0000000001309841

AUTHOR

Antonia Ochel

showing 4 related works from this author

Variable presence of 5-methylcytosine in commercial RNA and DNA

2015

Nucleoside methylations and other nucleic acid modifications have recently encountered a surge in interest, prompted, among other things, by the detection of methylation and active demethylation of DNA and mRNA by similar mechanisms. In DNA, deoxycytidine methylation by Dnmt enzymes generates 5-methyldeoxycytidine,1 an important epigenetic mark that typically causes inactivation of transcription of the methylated promoter region. Recent exciting developments have shown that these marks are not concrete-cast, but can be actively removed by the oxidative action of TET enzymes,2 which generate, through a series of 2-electron oxidations, first hydroxymethylcytidine (hm5C), then formyldeoxycytid…

Bisulfite sequencingSaccharomyces cerevisiaeBiologyMass Spectrometrychemistry.chemical_compoundTranscription (biology)Escherichia coliMethylated DNA immunoprecipitationmodified nucleosideMolecular BiologyOligonucleotideRNADNACell BiologyRNA modificationMolecular biology5-MethylcytosinechemistryBiochemistry5-MethylcytosineNucleic acidRNADNA modificationDNAResearch PapermethylcytosineChromatography LiquidRNA Biology
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Structure-Function Relationship of Substituted Bromomethylcoumarins in Nucleoside Specificity of RNA Alkylation

2013

Selective alkylation of RNA nucleotides is an important field of RNA biochemistry, e.g. in applications of fluorescent labeling or in structural probing experiments, yet detailed structure-function studies of labeling agents are rare. Here, bromomethylcoumarins as reactive compounds for fluorescent labeling of RNA are developed as an attractive scaffold on which electronic properties can be modulated by varying the substituents. Six different 4-bromomethyl-coumarins of various substitution patterns were tested for nucleotide specificity of RNA alkylation using tRNA from Escherichia coli as substrate. Using semi-quantitative LC-MS/MS analysis, reactions at mildly acidic and slightly alkaline…

AlkylationStaining and LabelingScienceQRNucleosidesRNA BacterialStructure-Activity RelationshipRNA TransferCoumarinsEscherichia coliMedicine500 Natural sciences and mathematics500 NaturwissenschaftenResearch ArticleFluorescent DyesPLoS ONE
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Absolute and relative quantification of RNA modifications via biosynthetic isotopomers

2014

In the resurging field of RNA modifications, quantification is a bottleneck blocking many exciting avenues. With currently over 150 known nucleoside alterations, detection and quantification methods must encompass multiple modifications for a comprehensive profile. LC-MS/MS approaches offer a perspective for comprehensive parallel quantification of all the various modifications found in total RNA of a given organism. By feeding (13)C-glucose as sole carbon source, we have generated a stable isotope-labeled internal standard (SIL-IS) for bacterial RNA, which facilitates relative comparison of all modifications. While conventional SIL-IS approaches require the chemical synthesis of single mod…

Carbon IsotopesTandem Mass SpectrometryEscherichia coli500 Natural sciences and mathematicsMethods OnlineRNANucleosides500 NaturwissenschaftenReference Standards13PseudouridineChromatography LiquidNucleic Acids Research
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Variable presence of 5-methylcytosine in commercial RNA and DNA

2015

5-methylcytosine (m5C, mC) is a naturally occurring nucleoside modification in both RNA and DNA. Its presence in DNA is a widely accepted epigenetic mark for transcription inactivation. In RNA, its appearance in different coding as well as non-coding RNA implies multiple functions, with regulation of gene expression as a common denominator. Here we report on the serendipitous discovery of m5C in synthetic oligonucleotides, which prompted a systematic quantification in synthetic DNA and RNA of academic as well as of commercial origin. For both types of oligonucleotides, m5C was identified by comparison of fragmentation pattern and retention time with authentic standards by highly sensitive L…

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