RNA modifications in cancer

Q Tang, L Li, Y Wang, P Wu, X Hou, J Ouyang… - British journal of …, 2023 - nature.com
Currently, more than 170 modifications have been identified on RNA. Among these RNA
modifications, various methylations account for two-thirds of total cases and exist on almost …

Epitranscriptome sequencing technologies: decoding RNA modifications

X Li, X **ong, C Yi - Nature methods, 2017 - nature.com
In recent years, major breakthroughs in RNA-modification-mediated regulation of gene
expression have been made, leading to the emerging field of epitranscriptomics. Our …

A synaptic perspective of fragile X syndrome and autism spectrum disorders

C Bagni, RS Zukin - Neuron, 2019 - cell.com
Altered synaptic structure and function is a major hallmark of fragile X syndrome (FXS),
autism spectrum disorders (ASDs), and other intellectual disabilities (IDs), which are …

Functional diversity of small nucleolar RNAs

T Bratkovič, J Božič, B Rogelj - Nucleic acids research, 2020 - academic.oup.com
Small nucleolar RNAs (snoRNAs) are short non-protein-coding RNAs with a long-
recognized role in tuning ribosomal and spliceosomal function by guiding ribose methylation …

Nm-seq maps 2′-O-methylation sites in human mRNA with base precision

Q Dai, S Moshitch-Moshkovitz, D Han, N Kol… - Nature …, 2017 - nature.com
The ribose of RNA nucleotides can be 2′-O-methylated (Nm). Despite advances in high-
throughput detection, the inert chemical nature of Nm still limits sensitivity and precludes …

Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics

C Bagni, F Tassone, G Neri… - The Journal of clinical …, 2012 - Am Soc Clin Investig
Fragile X syndrome (FXS) is the most frequent form of inherited intellectual disability and is
also linked to other neurologic and psychiatric disorders. FXS is caused by a triplet …

RNA 2′-O-methylation (Nm) modification in human diseases

DG Dimitrova, L Teysset, C Carré - Genes, 2019 - mdpi.com
Nm (2′-O-methylation) is one of the most common modifications in the RNA world. It has
the potential to influence the RNA molecules in multiple ways, such as structure, stability …

The pathophysiology of fragile X (and what it teaches us about synapses)

AL Bhakar, G Dölen, MF Bear - Annual review of neuroscience, 2012 - annualreviews.org
Fragile X is the most common known inherited cause of intellectual disability and autism,
and it typically results from transcriptional silencing of FMR1 and loss of the encoded …

Structure and function of noncanonical nucleobases

T Carell, C Brandmayr, A Hienzsch… - Angewandte Chemie …, 2012 - Wiley Online Library
DNA and RNA contain, next to the four canonical nucleobases, a number of modified
nucleosides that extend their chemical information content. RNA is particularly rich in …

The emerging field of epitranscriptomics in neurodevelopmental and neuronal disorders

MT Angelova, DG Dimitrova, N Dinges… - … in bioengineering and …, 2018 - frontiersin.org
Analogous to DNA methylation and histone modifications, RNA modifications represent a
novel layer of regulation of gene expression. The dynamic nature and increasing number of …