Sequencing RNA by a combination of exonuclease digestion and uridine specific chemical cleavage using MALDI-TOF
Author(s) -
D. A. Tolson,
Neville Nicholson
Publication year - 1998
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/26.2.446
Subject(s) - exonuclease , biology , exonuclease iii , rna , oligonucleotide , restriction enzyme , endonuclease , duplex (building) , dna , microbiology and biotechnology , genetics , computational biology , gene , escherichia coli , polymerase
The determination of DNA sequences by partial exonuclease digestion followed by Matrix-Assisted Laser Desorption Time of Flight Mass Spectrometry (MALDI-TOF) is a well established method. When the same procedure is applied to RNA, difficulties arise due to the small (1 Da) mass difference between the nucleotides U and C, which makes unambiguous assignment difficult using a MALDI-TOF instrument. Here we report our experiences with sequence specific endonucleases and chemical methods followed by MALDI-TOF to resolve these sequence ambiguities. We have found chemical methods superior to endonucleases both in terms of correct specificity and extent of sequence coverage. This methodology can be used in combination with exonuclease digestion to rapidly assign RNA sequences.
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