Divergent landscapes of A-to-I editing in postmortem and living human brain

Author:

Rodriguez de los Santos MiguelORCID,Kopell Brian H.,Buxbaum Grice Ariela,Ganesh Gauri,Yang Andy,Amini Pardis,Liharska Lora E.,Vornholt Eric,Fullard John F.,Dong Pengfei,Park Eric,Zipkowitz Sarah,Kaji Deepak A.,Thompson Ryan C.,Liu Donjing,Park You Jeong,Cheng Esther,Ziafat Kimia,Moya Emily,Fennessy Brian,Wilkins Lillian,Silk Hannah,Linares Lisa M.,Sullivan Brendan,Cohen Vanessa,Kota Prashant,Feng Claudia,Johnson Jessica S.,Rieder Marysia-Kolbe,Scarpa Joseph,Nadkarni Girish N.,Wang Minghui,Zhang Bin,Sklar Pamela,Beckmann Noam D.,Schadt Eric E.,Roussos Panos,Charney Alexander W.,Breen Michael S.ORCID

Abstract

ABSTRACTAdenosine-to-inosine (A-to-I) editing is a prevalent post-transcriptional RNA modification within the brain. Yet, most research has relied on postmortem samples, assuming it is an accurate representation of RNA biology in the living brain. We challenge this assumption by comparing A-to-I editing between postmortem and living prefrontal cortical tissues. Major differences were found, with over 70,000 A-to-I sites showing higher editing levels in postmortem tissues. Increased A-to-I editing in postmortem tissues is linked to higherADAR1andADARB1expression, is more pronounced in non-neuronal cells, and indicative of postmortem activation of inflammation and hypoxia. Higher A-to-I editing in living tissues marks sites that are evolutionarily preserved, synaptic, developmentally timed, and disrupted in neurological conditions. Common genetic variants were also found to differentially affect A-to-I editing levels in living versus postmortem tissues. Collectively, these discoveries illuminate the nuanced functions and intricate regulatory mechanisms of RNA editing within the human brain.

Publisher

Cold Spring Harbor Laboratory

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