The main stages of genetic engineering

The main stages of genetic engineeringSpec 4.11

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.

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