posted on 2016-08-09, 00:00authored byWeipeng Liu, Huiheng Yu, Xiaoming Zhou, Da Xing
The CRISPR/Cas9 system
is a revolutionary genome-editing tool that
enables targeted and efficient gene knockouts. However, the off-target
effects and loci-dependent enzyme activity limit its uses on the field
of research and treatment. In this study, we designed a convenient
and sensitive in vitro test method, which was based
on electrochemiluminescence (ECL) technology for evaluating cleavage
activity of the CRISPR/Cas9 system. It was find that Cas9 can tolerate
some common genetic modifications to its target DNA. It was also find
that target DNA/sgRNA with single-base mismatch and UV damages of
target DNA resulted in significantly reduction of Cas9 cleavage efficiency.
Comparing with traditional method, the proposed method reduced the
evaluation time from weeks to 2 h. Therefore, our study provides a
versatile in vitro method for a priori analysis of
CRISPR/Cas9 system and highlights the potential to guide in
vivo genome editing.