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Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development

Posttranscriptional RNA modifications by adenosine-to-inosine (A-to-I) editing are abundant in the brain, yet elucidating functional sites remains challenging. To bridge this gap, we investigate spatiotemporal and genetically regulated A-to-I editing sites across prenatal and postnatal stages of hum...

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Autores principales: Cuddleston, Winston H., Fan, Xuanjia, Sloofman, Laura, Liang, Lindsay, Mossotto, Enrico, Moore, Kendall, Zipkowitz, Sarah, Wang, Minghui, Zhang, Bin, Wang, Jiebiao, Sestan, Nenad, Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J., Buxbaum, Joseph D., Breen, Michael S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9704047/
https://www.ncbi.nlm.nih.gov/pubmed/36323256
http://dx.doi.org/10.1016/j.celrep.2022.111585
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author Cuddleston, Winston H.
Fan, Xuanjia
Sloofman, Laura
Liang, Lindsay
Mossotto, Enrico
Moore, Kendall
Zipkowitz, Sarah
Wang, Minghui
Zhang, Bin
Wang, Jiebiao
Sestan, Nenad
Devlin, Bernie
Roeder, Kathryn
Sanders, Stephan J.
Buxbaum, Joseph D.
Breen, Michael S.
author_facet Cuddleston, Winston H.
Fan, Xuanjia
Sloofman, Laura
Liang, Lindsay
Mossotto, Enrico
Moore, Kendall
Zipkowitz, Sarah
Wang, Minghui
Zhang, Bin
Wang, Jiebiao
Sestan, Nenad
Devlin, Bernie
Roeder, Kathryn
Sanders, Stephan J.
Buxbaum, Joseph D.
Breen, Michael S.
author_sort Cuddleston, Winston H.
collection PubMed
description Posttranscriptional RNA modifications by adenosine-to-inosine (A-to-I) editing are abundant in the brain, yet elucidating functional sites remains challenging. To bridge this gap, we investigate spatiotemporal and genetically regulated A-to-I editing sites across prenatal and postnatal stages of human brain development. More than 10,000 spatiotemporally regulated A-to-I sites were identified that occur predominately in 3′ UTRs and introns, as well as 37 sites that recode amino acids in protein coding regions with precise changes in editing levels across development. Hyper-edited transcripts are also enriched in the aging brain and stabilize RNA secondary structures. These features are conserved in murine and non-human primate models of neurodevelopment. Finally, thousands of cis-editing quantitative trait loci (edQTLs) were identified with unique regulatory effects during prenatal and postnatal development. Collectively, this work offers a resolved atlas linking spatiotemporal variation in editing levels to genetic regulatory effects throughout distinct stages of brain maturation.
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spelling pubmed-97040472022-11-28 Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development Cuddleston, Winston H. Fan, Xuanjia Sloofman, Laura Liang, Lindsay Mossotto, Enrico Moore, Kendall Zipkowitz, Sarah Wang, Minghui Zhang, Bin Wang, Jiebiao Sestan, Nenad Devlin, Bernie Roeder, Kathryn Sanders, Stephan J. Buxbaum, Joseph D. Breen, Michael S. Cell Rep Article Posttranscriptional RNA modifications by adenosine-to-inosine (A-to-I) editing are abundant in the brain, yet elucidating functional sites remains challenging. To bridge this gap, we investigate spatiotemporal and genetically regulated A-to-I editing sites across prenatal and postnatal stages of human brain development. More than 10,000 spatiotemporally regulated A-to-I sites were identified that occur predominately in 3′ UTRs and introns, as well as 37 sites that recode amino acids in protein coding regions with precise changes in editing levels across development. Hyper-edited transcripts are also enriched in the aging brain and stabilize RNA secondary structures. These features are conserved in murine and non-human primate models of neurodevelopment. Finally, thousands of cis-editing quantitative trait loci (edQTLs) were identified with unique regulatory effects during prenatal and postnatal development. Collectively, this work offers a resolved atlas linking spatiotemporal variation in editing levels to genetic regulatory effects throughout distinct stages of brain maturation. 2022-11-01 /pmc/articles/PMC9704047/ /pubmed/36323256 http://dx.doi.org/10.1016/j.celrep.2022.111585 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Cuddleston, Winston H.
Fan, Xuanjia
Sloofman, Laura
Liang, Lindsay
Mossotto, Enrico
Moore, Kendall
Zipkowitz, Sarah
Wang, Minghui
Zhang, Bin
Wang, Jiebiao
Sestan, Nenad
Devlin, Bernie
Roeder, Kathryn
Sanders, Stephan J.
Buxbaum, Joseph D.
Breen, Michael S.
Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development
title Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development
title_full Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development
title_fullStr Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development
title_full_unstemmed Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development
title_short Spatiotemporal and genetic regulation of A-to-I editing throughout human brain development
title_sort spatiotemporal and genetic regulation of a-to-i editing throughout human brain development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9704047/
https://www.ncbi.nlm.nih.gov/pubmed/36323256
http://dx.doi.org/10.1016/j.celrep.2022.111585
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