Mad scientists to fall back on “CRISPR off switch” in case human gene editing goes horribly wrong
01/25/2017 // Vicki Batts // Views

The gene editing technology known as CRISPR-Cas9 has been a subject of controversy ever since it was developed. CRISPR -Cas9 gives scientists the ability to conduct genome editing with a quickness and ease never seen before. Regardless of the inherent concerns that come along with gene editing, this technology has undoubtedly changed the world of basic and applied biology indefinitely.

Perhaps one of the most concerning aspects about CRISPR-Cas9 was the inability for scientists to turn off the gene altering sequence. The potential for wrong genes to be snipped away and the consequential introduction of rogue genetic changes in human or animal DNA into the gene pool was (and still is) rather terrifying. Now, however, scientists claim that they have found a way to hopefully mitigate this tremendous risk. In a new study, researchers say that they have found a tiny protein that can actually turn off Cas9 and prevent it from creating unwanted gene alterations. They say that the protein works on human cells -- at least if they are in a petri dish. (RELATED: Read more news about modern science at Scientific.news.)

Understanding CRISPR-Cas9 Technology

CRISPR-Cas9 technology is actually comprised of two parts. CRISPR stands for "clustered regularly interspaced short palindromic repeats."  You see, DNA is made up of short blocks of repeating base pairs that are set apart by "spacer DNA." Through the action of bacteria copying and inserting the viral DNA sequence into the CRISPR region, two strands of RNA can be produced.

After that, the RNA then associates with an enzyme known as Cas9, which is described as acting like a "pair of guided scissors." Cas9 hones in on the targeted viral DNA and cuts it away. Then, the DNA is repaired by the cell and the deleted piece of DNA is replaced with a substitute portion of DNA, which is supplied by the scientists.

Brighteon.TV

The CRISPR/Cas9 technology is often explained as a "find and replace" function for genetics. Essentially, CRISPR finds the targeted piece of DNA, and Cas9 snips it out of the DNA sequence. (RELATED: Also see more news about genetically modified organisms at GMO.news)

The "off switch"

The concerns about unintended DNA alterations primarily lie at the feet of the Cas9 portion of the technology. Sometimes, it cuts the wrong portion of the DNA. It also has a tendency to remain present and active for too long, resulting in the potential for it to make more, unintended cuts to the DNA. It takes just about 24 hours for just half of the Cas9 enzyme to be degraded by cell, which means it has plenty of time to make off-target alterations.

Study author Joseph Bondy-Denomy, a microbiologist from the University of California at San Francisco, claims that an "off switch" would make the Cas9 tech quite a bit safer.

Based on the logic that in order to replicate, viruses often insert their own DNA into the bacteria's genome, commandeering the cell’s genetic equipment to copy viral DNA, it would seem that viruses must also possess a way to reverse the process and deactivate CRISPR/Cas9. Otherwise, it is possible that the bacteria might identify the viral DNA in its own genome, which would invariably lead to self-destruction.

Bondy-Denomy told Live Science, "Cas9 should make an RNA that will then cleave the virus that happens to be in its own genome — it's not smart enough to know it's in its own genome. " The research group posited that if the bacterial cell is stable and it's not self-destructing, "then perhaps this virus is making an inhibitor protein."

Although the team was able to identify four potential "anti-CRISPR" proteins, only two seem to have worked in initial petri dish testing. And while these proteins seem to deactivate the CRISPR-Cas9 process, the scientists have not yet actually proved that this new find will prevent off-target gene editing.

The research team has no idea if the proteins will actually prevent unintended DNA snipping and editing, nor do they know how long the proteins will linger in the cells or what kind of effects they may also produce.

Sources:

LiveScience.com

BerkeleyScienceReview.com



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