A mass spectrometry-based method for direct determination of pseudouridine in RNA
Author(s) -
Yoshio Yamauchi,
Yuko Nobe,
Keiichi Izumikawa,
Daisuke Higo,
Yoko Yamagishi,
Nobuhiro Takahashi,
Hiroshi Nakayama,
Toshiaki Isobe,
Masato Taoka
Publication year - 2015
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkv1462
Subject(s) - pseudouridine , rna , biology , nucleoside , mass spectrometry , nucleobase , nucleotide , computational biology , fragmentation (computing) , oligonucleotide , dna , biochemistry , transfer rna , gene , chemistry , chromatography , ecology
Pseudouridine (5-ribosyluracil, Ψ) is the only 'mass-silent' nucleoside produced by post-transcriptional RNA modification. We describe here a novel mass spectrometry (MS)-based method for direct determination of Ψ in RNA. The method assigns a Ψ-containing nucleolytic RNA fragment by an accurate measurement of a signature doubly dehydrated nucleoside anion ([C9H7N2O4](1-), m/z 207.04) produced by collision-induced dissociation MS, and it determines the Ψ-containing nucleotide sequence by pseudo-MS(3), i.e. in-source fragmentation followed by MS(2). By applying this method, we identified all of the known Ψs in the canonical human spliceosomal snRNAs and, unexpectedly, found two previously unknown Ψs in the U5 and U6 snRNAs. Because the method allows direct determination of Ψ in a subpicomole quantity of RNA, it will serve as a useful tool for the structure/function studies of a wide variety of non-coding RNAs.
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