The role of the m6A/m demethylase FTO in memory is both task and sex-dependent in mice

• Published in: Neurobiology of learning and memory Vol. 210; p. 107903
• Main Authors: Leonetti, Amanda M., Galluzzo, Isabella R., McLean, Timothy A.D., Stefanelli, Gilda, Ramnaraign, Fiona, Holm, Samuel, Winston, Stephen M., Reeves, Isaiah L., Brimble, Mark A., Walters, Brandon J.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.04.2024
• Subjects: Epigenetics; Epitranscriptomics; Fto; Learning and Memory; m6A; RNA methylation; Fto; Epigenetics; m6A; Epitranscriptomics; Learning and Memory; RNA methylation
• DOI: 10.1016/j.nlm.2024.107903
• ISSN: 1074-7427

•Depleting FTO impaired object location match memory in male mice.•Depleting FTO had no effect on novel object memory in male mice.•Depleting FTO has no role in female novel object or object location memory.•Depletion of FTO has a anxiolytic effect on male mice only in the elevated plus maze. Formation of long-term memories requires learning-induced changes in both transcription and translation. Epitranscriptomic modifications of RNA recently emerged as critical regulators of RNA dynamics, whereby adenosine methylation (m6A) regulates translation, mRNA stability, mRNA localization, and memory formation. Prior work demonstrated a pro-memory phenotype of m6A, as loss of m6A impairs and loss of the m6A/m demethylase FTO improves memory formation. Critically, these experiments focused exclusively on aversive memory tasks and were only performed in male mice. Here we show that the task type and sex of the animal alter effects of m6A on memory, whereby FTO-depletion impaired object location memory in male mice, in contrast to the previously reported beneficial effects of FTO depletion on aversive memory. Additionally, we show that female mice have no change in performance after FTO depletion, demonstrating that sex of the mouse is a critical variable for understanding how m6A contributes to memory formation. Our study provides the first evidence for FTO regulation of non-aversive spatial memory and sexspecific effects of m6A, suggesting that identification of differentially methylated targets in each sex and task will be critical for understanding how epitranscriptomic modifications regulate memory.