AQA · GCSE · Biology

    Course version: 8461 · Version from Sept 2018

    In genetic engineering, genes from the chromosomes of humans and other…

    Full specification wording

    Genetic engineering: In genetic engineering, genes from the chromosomes of humans and other organisms can be ‘cut out’ and transferred to cells of other organisms.

    Genetic engineering is the deliberate transfer of a gene from one organism to another.

    Checked against the AQA 8461 specification (opens in a new tab) on .

    • Point 5 of 13
    • 3 key terms

    Study notes

    From the checked teaching notes for this specification point.

    The idea

    Genetic engineering is the deliberate transfer of a gene from one organism to another. A gene is a length of DNA on a chromosome that codes for a protein. Enzymes cut the gene out of the donor chromosome, leaving short single-stranded ends called sticky ends. The same enzyme cuts open a vector, often a bacterial plasmid, producing matching sticky ends. The gene is inserted so that complementary bases pair, and ligase joins the DNA. The recombinant plasmid is put into a host cell, such as a bacterium, which then reads the new gene and makes the protein.

    For example: The human insulin gene can be cut out and transferred into bacteria, which then produce insulin.

    What earns the marks

    • A gene is a section of DNA on a chromosome that codes for a particular protein.
    • Restriction enzymes cut the DNA at specific base sequences, producing fragments with sticky ends.
    • The same restriction enzyme is used to cut open a vector, such as a plasmid, so the sticky ends are complementary.
    • The donor gene and vector are joined by ligase to form recombinant DNA.
    • The vector carries the gene into a host cell, which can then express the gene and make the protein.
    • The process is described as genetic engineering because the gene is transferred artificially between organisms.

    Common mistakes and how to put them right

    • Thinking the whole chromosome is transferred.

      Put it right: Only the specific gene is cut out and moved.

    • Believing any enzyme can cut anywhere.

      Put it right: Restriction enzymes recognise specific base sequences, so the same enzyme must be used for donor DNA and vector.

    • Confusing the roles of the enzymes.

      Put it right: Restriction enzymes cut, while ligase joins DNA fragments together.

    Exam tips

    • Name the vector and the host cell in your answer, for example a plasmid placed into a bacterium.
    • Use the terms sticky ends and complementary bases to explain why the gene and vector join.
    • Link the transfer to a named product, such as human insulin made by bacteria, to show the purpose of the process.

    Try the lesson

    The start of the Genetic engineering: In genetic engineering, genes from the chromosomes of humans and other organisms can be ‘cut out’ and transferred to cells of other organisms. lesson, made from checked teaching notes for this specification point.

    Have a go first

    In genetic engineering, from which part of a human cell is a gene cut out before it is transferred to another organism?

    Listen

    Genetic engineering is the deliberate transfer of a gene from one organism to another. A gene is a length of DNA on a chromosome that codes for a protein. Enzymes cut the gene out of the donor chromosome, leaving short single-stranded ends called sticky ends. The same enzyme cuts open a vector, often a bacterial plasmid, producing matching sticky ends. The gene is inserted so that complementary bases pair, and ligase joins the DNA. The recombinant plasmid is put into a host cell, such as a bacterium, which then reads the new gene and makes the protein. For example, the human insulin gene can be cut out and transferred into bacteria, which then produce insulin. A strong answer earns marks for these points. A gene is a section of DNA on a chromosome that codes for a particular protein. Restriction enzymes cut the DNA at specific base sequences, producing fragments with sticky ends. The same restriction enzyme is used to cut open a vector, such as a plasmid, so the sticky ends are complementary. The donor gene and vector are joined by ligase to form recombinant DNA. Exam tip: Name the vector and the host cell in your answer, for example a plasmid placed into a bacterium.

    See it

    A flowchart running from top to bottom. The donor chromosome with the gene leads to the gene being cut out by a restriction enzyme, giving a gene with sticky ends. Separately, a vector such as a bacterial plasmid is cut open by the same restriction enzyme, giving a vector with matching sticky ends. Both the gene with sticky ends and the vector with matching sticky ends lead to the gene being inserted so that complementary bases pair. This leads to ligase joining the DNA to form recombinant DNA. The recombinant DNA leads to the vector carrying the gene into a host cell such as a bacterium, and finally the host cell makes the protein, for example human insulin.
    It shows the steps of genetic engineering, from cutting a gene out of a donor chromosome to a host cell making the protein.

    Key words

    Say what each word means before you turn the card.

    Gene

    Try answering aloud or in your head before turning the card.

    Sticky ends

    Try answering aloud or in your head before turning the card.

    Ligase

    Try answering aloud or in your head before turning the card.

    See every definition
    Gene
    A length of DNA on a chromosome that codes for a protein.
    Sticky ends
    Short single-stranded ends left when enzymes cut a gene out of the donor chromosome.
    Ligase
    Joins the DNA after the gene is inserted so that complementary bases pair.

    Label the diagram

    Some boxes have lost their names. Pick the right name for each number.

    The diagram again, with 3 boxes numbered instead of named. A flowchart running from top to bottom. The donor chromosome with the gene leads to the gene being cut out by a restriction enzyme, giving a gene with sticky ends. Separately, a vector such as a bacterial plasmid is cut open by the same restriction enzyme, giving a vector with matching sticky ends. Both the gene with sticky ends and the vector with matching sticky ends lead to the gene being inserted so that complementary bases pair. This leads to ligase joining the DNA to form recombinant DNA. The recombinant DNA leads to the vector carrying the gene into a host cell such as a bacterium, and finally the host cell makes the protein, for example human insulin.
    • 1Box 1

    • 2Box 2

    • 3Box 3

    0 of 3 labelled

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