For
precise genome editing, it is important to control the activity
of sequence-specific nucleases. We have constructed a chemically inducible
nuclease system based on the dimerization of FKBP and FRB domains
in the presence of rapamycin and designated it as a chemically inducible
dimerization (CID). The CID was designed to occur at the interlinker
section between DNA binding domains and the FokI catalytic domain.
Thus, induction of cleavage should occur quickly after addition of
rapamycin because components of proteins are already in active form
and located in the nucleus. This CID-dependent sequence-specific nuclease
has potential to be applied for time-resolved analysis of the mutation
induction mechanism in the genome.