5‐Formylcytosine Could Be a Semipermanent Base in Specific Genome Sites. Issue 39 (25th August 2016)

• Record Type: Journal Article
• Authors: Su, Meng; Kirchner, Angie; Stazzoni, Samuele; Müller, Markus; Wagner, Mirko; Schröder, Arne; Carell, Thomas
• Is Part Of: Angewandte Chemie international edition. Volume 55:Issue 39(2016)
• Page Start: 11797
• Page End: 11800
• Publication Date: 2016-08-25
• Subjects: 5-formylcytosine -- click chemistry -- droplet digital PCR -- epigenetic bases -- genomic DNA; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.201605994
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: 5‐Formyl‐2′‐deoxycytosine (fdC) is a recently discovered epigenetic base in the genome of stem cells, with yet unknown functions. Sequencing data show that the base is enriched in CpG islands of promoters and hence likely involved in the regulation of transcription during cellular differentiation. fdC is known to be recognized and excised by the enzyme thymine‐DNA‐glycosylase (Tdg). As such, fdC is believed to function as an intermediate during active demethylation. In order to understand the function of the new epigenetic base fdC, it is important to analyze its formation and removal at defined genomic sites. Here, we report a new method that combines sequence‐specific chemical derivatization of fdC with droplet digital PCR that enables such analysis. We show initial data, indicating that the repair protein Tdg removes only 50 % of the fdCs at a given genomic site, arguing that fdC is a semipermanent base. Abstract : Big hug for fdC : A method for the site‐specific quantification of the epigenetic base 5‐formylcytosine (fdC) was developed. Applied on the genome of an mESC population, the assay showed that the repair enzyme Tdg removes only half of the fdC bases at a given genomic site.