Study Shows Proof-of-Concept of Gene Editing in DMD
March 22, 2021
Rare Daily Staff
A team of researchers at The Hospital for Sick Children created a mouse model emulating the exact genetic mutation of a patient with Duchenne muscular dystrophy and used a CRISPR-Cas9 strategy that restored full functionality to the disease-causing gene.
The genome-editing technique could eventually be used in humans to treat almost 10 percent of all rare inherited disorders, the researchers said. Their findings were published online in EMBO Molecular Medicine.
The patient mutation the researchers re-created in the lab is called a duplication mutation. These mutations occur when a region of a chromosome or gene is repeated. Duplication mutations are thought to be the direct cause for almost 10 percent of rare inherited disorders. Yet, finding effective treatments has been hindered due to a lack of animal models that can accurately replicate these mutations.
To advance the development of novel therapeutics, preclinical studies conducted in animal models need to show the treatment’s safety and efficacy before research teams can proceed to clinical trials with patients.
“Precision medicine solutions, such as genome editing, have emerged as a beacon of hope for patients with rare genetic disorders such as Duchenne muscular dystrophy (DMD). While this research is charging ahead in some areas, it has been hampered for patients with duplication mutations,” says Ronald Cohn, principal investigator of the study, president and CEO, senior scientist, pediatrician and geneticist at SickKids. “Our research seeks to open up treatment avenues that we previously weren’t able to explore for these patients.”
Duplication mutations are difficult to re-create in the lab because scientists must add DNA, rather than take it away. Many different genetic events must occur correctly and at the same time in order to re-create these mutations.
Using CRISPR-Cas9 technology, the SickKids research team successfully re-created the patient’s distinct duplication mutation, effectively replicating the patient’s specific form of DMD in a mouse model.
DMD is a life-threatening, progressive, neuromuscular disorder and the only treatments currently available provide limited improvement in muscle function. DMD is caused by mutations within the dystrophin gene, which is one of the largest genes in the body. This gene makes the dystrophin protein, which is critical for strengthening muscles and protecting them from injury. Therapies that are studied for DMD often result in creating a ‘shorter’ dystrophin gene that can lessen the severity of symptoms but are not curative.
The research team wanted to restore the dystrophin gene to its full length, essentially recreating a normal gene. They applied a CRISPR-Cas9 strategy they developed in 2015. At the time, the strategy was successful when applied to patient cells in vitro but now they would be able to test the strategy for the first time in a living animal.
The researchers used CRISPR-Cas9 to target and remove the duplication, restoring the gene’s normal function and ability to make dystrophin. The mice were treated soon after birth and demonstrated a significant reduction in the severity and presence of DMD symptoms compared to untreated mice.
“Our work provides a proof-of-concept that CRISPR-Cas9 can be a powerful tool for both modelling and treating duplication mutations,” says Cohn, who is also a professor of pediatrics and molecular genetics at the University of Toronto. “This is a giant step forward, not just for patients with DMD, but for all those with duplication mutation disorders.”
Next, the researchers hope to test their strategy in older mice to see if they can not only prevent the development of DMD symptoms, but reverse symptoms that have already started.
Photo: Ronald Cohn, principal investigator of the study, president and CEO, senior scientist, pediatrician and geneticist at SickKids
Sign up for updates straight to your inbox.