دورية أكاديمية

Altered m6A RNA methylation contributes to hippocampal memory deficits in Huntington's disease mice.

التفاصيل البيبلوغرافية
العنوان: Altered m6A RNA methylation contributes to hippocampal memory deficits in Huntington's disease mice.
المؤلفون: Pupak, Anika, Singh, Ankita, Sancho Balsells, Anna, Alcalá Vida, Rafael, Espina, Marc, Giralt Coll, Albert, Martí Puig, Eulàlia, Vang Ørom, Ulf Andersson, Ginés Padrós, Silvia, Brito, Verónica
المصدر: Articles publicats en revistes (Biomedicina)
بيانات النشر: Springer Verlag
سنة النشر: 2022
المجموعة: Dipòsit Digital de la Universitat de Barcelona
مصطلحات موضوعية: Expressió gènica, Hipocamp (Cervell), Corea de Huntington, Trastorns de la memòria, RNA, Gene expression, Hippocampus (Brain), Huntington's chorea, Memory disorders
الوصف: N6-methyladenosine (m6A) regulates many aspects of RNA metabolism and is involved in learning and memory processes. Yet, the impact of a dysregulation of post-transcriptional m6A editing on synaptic impairments in neurodegenerative disorders remains unknown. Here we investigated the m6A methylation pattern in the hippocampus of Huntington's disease (HD) mice and the potential role of the m6A RNA modification in HD cognitive symptomatology. m6A modifications were evaluated in HD mice subjected to a hippocampal cognitive training task through m6A immunoprecipitation sequencing (MeRIP-seq) and the relative levels of m6A-modifying proteins (FTO and METTL14) by subcellular fractionation and Western blot analysis. Stereotaxic CA1 hippocampal delivery of AAV-shFTO was performed to investigate the effect of RNA m6A dysregulation in HD memory deficits. Our results reveal a m6A hypermethylation in relevant HD and synaptic related genes in the hippocampal transcriptome of Hdh+/Q111 mice. Conversely, m6A is aberrantly regulated in an experience-dependent manner in the HD hippocampus leading to demethylation of important components of synapse organization. Notably, the levels of RNA demethylase (FTO) and methyltransferase (METTL14) were modulated after training in the hippocampus of WT mice but not in Hdh+/Q111 mice. Finally, inhibition of FTO expression in the hippocampal CA1 region restored memory disturbances in symptomatic Hdh+/Q111 mice. Altogether, our results suggest that a differential RNA methylation landscape contributes to HD cognitive symptoms and uncover a role of m6A as a novel hallmark of HD.
نوع الوثيقة: article in journal/newspaper
وصف الملف: 21 p.; application/pdf
اللغة: English
تدمد: 1420-682X
العلاقة: Reproducció del document publicat a: https://doi.org/10.1007/s00018-022-04444-6Test; Cellular and Molecular Life Sciences, 2022, vol. 79, num. 8; https://doi.org/10.1007/s00018-022-04444-6Test; http://hdl.handle.net/2445/193337Test; 729396
الإتاحة: https://doi.org/10.1007/s00018-022-04444-6Test
http://hdl.handle.net/2445/193337Test
حقوق: cc-by (c) Pupak, Anika et al, 2022 ; http://creativecommons.org/licenses/by/3.0/esTest/ ; info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.56F96161
قاعدة البيانات: BASE