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Mutation in mitochondrial chaperone TRAP1 results in male-specific autism

Rydzanicz, M.; Kuzniewska, B.; Magnowska, M.; Wojtowicz, T.; Borsuk, E.; Gewartowska, O.; Gruchota, J.; Hojka, A.; Milek, J.; Stawikowska, A.; Wardaszka, P.; Chojnicka, I.; Kondrakiewicz, L.; Puscian, A.; Knapska, E.; Dziembowski, A.; Ploski, R.; Dziembowska, M.

2023-06-06 neuroscience
10.1101/2023.06.02.543381 bioRxiv
Show abstract

There is increasing evidence of mitochondrial dysfunction in autism spectrum disorders (ASD), but the causal relationships are unclear. In an ASD patient whose identical twin was unaffected, we identified a postzygotic mosaic mutation p.Q639* in the TRAP1 gene, which encodes a mitochondrial chaperone of the HSP90 family. Additional screening of 176 unrelated ASD probands revealed an identical TRAP1 variant in a male patient who had inherited it from a healthy mother. Notably, newly generated knock-in Trap1 p.Q641* mice display ASD-related behavioral abnormalities exclusively in males. Accordingly, Trap1 p.Q641* mutation also resulted in sex-specific changes in synaptic plasticity, number of presynaptic mitochondria, and metabolic substrate consumption. Thus, the TRAP1 p.Q639* mutation is the first example of a monogenic ASD caused by impaired mitochondrial protein homeostasis. One-Sentence SummaryPatient mutation in TRAP1 causes autism in male mice.

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