Gene editing is a relatively new technology, and no other method currently available is as fast, precise, and efficient as CRISPR-Cas9. It has had unprecedented success in a number of fields, particularly in medicine—allowing scientists to edit HIV out of living organisms and engineer an end to malaria through the modification of mosquitoes.
Chinese scientists asserts that they’ve already used CRISPR on a human being, and clinical trials are in the mix in many locals (including the United States). Given the expected widespread use of CRSIPR in the world of tomorrow, researchers from the Columbia University Medical Center (CUMC) are offering a word of caution. A study published in the journal Nature Methods revealed that CRISPR-Cas9 can lead to unintended mutations in a genome.
“We feel it’s critical that the scientific community consider the potential hazards of all off-target mutations caused by CRISPR, including single nucleotide mutations and mutations in non-coding regions of the genome,” co-author Stephen Tsang, from CUMC, said in a press release.
In the study, Tsang’s team sequenced the genome of mice that they had previously used CRISPR on in an attempt to cure their blindness. They looked for all possible mutations, even those that might have changed just a single nucleotide. The researchers discovered a staggering 1,500 single-nucleotide mutations and over 100 larger deletions and insertions in the genomes of two of the recipients.