28 research outputs found
Hairpin Bisulfite Sequencing: Synchronous Methylation Analysis on Complementary DNA Strands of Individual Chromosomes
No full textThe role of Dnmts and Tets in shaping the DNA methylation landscape of mouse embryonic stem cells
No full textDNA methylation is an important epigenetic mark, which is set and maintained by DNA methyltransferases (Dnmts) and removed via passive or active mechanisms involving Ten eleven translocation enzyme (Tet) mediated oxidation. Stable cell type specific methylation patterns can only be achieved if methylation and demethylation events are in balance. Yet, the genome wide regulation of Dnmt and Tet activity is still not fully understood. The present studies use novel hairpin sequencing techniques coupled with oxidative bisul te sequencing, which permits the simultaneous and strand speci c detection of 5- methylcytosine and 5-hydroxymethylcytosine. Application of HMM models then facilitates the estimation of enzyme efficiencies for Dnmts and Tets. Furthermore, spatial modelling of hairpin bisulfite data allows the investigation of how Dnmts interpret preexisting methylation patterns. Taken together, the results of the presented studies show that methylation and hydroxylation are antagonistic, but not mutual exclusive events. In this context, the data shows that Tet efficiency is highest at open and accessible chromatin. Furthermore, the absence of Tets leads to a considerable misregulation of Dnmts, resulting in an increase in both maintenance and de novo methylation efficiency. Lastly, the spatial analysis of methylation patterns reveals that the de novo methyltransferases Dnmt3a and 3b depend in their activity on pre-existing neighbouring CpG methylation.DNA Methylierung is eine epigenetische Modifikation, welche durch DNA Methyltransferasen (Dnmts) gesetzt und beibehalten wird. Entfernt wird DNA Methylierung durch aktive oder passive Mechanismen welche die Oxidation von DNA Methylierung durch Ten- Eleven Translocation Enzyme (Tets) involviert. Stabile, Zelltyp-spezifische Methylierungsmuster können nur erreicht werden, wenn Methylierungs- und Demethylierungsvorgänge im Gleichgewicht sind. Dennoch ist die genomweite Regulation von Dnmts und Tets nicht vollständig geklärt. Die hier gezeigten Studien verwenden neue Hairpin-Sequenzierungs-Verfahren, gekoppelt mit oxidativer Bisulfit-Sequenzierung, was eine simultane und strangspezifische Analyse von 5-Methylcytosin und 5-Hydroxymethylcytosin erlaubt. Die Anwendung von hid- den Markov Modellen erlaubt im Anschluss die Berechnung von Enzymeeffizienzen für Dnmts und Tets. Darüber hinaus erlaubt eine räumliche Modellierung von Methylierungsmustern die Untersuchung, wie Dnmts bereits bestehende Methylierung interpretieren. Die Ergebnisse zeigen, dass Methylierung und Hydroxylierung antagonistische, aber keinesfalls sich ausschließende Ereignisse sind. Dabei zeigen Tets ihre stärkste Aktivität an offenem und zugänglichem Chromatin. Zudem führt der Verlust von Tets zu einer deutlichen Missregulation von Dnmts, welche sich durch eine Zunahme der Maintenance und de novo-Methylierungseffizienz äußert. Schließlich zeigt die räumliche Modellierung, dass die de novo-Methyltransferasen bei ihrer Aktivität abhängig von bereits bestehender DNA Methylierung sind
H(O)TA: estimation of DNA methylation and hydroxylation levels and efficiencies from time course data
No full textHistone and DNA methylation control by H3 serine 10/threonine 11 phosphorylation in the mouse zygote
No full textBackground: In the mammalian zygote, epigenetic reprogramming is a tightly controlled process of coordinated alterations of histone and DNA modifications. The parental genomes of the zygote show distinct patterns of histone H3 variants and distinct patterns of DNA and histone modifications. The molecular mechanisms linking histone variant-specific modifications and DNA methylation reprogramming during the first cell cycle remain to be clarified. Results: Here, we show that the degree and distribution of H3K9me2 and of DNA modifications (5mC/5hmC) are influenced by the phosphorylation status of H3S10 and H3T11. The overexpression of the mutated histone variants H3.1 and 3.2 at either serine 10 or threonine 11 causes a decrease in H3K9me2 and 5mC and a concomitant increase in 5hmC in the maternal genome. Bisulphite sequencing results indicate an increase in hemimethylated CpG positions following H3.1T10A overexpression suggesting an impact of H3S10 and H3T11 phosphorylation on DNA methylation maintenance. Conclusions: Our data suggest a crosstalk between the cell-cycle-dependent control of S10 and T11 phosphorylation of histone variants H3.1 and H3.2 and the maintenance of the heterochromatic mark H3K9me2. This histone H3 "phospho-methylation switch" also influences the oxidative control of DNA methylation in the mouse zygote.SCOPUS: ar.jinfo:eu-repo/semantics/publishe
Two are better than one: HPoxBS - hairpin oxidative bisulfite sequencing
No full textThe controlled and stepwise oxidation of 5mC to 5hmC, 5fC and 5caC by Tet enzymes is influencing the chemical and biological properties of cytosine. Besides direct effects on gene regulation, oxidised forms influence the dynamics of demethylation and re-methylation processes. So far, no combined methods exist which allow to precisely determine the strand specific localisation of cytosine modifications along with their CpG symmetric distribution. Here we describe a comprehensive protocol combining conventional hairpin bisulfite with oxidative bisulfite sequencing (HPoxBS) to determine the strand specific distribution of 5mC and 5hmC at base resolution. We apply this method to analyse the contribution of local oxidative effects on DNA demethylation in mouse ES cells. Our method includes the HPoxBS workflow and subsequent data analysis using our developed software tools. Besides a precise estimation and display of strand specific 5mC and 5hmC levels at base resolution we apply the data to predict region specific activities of Dnmt and Tet enzymes. Our experimental and computational workflow provides a precise double strand display of 5mC and 5hmC modifications at single base resolution. Based on our data we predict region specific Tet and Dnmt enzyme efficiencies shaping the distinct locus levels and patterns of 5hmC and 5mC
The Influence of Hydroxylation on Maintaining CpG Methylation Patterns: A Hidden Markov Model Approach
No full textGerman Research Council (DFG) as part of the
Collaborative Research Center "Physical modeling of
non-equilibrium processes in biological systems"
(SFB 1027) and the Cluster of Excellence on
Multimodal Computing and Interaction at Saarland
Universit
Maintenance and de novo methylation are usually cooperating to maintain a stable methylation pattern (inner circle).
No full textThe oxidation of 5mC to 5hmC may interfere with the maintenance machinery causing a (partial) loss of CpG methylation after DNA replication. DNA strands are indicated by lines whereas the CpG are shown as colored circles.</p
Schematic outline of the conversion of Cytosine, 5mC and 5hmC during BS and oxBS treatment and after sequencing: In the bisulfite reaction a cytosine (C) is converted to uracil (U), whereas 5mC and 5hmC remain untouched.
No full textIn the oxidative bisulfite sequencing only 5mC remains untouched and cytosine as well as 5hmC is converted to uracil (U). The conversion errors are illustrated as dashed red arrows and c, d, e, f are the conversion probabilities.</p
