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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.

What you need to know

Answer each one before you reveal it.

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Key term

Why might a base substitution leave a polypeptide unchanged, while a single-base deletion is usually harmful?

Key term

How does epistasis explain the 9 : 3 : 4 ratio of black, chocolate and yellow Labrador puppies?

Key term

Why is DNA described as an information-carrying molecule?

Key term

Define genotype.

Key term

Why must DNA be copied exactly before a cell divides?

Key term

What is meiosis?

Key term

What type of molecule is insulin, and where in the body is it made?

Key term

What is gene cloning?

Key term

How does traditional selective breeding improve farm animals?

Key term

What is gene therapy?

Key term

How can an allele be useful in one context but harmful in another? Use sickle cell anaemia as the example.

Key term

Why can DNA be used to tell one individual from another?

Key term

What is a stem cell?

Key term

Name the three components of a DNA nucleotide.

Key term

How does the structure of RNA differ from that of DNA?

Key term

Define phenotype.

Key term

What is a dihybrid cross?

Key term

What did the conservative theory of DNA replication propose?

Key term

Why is it important that gametes are haploid?

Key term

What is the underlying fault in diabetes mellitus that insulin treatment corrects?

Key term

What is recombinant DNA?

Evaluation

Evaluate genetic engineering compared with traditional breeding in animals.

Key term

State the three ways in which gene therapy can work.

Key term

What mutation causes sickle cell anaemia?

Numbers

Who developed genetic fingerprinting, and when?

Key term

Why are stem cells important in the body?

Key term

How are nucleotides joined to form a single strand of DNA?

Key term

What is messenger RNA, and what does it do?

Key term

Why can identical twins differ in body mass even though their genotypes are the same?

Key term

Which gametes can an individual with genotype AaBb produce if the two genes are on different chromosomes?

Key term

What did the semi-conservative theory of DNA replication propose?

Key term

State the diploid and haploid chromosome numbers of a human.

Key term

Why is insulin given by injection rather than swallowed as a tablet?

Key term

What do restriction enzymes do?

Key term

Why can selective breeding harm the health of animals?

Key term

Explain how gene therapy supplements a defective gene.

Key term

How does haemoglobin S lead to the symptoms of sickle cell anaemia?

Process

Describe the three temperature stages of one PCR cycle.

Key term

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. 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. 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. 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. 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. 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. 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.

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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.

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