These are exciting times for genetic research, though we'll have to wait for specific clinical applications
04 de novembre 2017
How to change individual letters of your DNA?
Gene editing has made another step forward. And maybe a complementary to the former one, the CRISPR-Cas9, that was proved viable by Jennifer Doudna and I explained some months ago in this post. No it is indeed more interesting. Two different approaches, base editing and CRISPR-Cas13, have been described in Science and Nature. Adenine base editing allows to correct mutations, it doesn't cut the gene to insert a new one. It is a sharp pencil rather than scisors. With CRISP-Cas13 it is possible to edit RNA, which converts genetic information into proteins. An exciting approach, you correct a book with temporary ink that disappears, rather than making a permanent mark (like in CRISPR-Cas9).
These are exciting times for genetic research, though we'll have to wait for specific clinical applications
These are exciting times for genetic research, though we'll have to wait for specific clinical applications