Global analysis of excitotoxicity-induced alterations in RNA structure and RNA-protein binding in neurons

Excitotoxicity and altered RNA regulation by RNA-binding proteins (RBPs) are two prevalent hallmarks in multiple neurodegenerative disorders. However, global effects of excitotoxicity on RNA secondary structure and RNA-protein interactions are largely unknown. To address this, we have performed protein interaction profile sequencing (PIP-seq) in NMDA-treated primary neurons. Our results show that NMDA treatment alters RNA structure, which correlates, in opposite directions depending on the intragenic region, with changes in mRNA abundance. Moreover, NMDA treatment increases and alters RNA-protein binding sites defining subsets of transcripts functionally associated with synaptic functions and neurodegenerative disorders. Finally, we identify two RNA motifs enriched in protein binding after NMDA treatment, and several RBPs binding to them <i>in vitro</i>, including CELF6 and YBX3, which show NMDA-dependent changes in their protein levels. Overall, we provide extensive datasets that can be leveraged to bridge the mechanistic gap between two hallmarks of neurodegeneration: excitotoxicity and RNA regulation by RBPs.

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Publication Details

Journal
iScience
Published
2025-05-06
DOI
https://doi.org/10.1016/j.isci.2025.112595
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
0.00

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article

Global analysis of excitotoxicity-induced alterations in RNA structure and RNA-protein binding in neurons

Brian D. Gregory, Elena Alvarez-Periel, Marianne C. Kramer, Cagla Akay et al.
iScience
RNA Research and Splicing
article

Global analysis of excitotoxicity-induced alterations in RNA structure and RNA-protein binding in neurons

Brian D. Gregory, Elena Alvarez-Periel, Marianne C. Kramer, Cagla Akay, Kelly L. Jordan‐Sciutto, Benjamin Aaron Garcia, D. Paul Jackson, Julia A Tasca
article en

Abstract

Excitotoxicity and altered RNA regulation by RNA-binding proteins (RBPs) are two prevalent hallmarks in multiple neurodegenerative disorders. However, global effects of excitotoxicity on RNA secondary structure and RNA-protein interactions are largely unknown. To address this, we have performed protein interaction profile sequencing (PIP-seq) in NMDA-treated primary neurons. Our results show that NMDA treatment alters RNA structure, which correlates, in opposite directions depending on the intragenic region, with changes in mRNA abundance. Moreover, NMDA treatment increases and alters RNA-protein binding sites defining subsets of transcripts functionally associated with synaptic functions and neurodegenerative disorders. Finally, we identify two RNA motifs enriched in protein binding after NMDA treatment, and several RBPs binding to them <i>in vitro</i>, including CELF6 and YBX3, which show NMDA-dependent changes in their protein levels. Overall, we provide extensive datasets that can be leveraged to bridge the mechanistic gap between two hallmarks of neurodegeneration: excitotoxicity and RNA regulation by RBPs.

iScienceVol. 28(6)
University of Pennsylvania (US)
National Institutes of Health, National Institute of Mental Health, National Institute on Drug Abuse, National Institute of Allergy and Infectious Diseases, National Institute of Neurological Disorders and Stroke, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Zero hunger
Openalex Percentile: Top 91%
RNA Research and Splicing
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