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Dyslexia gene may have been pinpointed

The condition has long been thought to have a genetic component and researchers may now have found a specific gene

DYSLEXIA has long been thought to have a genetic component. Now researchers may have pinpointed a specific dyslexia gene.

Jeffrey Gruen at Yale University and his colleagues genotyped 536 individuals from 153 nuclear families who had dyslexia. They scoured a region of chromosome 6 that was already associated with dyslexia and found a deletion in a gene called DCDC2, which is expressed in high levels in parts of the brain involved in reading.

Gruen’s team then studied the gene’s role during early development in “knockout” rats – ones in which the gene was deliberately impaired. They found that neural cells failed to migrate as they should (Proceedings of the National Academy of Sciences, DOI: 10.1073/pnas.0508591102).

“Connecting this to reading is a leap of faith,” says Gruen. “But it would make sense.” He suggests that genetic screening and early intervention might help overcome the disability.