Scientists discover new approach to gene therapy
Researchers have found a promising new method for gene therapy. They successfully restarted inactive genes by bringing them closer to genetic switches on the DNA called enhancers. The intermediate piece of DNA was cut out using CRISPR-Cas9 technology. This strategy opens up new possibilities for treating genetic diseases. The team specifically shows the technology’s potential for the treatment of sickle cell disease and beta-thalassemia, two genetic blood diseases. In these conditions, a faulty gene could potentially be compensated by reactivating a helpful but normally inactive one. This ‘delete-to-recruit’ ...