How genetic modification works
Cut, paste, transfer, grow.
Genetic modification works because the genetic code is UNIVERSAL β every organism uses the same A/T/C/G alphabet. So a gene from a human can be read and used by a bacterium.
The 4 basic steps:
- IDENTIFY the gene you want (e.g. human insulin gene).
- CUT IT OUT using RESTRICTION ENZYMES β molecular scissors that cut DNA at specific sequences.
- INSERT the gene into a VECTOR. The vector is usually a PLASMID (a small ring of bacterial DNA). The same restriction enzyme is used so the ends match.
- TRANSFER the plasmid into the target organism (e.g. E. coli). The bacterium now reads the human gene and makes insulin.
- GROW the modified organism in large quantities.
The trick that makes this work is the RESTRICTION ENZYME. It always cuts at the same sequence (e.g. GAATTC), leaving 'sticky ends' that can re-join with any other DNA cut by the same enzyme. So the insulin gene and the plasmid can be glued together.
- Identify β cut β insert into plasmid β transfer β grow.
- Restriction enzyme cuts DNA at specific sequences (sticky ends).
- Plasmid (small ring of DNA) is the most common VECTOR.