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Autism spectrum disorder linked to mutations in some mitochondrial DNA

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Credit: Darryl Leja, NHGRI, Flickr

Children diagnosed with autism spectrum disorder (ASD) have greater numbers of harmful mutations in their mitochondrial DNA than family members, report Zhenglong Gu of Cornell University in Ithaca, New York, and colleagues, in a study published October 28th, 2016 in PLOS Genetics.

Increasingly, studies [1,2] point to malfunctions in mitochondria – the powerhouses of the cell – as a cause of autism spectrum disorder, but the biological basis for this relationship is unclear. To see if a genetic link exists between mitochondrial malfunction and ASD, the scientists analyzed mitochondrial DNA sequences from 903 children with ASD, along with their unaffected siblings and mothers. They discovered a unique pattern of heteroplasmic mutations, where both mutant and normal mitochondrial DNA sequences exist in a single cell. Children with ASD had more than twice as many potentially harmful mutations compared to unaffected siblings, and 1.5 times as many mutations that would alter the resulting protein. The researchers went on to show that these mutations can be inherited from the mother, or the result of spontaneous mutation during development.

The scientists noted that the risk associated with these mutations is most pronounced in children with lower IQ and poor social behavior compared to their unaffected siblings. Carrying harmful mutations in mitochondrial DNA is also associated with increased risk of neurological and developmental problems among children with ASD. Because mitochondria play a central role in metabolism, these findings may help explain the metabolic disorders commonly associated with ASD and other neurodevelopmental disorders. Evaluating mutations in the mitochondrial DNA of high-risk families could help improve the diagnosis and treatment of these diseases.

Zhenglong Gu says "The result of our study synergizes with recent work on ASD, calling attention to children diagnosed with ASD who have one or more developmental abnormalities or related co-morbid clinical conditions for further testing on mitochondrial DNA and mitochondrial function. Since many neurodevelopmental disorders and related childhood disorders show abnormalities that converge upon mitochondrial dysfunction, and may have mtDNA defects as a common harbinger, future research is needed to elucidate the mitochondrial mechanisms underpinning to these diseases. Ultimately, understanding the energetic aspects of neurodevelopmental disorders may lead to entirely new kinds of treatments, and preventative strategies that would target mitochondria."

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References

1. Rossignol DA, Frye RE. Mitochondrial dysfunction in autism spectrum disorders?: a systematic review and meta-analysis. Mol Psychiatry. Nature Publishing Group; 2011;17: 290-314. doi:10.1038/mp.2010.136
2. Goh S, Dong Z, Zhang Y, DiMauro S, Peterson BS. Mitochondrial dysfunction as a neurobiological subtype of autism spectrum disorder: evidence from brain imaging. JAMA psychiatry. 2014;71: 665-71. doi:10.1001/jamapsychiatry.2014.179

In your coverage please use this URL to provide access to the freely available article in PLOS Genetics: http://dx.doi.org/10.1371/journal.pgen.1006391

Citation: Wang Y, Picard M, Gu Z (2016) Genetic Evidence for Elevated Pathogenicity of Mitochondrial DNA Heteroplasmy in Autism Spectrum Disorder. PLoS Genet 12(10): e1006391. doi:10.1371/journal.pgen.1006391

Funding: This work was supported by various funds from Cornell University, NSF MCB-1243588, NIH 1R01AI085286, and a grant for ENN science and technology development to ZG. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Competing Interests: The authors have declared that no competing interests exist.

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Zhenglong Gu
[email protected]

http://www.plos.org

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