{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Ninochka D'Souza M"],"funding":["DST Swarnajayanti Fellowship","Centre for Brain Researc","National Postdoctoral Fellowship from DST","SERB-DST"],"pagination":["1-22"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC12498540"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["22(1)"],"pubmed_abstract":["The Fragile X Messenger Ribonucleoprotein (FMRP) is a selective RNA-binding protein that localizes to the cytoplasm and the nucleus. The loss of FMRP results in Fragile X Syndrome (FXS), an autism spectrum disorder. FMRP interacts with ribosomes and regulates the translation of mRNAs essential for neuronal development and synaptic plasticity. However, the biochemical nature of this translation regulation is unknown. Here, we report that a potential feature of FMRP-mediated translation regulation during neuronal differentiation is the modulation of 2'-O-methylation of ribosomal RNA. 2'O-methylation, facilitated by C/D box snoRNAs in the nucleus, is a major epitranscriptome mark on rRNA, essential for ribosome assembly and function. We found that FMRP influences a distinct rRNA 2'O-Methylati"],"journal":["RNA biology"],"pubmed_title":["Altering rRNA 2'O-methylation pattern during neuronal differentiation is regulated by FMRP."],"pmcid":["PMC12498540"],"funding_grant_id":["EMR/2016/006313","DST/SJF/LSA-02/2015–16","PDF/2018/000663"],"pubmed_authors":["Muddashetty RS","Palakodeti D","Ninochka D'Souza M","Hariharan N","Gowda NKC","Qadri SW"],"additional_accession":[]},"is_claimable":false,"name":"Altering rRNA 2'O-methylation pattern during neuronal differentiation is regulated by FMRP.","description":"The Fragile X Messenger Ribonucleoprotein (FMRP) is a selective RNA-binding protein that localizes to the cytoplasm and the nucleus. The loss of FMRP results in Fragile X Syndrome (FXS), an autism spectrum disorder. FMRP interacts with ribosomes and regulates the translation of mRNAs essential for neuronal development and synaptic plasticity. However, the biochemical nature of this translation regulation is unknown. Here, we report that a potential feature of FMRP-mediated translation regulation during neuronal differentiation is the modulation of 2'-O-methylation of ribosomal RNA. 2'O-methylation, facilitated by C/D box snoRNAs in the nucleus, is a major epitranscriptome mark on rRNA, essential for ribosome assembly and function. We found that FMRP influences a distinct rRNA 2'O-Methylati","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Dec","modification":"2026-05-05T03:15:43.14Z","creation":"2026-05-05T03:12:44.801Z"},"accession":"S-EPMC12498540","cross_references":{"pubmed":["41042002"],"doi":["10.1080/15476286.2025.2563986"]}}