Objectif Cells have a broad functional and morphological diversity due to differential gene expression. Research in epigenetics combines the study of inheritable, phenotypical changes in the gene expression pattern of a specific cell type that are not caused by a transformed nucleotide sequence of the genetic code itself. Epigenetic marks are represented by a variety of molecular mechanisms including DNA methylation. Alterations of DNA methylation play a crucial role in the onset of diseases like cancer. Many DNA methylation-based biomarkers have been evaluated and the analysis of epigenetic alterations is a promising tool for disease diagnostics, prognostics, and prediction of drug response. In future, this will allow to adapt therapies to a person, which will increase the chance for successful treatments, minimizing side-effects of chemotherapy and administration of ineffective drugs and thus, prevent the onset of follow-up problems that are associated with these events. Thus, cost-effective but robust means that allow the analysis of DNA methylation-based biomarkers are of urgent need. Several methods for analysis of these biomarkers are employed. However, those that have the required resolution are laborious, time-consuming, and error-prone and thus, prevent broad applications of DNA methylation profiling in clinical diagnostics. The aim of this project is to overcome the barriers that prohibit using DNA methylation profiling in broad clinical applications for diagnostics, prognostics, and prediction of drug response. The objectives will be reached by a multidisciplinary systemic approach harnessing the power of organic synthesis (i.e. new synthetic modified nucleotides), biochemical and structural enzyme studies, and directed evolution of DNA polymerases tailored for new replication systems for epigenetics. The evolved replication systems will be superior to known techniques by superseding the bottle necks of current approaches paving the way for broad applications. Champ scientifique natural sciencesbiological sciencesgeneticsDNAmedical and health sciencesclinical medicineoncologynatural sciencesbiological sciencesgeneticsnucleotidesnatural sciencesbiological sciencesbiochemistrybiomoleculesproteinsenzymesnatural sciencesbiological sciencesgeneticsepigenetics Programme(s) FP7-IDEAS-ERC - Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) Thème(s) ERC-AG-LS9 - ERC Advanced Grant - Applied life sciences and biotechnology Appel à propositions ERC-2013-ADG Voir d’autres projets de cet appel Régime de financement ERC-AG - ERC Advanced Grant Institution d’accueil UNIVERSITAT KONSTANZ Contribution de l’UE € 2 483 966,40 Adresse UNIVERSITATSSTRASSE 10 78464 Konstanz Allemagne Voir sur la carte Région Baden-Württemberg Freiburg Konstanz Type d’activité Higher or Secondary Education Establishments Chercheur principal Andreas Marx (Prof.) Contact administratif Claudia Knueppel (Ms.) Liens Contacter l’organisation Opens in new window Site web Opens in new window Coût total Aucune donnée Bénéficiaires (1) Trier par ordre alphabétique Trier par contribution de l’UE Tout développer Tout réduire UNIVERSITAT KONSTANZ Allemagne Contribution de l’UE € 2 483 966,40 Adresse UNIVERSITATSSTRASSE 10 78464 Konstanz Voir sur la carte Région Baden-Württemberg Freiburg Konstanz Type d’activité Higher or Secondary Education Establishments Chercheur principal Andreas Marx (Prof.) Contact administratif Claudia Knueppel (Ms.) Liens Contacter l’organisation Opens in new window Site web Opens in new window Coût total Aucune donnée