Yale scientists have discovered an underlying mechanism for Fragile X syndrome — a leading cause of autism and the primary genetic driver of intellectual disability — as well as a drug that reversed the underlying abnormality and autism-like behaviours in mice. Their research appears in the Sept. 3 edition of the journal Cell.

The new Yale study deepens basic understanding of the syndrome and demonstrates early promise for a previously unexplored avenue for treatment. 

In the study, led by Dr. Elizabeth Ann Jonas, professor of internal medicine (endocrinology) and neuroscience, researchers focused on a protein called adenosine triphosphate synthase, which is present in nearly all cells in the body. It uses energy from food to generate adenosine triphosphate (ATP), a molecule that is a major energy source for cells.

In Fragile X syndrome, cells’ ATP-making function is abnormal, Jonas’ team found. Specifically, the cells’ mitochondria — which process fuel to make ATP — have a leaky inner membrane. 

This leaky membrane is making the process of ATP production inefficient, In Fragile X neurons, the synapses fail to mature during development. The synapses remain in an immature state and this seems to be related to their immature metabolism. When a leak in the cell’s mitochondria short-circuits efficient functioning of the synapse, memory, learning and typical brain development are all compromised,
Dr. Elizabeth Ann Jonas

Jonas said she is now interested in testing the effectiveness of this and other leak-closing drugs for improving learning. She has a separate study underway intended to ascertain the role of leaky membranes in memory formation. This could yield a pathway for treating Alzheimer’s disease as well as for Fragile X and autism.

Mitochondria are making ATP in synapses all throughout life. We think mitochondrial leak closure may be one of the first responses to neuronal activity when you form a memory and this could be required for the changes that lead to long-term memory formation</cite<
Dr. Elizabeth Ann Jonas



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