ROCHESTER, Minn. – Gene editing has captivated scientists and medical providers with tantalizing visions of wiping out debilitating inherited diseases. Could conditions like Huntington’s disease, for example, be cured by using a tool that acts as “molecular scissors” to remove and replace disease-causing DNA? Or, would gene editing tempt some to engineer designer babies with genes encoded for superior intelligence, beauty or athletic abilities?
Gene editing technology is rapidly advancing, putting tools at the forefront of medical research. One of the best known gene editing tools is CRISPR-Cas9, which stands for clustered regularly interspaced short palindromic repeats and CRISPR-associated protein. CRISPR-Cas9 has the potential to make gene editing faster, cheaper and more accurate, which could speed basic research studies and findings.
Although Mayo Clinic does not use gene editing as part of any treatment, it is studying the implications. Megan Allyse, Ph.D., a bioethicist who works with the Bioethics Program of the Mayo Clinic Center for Individualized Medicine and the Department of Obstetrics and Gynecology, warns that, along with improvements in understanding of the genome, gene editing also poses ethical concerns.
“It’s important to have public conversations to understand the limitations of this new technology. What are best practices (for gene editing)? What are the implications? What are the misuses of technologies like this? How can we harness it to benefit patients? How do we prevent harming populations or increasing health disparities or side effects that are not acceptable?” Allyse said.
There’s a lot we don’t understand yet.
“CRISPR-Cas9 is a tool that works very well,” Allyse said. “The problem is with us and how we use the tool. Technology can be used in many ways: It can be harmful or beneficial. We know so little about the human genome and how it works. How can you edit what you don’t know?”
One concern is that gene editing won’t work the way we want it to. Allyse points to a study that found that embryos rejected attempts to replace a sequence of genetic code that coded for disease with healthy DNA.
Instead, the embryos reverted to inherited DNA from parental genomes to replace what was removed.
Another concern is that editing one portion of a gene could lead to damage or unwanted side effects in another part of that gene.
“For example, some of the genes that have been associated with intelligence have also been associated with psychopathy,” Allyse said. “Do we want to alter genetic intelligence only to risk creating psychotic problems in a different part of the genome? Is it worth the risk?”
Researchers are studying whether gene editing could be used to remove defects in embryos to prevent genetically inherited diseases. Edits to the germline (inherited) portion of the genome would then affect all future descendants of that embryo.
However, Allyse points out that we don’t have to turn to gene editing to achieve that goal. Parents can have carrier screening to learn whether they have a disease-causing variant that could be passed to children. And in vitro DNA tests can identify embryos with known genetic conditions. Parents have the option of using in vitro fertilization to implant only healthy embryos.