Emerging Technologies

How can scientists make gene editing techniques safer?

Tanya Lewis
Reporter, Business Insider
Share:
Our Impact
What's the World Economic Forum doing to accelerate action on Emerging Technologies?
A hand holding a looking glass by a lake
Crowdsource Innovation
Get involved with our crowdsourced digital platform to deliver impact at scale
Stay up to date:

Future of Global Health and Healthcare

Earlier this year, Chinese scientists made headlines when they used a gene-editing technique to modify the genomes of human embryos for the first time.

But the new technique, which has been called the “biggest biotech discovery of the century,” comes with side effects, including dangerous mutations, or genetic tweaks, that could result in disease or even death.

Now, scientists think they’ve found a way to prevent some of these unintended consequences, according to a new study published yesterday in the journal Human Gene Therapy.

To understand these consequences, first you have to understand the technique itself.

Known as CRISPR-Cas9, the technique is basically a way to “cut and paste” bits of DNA into a gene. It was discovered accidentally by Jennifer Doudna, a biochemist at the University of California, Berkeley, and her collaborator, Emmanuelle Charpentier of the Helmholtz Centre for Infection Research in Germany.

How gene editing works

Bacteria have been using this technique for millions of years to protect themselves from viruses. When they detect some of a virus’s DNA, they cut and paste it into their own genomes, so they can recognize the invaders next time they encounter them.

A few years ago, Doudna and her colleagues realized that this naturally occuring cut-and-paste process could be used to change the DNA sequence of any cell. This is a game changer: It means you could potentially cut out a faulty gene and replace it with a healthy version.

Unfortunately, the process can result in some genetic mutations, or tweaks in the order of the pairs that make up a strand of DNA. And even the tiniest of mutations can have deadly consequences: a mutation in a single gene can cause cystic fibrosis, a life-threatening disorder of the lungs and digestive system. Alternatively, the mutations could be beneficial. In these cases, scientists who want to cause a specific mutation could swap in the desired DNA sequence for the DNA that was cut out.

So far, the technique has been used in cows, pigs, monkeys, and, at least in one controversial recent study, humans.

Many researchers have expressed strong concerns about the ethics and safety of tinkering with human embryos, even though these particular embryos were chosen because they were unable to survive. For one thing, when the Chinese researchers used the technique, it produced far too many errors to be considered safe for medical use in humans.

A step toward making it safer?

Researchers at Harvard Medical School said this week that they’ve found a way to reduce the number of these unwanted mutations by 40%.

The study involved two kinds of human cells: cancer cells (which are important for their ability to grow and reproduce quickly and are often used for genetics studies) and embryonic stem cells (which are important for their ability to develop into any type of tissue and are useful for studying human development).

The process involves two key differences:

  1. First, the researchers used a special version of the Cas9 enzyme that binds to the DNA but can’t cut it. Because of this characteristic, the enzyme is said to be “dead.” To cut the DNA, they used another enzyme, called Fok1 nuclease, which consists of two pieces that bind together. This change makes it a much more accurate method for targeting a specific DNA sequence, the researchers write in their paper.
  2. Next, the researchers used shortened versions of the guide RNAs (the genetic strands that target a desired part of the genome) to find the DNA they wanted to modify. In their study, using these shorter RNAs still produced the desired changes in the DNA, but with fewer unwanted mutations.

To measure how accurate their method was, the team used a genetic sequencing technique they developed themselves which looks for unintended breaks in both strands of the DNA.

Even though the modified technique reduced a significant amount of unwanted mutations, there were still stray mutations in two parts of the DNA, the researchers noted.

Here’s a video that describes the basic gene-editing technique:

This article is published in collaboration with Business Insider. Publication does not imply endorsement of views by the World Economic Forum.

To keep up with the Agenda subscribe to our weekly newsletter.

Author: Tanya is a science reporter at Business Insider, specializing in the intersection between biology and tech.

Image: A mother smiles at her baby as they wait to board a train at a railway station in Hangzhou, eastern China’s Zhejiang province January 23, 2007. REUTERS/Lang Lang.

Don't miss any update on this topic

Create a free account and access your personalized content collection with our latest publications and analyses.

Sign up for free

License and Republishing

World Economic Forum articles may be republished in accordance with the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Public License, and in accordance with our Terms of Use.

The views expressed in this article are those of the author alone and not the World Economic Forum.

Share:
World Economic Forum logo
Global Agenda

The Agenda Weekly

A weekly update of the most important issues driving the global agenda

Subscribe today

You can unsubscribe at any time using the link in our emails. For more details, review our privacy policy.

This is how cities can unleash the electric vehicle transition

Adrienne Gibbs and Jamie Wylie

September 26, 2024

About Us

Events

Media

Partners & Members

  • Sign in
  • Join Us

Language editions

Privacy Policy & Terms of Service

Sitemap

© 2024 World Economic Forum