NSun2-Mediated Cytosine-5 Methylation of Vault Noncoding RNA Determines Its Processing into Regulatory Small RNAs
Wellcome/MRC Cambridge Stem Cell Institute · University of Cambridge · +6 more institutions
Abstract
Autosomal-recessive loss of the NSUN2 gene has been identified as a causative link to intellectual disability disorders in humans. NSun2 is an RNA methyltransferase modifying cytosine-5 in transfer RNAs (tRNAs), yet the identification of cytosine methylation in other RNA species has been hampered by the lack of sensitive and reliable molecular techniques. Here, we describe miCLIP as an additional approach for identifying RNA methylation sites in transcriptomes. miCLIP is a customized version of the individual-nucleotide-resolution crosslinking and immunoprecipitation (iCLIP) method. We confirm site-specific methylation in tRNAs and additional messenger and noncoding RNAs (ncRNAs). Among these, vault ncRNAs…
Citation impact
- FWCI
- 13.46
- Percentile
- 100%
- References
- 41
Authors
11- SHShobbir HussainCorresponding
Wellcome/MRC Cambridge Stem Cell Institute, University of Cambridge, Medical Research Council
- AAAbdulrahim A. Sajini
Wellcome/MRC Cambridge Stem Cell Institute, University of Cambridge, Medical Research Council
- SBSandra Blanco
Wellcome/MRC Cambridge Stem Cell Institute, University of Cambridge, Medical Research Council
- SDSabine Dietmann
Wellcome/MRC Cambridge Stem Cell Institute, University of Cambridge, Medical Research Council
- PLPatrick Lombard
Wellcome/MRC Cambridge Stem Cell Institute, University of Cambridge, Medical Research Council
Topics & keywords
- Biology
- Non-coding RNA
- RNA
- Small RNA
- Methylation
- Small nucleolar RNA
- microRNA
- Transfer RNA
- Good health and well-being