Not exact matches
One of these proteins, a DNA -
cutting enzyme called Cas9, binds to short RNA guide strands that
target specific
sequences, telling Cas9 where to make its
cuts.
No one disputes that UC Berkeley's Jennifer Doudna, working with Emmanuelle Charpentier, then with Umeå University in Sweden, developed the key components of the CRISPR technology — a bacterial enzyme that finds a
targeted DNA
sequence and
cuts it — and first showed in the 28 June 2012 online issue of Science that it could edit DNA in prokaryotes.
CRISPR — Cas9 uses an RNA molecule to
target DNA,
cutting to a known, user - selected
sequence in the
target genome.
But co-first authors Janice Chen, Enbo Ma and Lucas Harrington in Doudna's lab discovered that when Cas12a binds and
cuts a
targeted double - stranded DNA
sequence, it unexpectedly unleashes indiscriminate
cutting of all single - stranded DNA in a test tube.
CRISPR, originally discovered by biologists studying the bacterial immune system, consists of a DNA -
cutting enzyme called Cas9 and short RNA guide strands that
target specific
sequences of the genome, telling Cas9 where to make its
cuts.
Liu and coworkers developed last year's base editor by combining three proteins: a cytidine deaminase, a natural enzyme that converts C to uridine (U); a mutated Cas9 CRISPR enzyme that doesn't
cut DNA but uses an associated guide RNA to
target specific DNA
sequences; and a protein that prevents reversion of U back to C.
In REPAIR, the deactivated Cas13b enzyme seeks out a
target sequence of RNA, and the ADAR2 element performs the base conversion without
cutting the transcript or relying on any of the cell's native machinery.
The resulting CRISPR - Cas9 genome editing module was elegantly simple: A snippet of RNA guides the DNA - cleaving Cas9 enzyme to a matching
sequence in the genome, whereupon the enzyme
cuts the DNA, inactivating the
target sequence.
Then biologists could use it to easily
target and
cut any DNA
sequence.
First, an enzyme called Cas13 finds and
cuts an RNA
sequence of interest (the
target RNA), and when it does, it also
cuts a bunch of RNA around the
target.
On this front, Yildiz, working with CRISPR - Cas9 co-discoverer Jennifer Doudna, also at Berkeley, on August 4 described in Science Advances why CRISPR - Cas9
cuts at specific
target sequences in the genome, and where the tendency for off -
target binding comes from.