Game-changing technology enables faster, cheaper gene editing

Ann M. Thayer, a senior correspondent at C&EN, notes that scientists have long had the ability to remove, repair or insert genetic material in cells. But the process was time consuming and expensive. CRISPR, which stands for "clustered regularly interspaced short palinodromic repeats," streamlines gene editing dramatically. Its simplicity has enabled far more scientists to get involved in such work. In a short time, they have now used CRISPR to edit genes in insects, plants, fish, rodents and monkeys.

The potential agricultural and medical applications that could result from the tool in the future have attracted the interest of venture capitalists and pharmaceutical companies. Although in some ways it seems CRISPR work is moving full-steam ahead, a couple of recent developments could check its growth. In April, Chinese scientists reported that they had attempted to alter a gene in nonviable human embryos.

The announcement sparked bioethicists to call for a more cautious approach to gene editing. The other wrench in the system is an ongoing dispute over who should be awarded the patent for inventing CRISPR. Until these issues are resolved, some investors and researchers will opt to wait on the sidelines.