The CRISPR/Cas9 is a system that is used to inactivate or correct certain
genes. The system has a downfall, however, because once it is turned on, it
stays on and keeps editing genes. This is no bueno because it can cause editing
of genes that are not supposed to be cut or corrected.
The original CRISPR/Cas9 system uses a guide RNA that matches the
desired sequence and directs the Cas9 enzyme to the location on the gene where
it will perform gene editing.
Researchers from at the University of California have developed a new method using “chemically modified RNA
base-drugs” that are still able to direct the Cas9 enzyme to the gene for editing.
What’s different is that this new RNA is able to activate and inactivate the Cas9
enzyme as needed (or wanted) by the researcher.
The modified RNA stops the Cas9 enzyme’s function when it runs out. Without
the presence of the modified RNA, the Cas9 is unable to continue editing genes.
Which is what they want! They are also trying a different method where a second
modified guide RNA is incorporated and its main role is to shut off the first modified
guide RNA. By shutting off the first guide RNA, the CRISPR/Cas9 system is also
turned off. This is beneficial for understanding and potentially finding a
solution to certain nervous system diseases that are affected
by this mechanism.
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