Involvement of phosphodiesterase 2A activity in the pathophysiology of fragile X syndrome

T Maurin, F Melancia, M Jarjat, L Castro, L Costa…�- Cerebral�…, 2019 - academic.oup.com
The fragile X mental retardation protein (FMRP) is an RNA-binding protein involved in
translational regulation of mRNAs that play key roles in synaptic morphology and plasticity�…

[HTML][HTML] Dynamic FMR1 granule phase switch instructed by m6A modification contributes to maternal RNA decay

G Zhang, Y Xu, X Wang, Y Zhu, L Wang…�- Nature�…, 2022 - nature.com
Maternal RNA degradation is critical for embryogenesis and is tightly controlled by maternal
RNA-binding proteins. Fragile X mental-retardation protein (FMR1) binds target mRNAs to�…

N6-Methyladenosine mRNA Modification: From Modification Site Selectivity to Neurological Functions

Z Zhang, XJ Wang�- Accounts of Chemical Research, 2023 - ACS Publications
Conspectus The development of various chemical methods has enabled scientists to
decipher the distribution features and biological functions of RNA modifications in the past�…

O-GlcNAcylation determines the translational regulation and phase separation of YTHDF proteins

Y Chen, R Wan, Z Zou, L Lao, G Shao, Y Zheng…�- Nature Cell�…, 2023 - nature.com
Abstract N 6-methyladenosine (m6A) is the most abundant internal mRNA nucleotide
modification in mammals, regulating critical aspects of cell physiology and differentiation�…

N6-methyladenosine–encoded epitranscriptomics

N Liu, T Pan�- Nature structural & molecular biology, 2016 - nature.com
Abstract N 6-methyladenosine (m 6 A) is the most abundant internal modification in
eukaryotic mRNA. Recent discoveries of the locations, functions and mechanisms of m 6 A�…

[HTML][HTML] Enhanced expression of ADCY1 underlies aberrant neuronal signalling and behaviour in a syndromic autism model

F Sethna, W Feng, Q Ding, AJ Robison, Y Feng…�- Nature�…, 2017 - nature.com
Fragile X syndrome (FXS), caused by the loss of functional FMRP, is a leading cause of
autism. Neurons lacking FMRP show aberrant mRNA translation and intracellular signalling�…

[HTML][HTML] Deciphering the “m6A code” via antibody-independent quantitative profiling

MA Garcia-Campos, S Edelheit, U Toth, M Safra…�- Cell, 2019 - cell.com
Summary N6-methyladenosine (m 6 A) is the most abundant modification on mRNA and is
implicated in critical roles in development, physiology, and disease. A major limitation has�…

[HTML][HTML] Regulatory Mechanisms of the RNA Modification m6A and Significance in Brain Function in Health and Disease

J Mathoux, DC Henshall, GP Brennan�- Frontiers in cellular�…, 2021 - frontiersin.org
RNA modifications have emerged as an additional layer of regulatory complexity governing
the function of almost all species of RNA. N 6-methyladenosine (m6A), the addition of methyl�…

N6-methyladenosine regulates maternal RNA maintenance in oocytes and timely RNA decay during mouse maternal-to-zygotic transition

Y Wu, X Xu, M Qi, C Chen, M Li, R Yan, X Kou…�- Nature cell�…, 2022 - nature.com
Abstract N 6-methyladenosine (m6A) and its regulatory components play critical roles in
various developmental processes in mammals. However, the landscape and function of�…

[HTML][HTML] RNA m6A methylation participates in regulation of postnatal development of the mouse cerebellum

C Ma, M Chang, H Lv, ZW Zhang, W Zhang, X He…�- Genome biology, 2018 - Springer
Abstract Background N 6-methyladenosine (m 6 A) is an important epitranscriptomic mark
with high abundance in the brain. Recently, it has been found to be involved in the�…