CRISPR works like molecular scissors that can cut DNA at specific locations. It uses two key components: the Cas9 enzyme, which cuts the DNA, and a guide RNA (gRNA) that directs Cas9 to the exact gene sequence to be edited. Once the DNA is cut, the cell naturally repairs the break. Scientists can use this process to disable a faulty gene or insert a corrected version.
This precision and simplicity make CRISPR far more efficient than older gene-editing methods, which were slow, expensive, and less accurate.