| Literature DB >> 28371147 |
Sarah Schiffers1, Charlotte Ebert1, René Rahimoff1, Olesea Kosmatchev1, Jessica Steinbacher1, Alexandra-Viola Bohne2, Fabio Spada1, Stylianos Michalakis3, Jörg Nickelsen2, Markus Müller1, Thomas Carell1.
Abstract
Until recently, it was believed that the genomes of higher organisms contain, in addition to the four canonical DNA bases, only 5-methyl-dC (m5 dC) as a modified base to control epigenetic processes. In recent years, this view has changed dramatically with the discovery of 5-hydroxymethyl-dC (hmdC), 5-formyl-dC (fdC), and 5-carboxy-dC (cadC) in DNA from stem cells and brain tissue. N6 -methyldeoxyadenosine (m6 dA) is the most recent base reported to be present in the genome of various eukaryotic organisms. This base, together with N4 -methyldeoxycytidine (m4 dC), was first reported to be a component of bacterial genomes. In this work, we investigated the levels and distribution of these potentially epigenetically relevant DNA bases by using a novel ultrasensitive UHPLC-MS method. We further report quantitative data for m5 dC, hmdC, fdC, and cadC, but we were unable to detect either m4 dC or m6 dA in DNA isolated from mouse embryonic stem cells or brain and liver tissue, which calls into question their epigenetic relevance.Entities:
Keywords: DNA; epigenetics; mass spectrometry; methyldeoxyadenosine; methyldeoxycytidine
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Year: 2017 PMID: 28371147 DOI: 10.1002/anie.201700424
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336