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The main stages of genetic engineering

Natural selection and genetic modification · Genetic engineering · note 2 of 2

Spec 4.11
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The main stages of genetic engineeringSpec 4.11

In short

In genetic engineering, a restriction enzyme cuts the desired gene out of the donor DNA, leaving sticky ends. The same restriction enzyme cuts open a vector, such as a bacterial plasmid, giving matching sticky ends. The enzyme ligase joins the gene into the vector to make recombinant DNA, which carries the gene into the target organism's cells.

  1. The gene for the desired characteristic is cut out of the chromosome of the donor organism using a restriction enzyme. Each restriction enzyme cuts DNA at a specific sequence of bases.
  2. The cut leaves short, unpaired strands of DNA at each end. These are called sticky ends.
  3. The vector is cut open using the same restriction enzyme, so it has matching sticky ends. A vector is something used to carry the gene into the new cell, such as a bacterial plasmid or a virus.
  4. The gene and the vector are mixed. The sticky ends join by complementary base pairing, and the enzyme ligase joins the DNA strands together permanently. This makes recombinant DNA, for example a recombinant plasmid.
  5. The vector is used to insert the gene into the cells of the target organism (for example a bacterium, or a plant or animal at an early stage of development). The organism's cells now make the protein.
Restriction enzyme
An enzyme that cuts DNA at a specific base sequence.
Sticky ends
Short, unpaired strands of DNA left at the ends of a cut, which can join with complementary sticky ends.
Ligase
An enzyme that joins pieces of DNA together.
Vector
A carrier, such as a plasmid or virus, used to insert a gene into another organism's cells.
Exam tip:

Use the same enzyme to cut both the gene and the vector. That gives matching sticky ends. Ligase then does the joining.

Flow diagram: a restriction enzyme cuts the insulin gene out of human DNA and cuts open a plasmid, leaving matching sticky ends; the sticky ends pair up, ligase joins the DNA to make a recombinant plasmid, and the plasmid is put into a bacterium which makes human insulin. (opens full size in a new tab)
Same restriction enzyme gives matching sticky ends; ligase joins them to make a recombinant plasmid.

Quick check

  1. What is genetic engineering?

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    Modifying the genome of an organism to introduce desirable characteristics.

  2. What does a GM organism contain that a normal organism does not?

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    A gene transferred from another organism.

  3. Give one example of a desirable characteristic introduced by genetic engineering.

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    For example, bacteria making human insulin, or crop plants resistant to insects.

Written and checked against the Edexcel GCSE Combined Science (1SC0) specification · Updated October 2026

Frequently asked questions

What is genetic engineering in agriculture?

In agriculture, genetic engineering means inserting a gene from another species into crop plants to give them a desirable characteristic. For example, crop plants can be given a gene for resistance to insect pests, so they are not damaged by the pest. The modified plants are called genetically modified (GM) crops.

How is human insulin made by genetic engineering?

Higher tier The human insulin gene is cut out of human DNA with a restriction enzyme, and a bacterial plasmid is cut with the same enzyme so the sticky ends match. Ligase joins the gene into the plasmid, which is then inserted into bacteria. The bacteria make human insulin, which is used to treat diabetes.

What is the difference between genetic engineering and selective breeding?

Selective breeding uses the genes already in a species, choosing parents with desired characteristics over many generations. Genetic engineering changes the genome directly, usually by inserting a gene from a different species. This makes genetic engineering quicker, and it can give an organism a characteristic coded for by another species' gene.

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