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Researchers have identified deletions in SHANK1 — the third member of a gene family that is closely linked to autism — in five men with the disorder, they reported 4 May in the American Journal of Human Genetics. This is the first study linking SHANK1 mutations to people with autism1.
In the new study, researchers looked for copy number variations — duplications or deletions of regions of DNA — in 1,614 individuals with autism and 15,127 controls. They found deletions in SHANK1 in two men with autism, but none of the controls.
One of these men inherited the deletion: Three of his male relatives also have the deletion, and have a diagnosis of high-functioning autism or autism-like symptoms, dubbed the broad autism phenotype. By contrast, two female relatives who have the deletion do not have symptoms of the disorder. The results support the theory that protective factors raise the threshold for autism risk in women compared with men, the researchers say.
The researchers also sequenced SHANK1 in 509 people with autism and 340 people with intellectual disability to look for single-letter DNA changes. They found 26 missense mutations, which alter the protein code, in 23 people with autism and 7 people with intellectual disability, but none in 285 controls. However, only two of these mutations are likely to affect the overall structure of the protein.
Mutations in SHANK1 may increase autism risk, but less so than SHANK2 and SHANK3, which are strongly linked to the disorder, the researchers say. This is consistent with SHANK1’s role at neuronal junctions, which is to support connections formed by the other SHANK proteins.
1: Sato D. et al. Am. J. Hum. Genet. 90, 879-887 (2012) PubMed