How a Zebrafish Could Help Solve the Mysteries of Genetic Brain Disease

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A close look at the rapidly developing zebrafish embryo is helping neuroscientists better understand the potential underpinnings of brain disorders, including autism and schizophrenia.

A close look at the rapidly developing zebrafish embryo is helping neuroscientists better understand the potential underpinnings of brain disorders, including autism and schizophrenia.

Researchers at The Ohio State University were interested in understanding changes in neurological development that arise from a genetic defect associated with neurological disease – specifically, the loss of a gene called Protocadherin-19, or PCDH19. The link between the mutation and brain disorders is well-established, but the mechanics of why one might lead to the other have been a mystery.

The new study, published online this month in the journal eNeuro, points to a “clustering” of cellular interactions in the brain that may disrupt normal development and brain health.

“Scientists have discovered hundreds of genes that give rise to schizophrenia, autism and other brain disorders, but nobody knows what specifically goes wrong as a result of these genetic mutations,” said lead researcher James Jontes, an associate professor of neuroscience at Ohio State and member of the university’s Neurological Institute.

Read more at Ohio State University