TY - JOUR
T1 - Divergent landscapes of A-to-I editing in postmortem and living human brain
AU - Rodriguez de los Santos, Miguel
AU - Kopell, Brian H.
AU - Buxbaum Grice, Ariela
AU - Ganesh, Gauri
AU - Yang, Andy
AU - Amini, Pardis
AU - Liharska, Lora E.
AU - Vornholt, Eric
AU - Fullard, John F.
AU - Dong, Pengfei
AU - Park, Eric
AU - Zipkowitz, Sarah
AU - Kaji, Deepak A.
AU - Thompson, Ryan C.
AU - Liu, Donjing
AU - Park, You Jeong
AU - Cheng, Esther
AU - Ziafat, Kimia
AU - Moya, Emily
AU - Fennessy, Brian
AU - Wilkins, Lillian
AU - Silk, Hannah
AU - Linares, Lisa M.
AU - Sullivan, Brendan
AU - Cohen, Vanessa
AU - Kota, Prashant
AU - Feng, Claudia
AU - Johnson, Jessica S.
AU - Rieder, Marysia Kolbe
AU - Scarpa, Joseph
AU - Nadkarni, Girish N.
AU - Wang, Minghui
AU - Zhang, Bin
AU - Sklar, Pamela
AU - Beckmann, Noam D.
AU - Schadt, Eric E.
AU - Roussos, Panos
AU - Charney, Alexander W.
AU - Breen, Michael S.
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/12
Y1 - 2024/12
N2 - Adenosine-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 higher ADAR and ADARB1 expression, 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 offer more nuanced and accurate insights into the regulatory mechanisms of RNA editing in the human brain.
AB - Adenosine-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 higher ADAR and ADARB1 expression, 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 offer more nuanced and accurate insights into the regulatory mechanisms of RNA editing in the human brain.
UR - https://www.scopus.com/pages/publications/85197179118
U2 - 10.1038/s41467-024-49268-z
DO - 10.1038/s41467-024-49268-z
M3 - Article
C2 - 38926387
AN - SCOPUS:85197179118
SN - 2041-1723
VL - 15
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 5366
ER -