CRISPR fix for hearing
Scientists in the US and China have successfully restored hearing in a mouse model of human genetic deafness.
The paper published in Nature highlights the promise of CRISPR–Cas9 as a potential strategy for treating some dominantly inherited hearing-loss diseases.
Genetic factors contribute to nearly half of all deafness cases, yet there are limited treatment options available for inherited hearing loss.
A research team featuring experts from the US and China have designed a lipid-encapsulated Cas9–guide RNA complex that can specifically target a deafness-causing genetic mutation in a mouse model of human deafness.
They show that the system can disrupt the deafness-causing mutant gene, even though it differs from the healthy gene by only one base pair.
They also showed that injecting the complex into the cochlea of neonatal mice substantially reduces progressive hearing loss.
The authors observed higher hair cell survival rates and lower auditory brainstem response thresholds in injected ears compared with uninjected ears or ears injected with complexes that target an unrelated gene.
They also observed better acoustic reflex responses in injected compared to uninjected mice.
The authors conclude that this genome-editing strategy may contribute to the future development of a DNA- and virus-free, one-time treatment for certain genetic hearing-loss disorders.