CRISPR-Cas9 is a natural defence mechanism used by bacteria to attack invading viruses
Scientists have manipulated this mechanism to develop a new gene editing tool. A ‘guide’ RNA sequence is developed that will match a specific complementarynucleotide sequence in a gene
The RNA is attached to the crispr0-cas9 enzyme and essentially guides the enzyme to the target gene allowing the gene to be cut and edited
This research could help treat genetic diseases by targeting specific sequences to reverse point mutations and improve targeted gene therapy.
It also would be a great tool for molecular biology research by improving cloning and the production of transgenic species