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This is an archive article published on June 27, 2018

Gene editing can curb autism symptoms

A research team is believed to be the first to successfully edit a causal gene for autism in the brain, and edited it to reduce the impact of the motor neuron disease.

Autism gene edited, CRISPR-Cas9 gene, University of Texas San Antonio, CRISPR-Gold, autism spectrum disorders, DNA cutting, biochemical reactions, neuron communications The approach can also be used to treat other diseases including many neurological diseases. (Image: University of Texas Health Science Center at San Antonio)

Scientists have found that editing a gene in the brain can help decrease the repetitive behaviours – a symptom of autism spectrum disorders. In the study, the team led by scientists at University of Texas-San Antonio, used nanoparticle carriers to inject a gene-editing enzyme called Cas9 into the striatum – a brain region associated with formation of habits. Enzymes are proteins that trigger biochemical reactions.

“The enzyme we used, Cas9, is like a pair of scissors. We were able to cut the genetic blueprint, DNA, at a location that causes the exaggerated repetitive behaviours,” said Hye Young Lee, Assistant Professor at the varsity.

In a mice model with fragile X syndrome – an inherited cause of autism spectrum disorders, the researchers targeted Cas9 at a molecule called mGluR5 that is excitatory – it increases communications between neurons. The approach worked. The rodents’ digging behaviour slowed by 30 per cent and the leaping behaviour was reduced by 70 per cent, Lee said, in the paper described in the journal Nature Biomedical Engineering.

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The team is believed to be the first to successfully edit a causal gene for autism in the brain and diminish symptoms. Significantly, the effect is permanent, Lee said. “The approach can also be used to treat other diseases including many neurological diseases such as epilepsy, and the brain cancer glioblastoma, if we know the gene target,” she said.

 

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