chymosin from genetically modified microbesInsulin and diabetes, animal insulin and its problems, making human insulin with reverse transcriptase, Humulin and yeast, factor VIII and haemophilia, and rennet and chymosin in cheese making.Open →
- Recombinant DNA technology and gene cloningGene cloning and recombinant DNA, restriction enzymes and sticky ends, DNA ligase, vectors and plasmid uptake, marker genes, transgenic organisms, and medical and industrial uses of cloning.Open →
- Genetic engineering, food supply and ethicsSelective breeding against genetic engineering, crop yields and Golden Rice, transgenic animals producing human proteins such as albumin, and the ethical, environmental, economic and humanitarian arguments.Open →
- Gene therapy and cystic fibrosisGene therapy and its three approaches, somatic and germ cell therapy and UK law, the CFTR protein and cystic fibrosis symptoms, and early gene therapy trials with liposome and virus vectors.Open →
- Genetic disease, screening and counsellingSickle cell anaemia and malaria, aneuploidy, DNA sequencing, probes and PCR in screening, genetic counselling, oncogenes and tumour testing, carrier risk calculations and evaluating genetic testing.Open →
- Genetic fingerprinting and gel electrophoresisWhy DNA identifies individuals, Jeffreys' genetic fingerprinting, the stages of PCR, primers, gel electrophoresis and DNA ladders, paternity, forensics, breeding and marker probabilities.Open →
- Stem cells, therapeutic cloning and their ethicsTotipotent, pluripotent and adult stem cells, bone marrow transplants for leukaemia, Dolly the sheep, therapeutic and reproductive cloning, induced pluripotent stem cells, and the ethics and regulation of embryo research.Open →
What you need to know
Answer each one before you reveal it.
How does epistasis explain the 9 : 3 : 4 ratio of black, chocolate and yellow Labrador puppies?
Why is DNA described as an information-carrying molecule?
Define genotype.
Why must DNA be copied exactly before a cell divides?
What is meiosis?
What type of molecule is insulin, and where in the body is it made?
What is gene cloning?
How does traditional selective breeding improve farm animals?
What is gene therapy?
How can an allele be useful in one context but harmful in another? Use sickle cell anaemia as the example.
Why can DNA be used to tell one individual from another?
What is a stem cell?
Name the three components of a DNA nucleotide.
How does the structure of RNA differ from that of DNA?
Define phenotype.
What is a dihybrid cross?
What did the conservative theory of DNA replication propose?
Why is it important that gametes are haploid?
What is the underlying fault in diabetes mellitus that insulin treatment corrects?
What is recombinant DNA?
Evaluate genetic engineering compared with traditional breeding in animals.
State the three ways in which gene therapy can work.
What mutation causes sickle cell anaemia?
Who developed genetic fingerprinting, and when?
Why are stem cells important in the body?
How are nucleotides joined to form a single strand of DNA?
What is messenger RNA, and what does it do?
Why can identical twins differ in body mass even though their genotypes are the same?
Which gametes can an individual with genotype AaBb produce if the two genes are on different chromosomes?
What did the semi-conservative theory of DNA replication propose?
State the diploid and haploid chromosome numbers of a human.
Why is insulin given by injection rather than swallowed as a tablet?
What do restriction enzymes do?
Why can selective breeding harm the health of animals?
Explain how gene therapy supplements a defective gene.
How does haemoglobin S lead to the symptoms of sickle cell anaemia?
Describe the three temperature stages of one PCR cycle.
How do stem cells differ from all other cells in the body?
Take Genetics, Stem Cell Research and Cloning further
The same content, four other ways.
Commonly confused
Pairs that lose marks when they are blurred together.
Genotype vs Phenotype
Genotype: the set of alleles an organism carries. Phenotype: the observable features resulting from alleles and environment.
Homozygous vs Heterozygous
Homozygous: carrying two identical alleles at one locus. Heterozygous: carrying two different alleles at one locus.
Totipotent vs Pluripotent
Totipotent: able to form every cell type including the placenta. Pluripotent: able to form almost every body cell type but not the placenta.
Questions from this topic
Each one with the model answer underneath.
- 1
Why is DNA described as an information-carrying molecule?
Model answer
DNA stores information as the order of its bases along each strand. The base sequence determines the structure of the proteins a cell makes, including its enzymes.
- 2
Name the three components of a DNA nucleotide.
Model answer
A DNA nucleotide contains the sugar deoxyribose, a phosphate group and a nitrogen-containing base. The base is adenine, cytosine, guanine or thymine.
- 3
How are nucleotides joined to form a single strand of DNA?
Model answer
The phosphate of one nucleotide bonds to the deoxyribose of the next in a condensation reaction. The repeated sugar and phosphate groups form a sugar-phosphate backbone with the bases sticking out.
- 4
Which bases pair together in DNA, and how many hydrogen bonds link each pair?
Model answer
Adenine pairs with thymine through two hydrogen bonds. Cytosine pairs with guanine through three hydrogen bonds.
- 5
Describe how the two strands of a DNA molecule are arranged.
Model answer
Two sugar-phosphate backbones run in opposite directions, so the strands are antiparallel. Hydrogen bonds between paired bases hold the strands together, and the pair twists into a double helix.
- 6
Why is the width of the DNA double helix the same all along its length?
Model answer
A large two-ring base, adenine or guanine, always pairs with a small one-ring base, thymine or cytosine. Every rung of the ladder is therefore the same length.
What is inside Levo
Six ways to work the same material.
Genetics, Stem Cell Research and Cloning revision questions
- What does Genetics, Stem Cell Research and Cloning cover in CCEA A-Level Life and Health Sciences?
- 13 subtopics: dna structure and the evidence for the double helix, rna, genes and the triplet code, genotype, phenotype and monohybrid inheritance, dihybrid crosses, epistasis and the chi-squared test, dna replication and the meselson–stahl experiment, meiosis and genetic variation, insulin, factor viii and chymosin from genetically modified microbes, recombinant dna technology and gene cloning, genetic engineering, food supply and ethics, gene therapy and cystic fibrosis, genetic disease, screening and counselling, genetic fingerprinting and gel electrophoresis and stem cells, therapeutic cloning and their ethics. Each one has its own page with questions and model answers.
- How is Genetics, Stem Cell Research and Cloning organised?
- By the CCEA 0008 specification, subtopic by subtopic, so it matches the order you are taught it in.
Every question in Genetics, Stem Cell Research and Cloning, 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.
Or £46 a year, about £3.83 a month. Cancel anytime.