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bioRxiv · 10.1101/2020.03.03.975722

Network signature of complement component 4 variation in the human brain identifies convergent molecular risk for schizophrenia

Kim, M.·Haney, J. R.·Zhang, P.·Hernandez, L. M.·Wang, L.-k.·Perez-Cano, L.·Gandal, M. J.
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Abstract

The most significant common variant association for schizophrenia (SCZ) reflects increased expression of the complement component 4A (C4A). Yet, it remains unclear how C4A interacts with other SCZ risk genes and whether the complement system is more broadly implicated in SCZ pathogenesis. Here, we integrate several existing, large-scale genetic and transcriptomic datasets to interrogate the functional role of the complement system and C4A in the human brain. Surprisingly, we find no significant genetic enrichment among known complement system genes for SCZ. Conversely, brain co-expression network analyses using C4A as a seed gene revealed that genes down-regulated when C4A expression increased exhibit strong and specific genetic enrichment for SCZ risk. This convergent genomic signal reflected neuronal, synaptic processes and was sexually dimorphic and most prominent in frontal cortical brain regions. Overall, these results indicate that synaptic pathways--rather than the complement system--are the driving force conferring SCZ risk.

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Kim, M., Haney, J. R., Zhang, P., Hernandez, L. M., Wang, L.-k., Perez-Cano, L., Gandal, M. J.. 2020-03-04. Network signature of complement component 4 variation in the human brain identifies convergent molecular risk for schizophrenia. https://doi.org/10.1101/2020.03.03.975722

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