Public awareness of the impact of autism has been increasing, but there are still many aspects of the disease that are poorly understood by doctors and scientists. Chinese researchers have made a breakthrough by finding the functions of an important gene in brain development, and that its deficiency can cause autism.
Autism spectrum disorder (ASD) has been recognized as a highly heritable brain developmental disorder. It is characterized by deficits in social communication and interactions, as well as stereotyped, repetitive behaviors and restricted interests.
Sh3rf2 is a protein coding gene. Previous studies showed that it is often expressed at high levels in tumor cells. Deletion mutation of Sh3rf2, which has lost one copy and is left with a single functional copy of the gene, has been detected in autistic patients.
However, the role of Sh3rf2 in brain function and the underlying mechanism of how it functions remains unknown.
In experiments done on mice, researchers from the Chinese Academy of Sciences and the Beijing Normal University deleted one copy of the Sh3rf2 and found that the mutation led to typical autism-related behaviors.
Mice with the mutation displayed hyperactive behaviors in their home cages, such as continuous jumping or fighting with litter mates, repetitive digging and spontaneous seizures.
Further study showed that the Sh3rf2 mutant could cause disturbances and abnormal neuronal structures and functions in the left-brain hemisphere.
The human brain is divided into two hemispheres, called the left and the right hemisphere. Each hemisphere provides a different set of functions, behaviors and controls. The right hemisphere is often called the creative side, while the left is logical side, essential for the function of language.
Failure to develop normal language comprehension is an early sign of autism. Accordingly, left hemisphere dysfunction is often seen in autistic patients, said Xu Zhiheng, lead author and researcher with the academy’s Institute of Genetics and Developmental Biology.