Literature DB >> 34085245

Assessing 2'-O-Methylation of mRNA Using Quantitative PCR.

Brittany A Elliott1, Christopher L Holley2.   

Abstract

2'-O-methylation (Nm) is an RNA modification commonly found on rRNA and snRNA, and at the mRNA 5'-cap, but has more recently been found internally on mRNA. The study of internal Nm modifications on mRNA is in the early stages, but we have reported that this sort of Nm modification can regulate mRNA abundance and translation. Although there are many methods to determine the presence of Nm on rRNA, detecting Nm on specific mRNA transcripts is technically difficult because they are much less abundant than rRNA. Some of these methods rely on the fact that Nm modification of RNA disrupts reverse transcription reactions when performed at low dNTP concentrations. In this chapter, we describe our approach to using quantitative PCR in conjunction with reverse transcription at low dNTPs, which is sensitive enough to detect changes to Nm modification of mRNA.

Entities:  

Keywords:  2′-O-methylation; Low dNTP; RNA modifications; Reverse transcription; qPCR

Year:  2021        PMID: 34085245     DOI: 10.1007/978-1-0716-1374-0_11

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  12 in total

1.  Global Epitranscriptomics Profiling of RNA Post-Transcriptional Modifications as an Effective Tool for Investigating the Epitranscriptomics of Stress Response.

Authors:  Rebecca E Rose; Manuel A Pazos; M Joan Curcio; Daniele Fabris
Journal:  Mol Cell Proteomics       Date:  2016-01-05       Impact factor: 5.911

2.  Methylated, blocked 5 termini in HeLa cell mRNA.

Authors:  Y Furuichi; M Morgan; A J Shatkin; W Jelinek; M Salditt-Georgieff; J E Darnell
Journal:  Proc Natl Acad Sci U S A       Date:  1975-05       Impact factor: 11.205

3.  Methylated nucleotides block 5' terminus of HeLa cell messenger RNA.

Authors:  C M Wei; A Gershowitz; B Moss
Journal:  Cell       Date:  1975-04       Impact factor: 41.582

4.  A new method for detecting sites of 2'-O-methylation in RNA molecules.

Authors:  Y T Yu; M D Shu; J A Steitz
Journal:  RNA       Date:  1997-03       Impact factor: 4.942

5.  Nm-seq maps 2'-O-methylation sites in human mRNA with base precision.

Authors:  Qing Dai; Sharon Moshitch-Moshkovitz; Dali Han; Nitzan Kol; Ninette Amariglio; Gideon Rechavi; Dan Dominissini; Chuan He
Journal:  Nat Methods       Date:  2017-05-15       Impact factor: 28.547

6.  Mapping 2'-O-methyl groups in ribosomal RNA.

Authors:  B E Maden
Journal:  Methods       Date:  2001-11       Impact factor: 3.608

7.  Illumina-based RiboMethSeq approach for mapping of 2'-O-Me residues in RNA.

Authors:  Virginie Marchand; Florence Blanloeil-Oillo; Mark Helm; Yuri Motorin
Journal:  Nucleic Acids Res       Date:  2016-06-14       Impact factor: 16.971

8.  High-throughput and site-specific identification of 2'-O-methylation sites using ribose oxidation sequencing (RibOxi-seq).

Authors:  Yinzhou Zhu; Stephan P Pirnie; Gordon G Carmichael
Journal:  RNA       Date:  2017-05-11       Impact factor: 4.942

9.  Nucleotide modifications within bacterial messenger RNAs regulate their translation and are able to rewire the genetic code.

Authors:  Thomas Philipp Hoernes; Nina Clementi; Klaus Faserl; Heidelinde Glasner; Kathrin Breuker; Herbert Lindner; Alexander Hüttenhofer; Matthias David Erlacher
Journal:  Nucleic Acids Res       Date:  2015-11-17       Impact factor: 16.971

10.  2'-O-methylation in mRNA disrupts tRNA decoding during translation elongation.

Authors:  Junhong Choi; Gabriele Indrisiunaite; Hasan DeMirci; Ka-Weng Ieong; Jinfan Wang; Alexey Petrov; Arjun Prabhakar; Gideon Rechavi; Dan Dominissini; Chuan He; Måns Ehrenberg; Joseph D Puglisi
Journal:  Nat Struct Mol Biol       Date:  2018-02-19       Impact factor: 15.369

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