Explore the words cloud of the Epiherigans project. It provides you a very rough idea of what is the project "Epiherigans" about.
The following table provides information about the project.
Coordinator |
FRIEDRICH MIESCHER INSTITUTE FOR BIOMEDICAL RESEARCH FONDATION
Organization address contact info |
Coordinator Country | Switzerland [CH] |
Total cost | 2˙500˙000 € |
EC max contribution | 2˙500˙000 € (100%) |
Programme |
1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC)) |
Code Call | ERC-2016-ADG |
Funding Scheme | ERC-ADG |
Starting year | 2017 |
Duration (year-month-day) | from 2017-06-01 to 2022-05-31 |
Take a look of project's partnership.
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1 | FRIEDRICH MIESCHER INSTITUTE FOR BIOMEDICAL RESEARCH FONDATION | CH (BASEL) | coordinator | 2˙500˙000.00 |
Epigenetic inheritance is the transmission of information, generally in the form of DNA methylation or post-translational modifications on histones that regulate the availability of underlying genetic information for transcription. RNA itself feeds back to contribute to histone modification. Sequence accessibility is both a matter of folding the chromatin fibre to alter access to recognition motifs, and the local concentration of factors needed for efficient transcriptional initiation, elongation, termination or mRNA stability. In heterochromatin we find a subset of regulatory factors in carefully balanced concentrations that are maintained in part by the segregation of active and inactive domains. Histone H3 K9 methylation is key to this compartmentation. C. elegans provides an ideal system in which to study chromatin-based gene repression. We have demonstrated that histone H3 K9 methylation is the essential signal for the sequestration of heterochromatin at the nuclear envelope in C. elegans. The recognition of H3K9me1/2/3 by an inner nuclear envelope-bound chromodomain protein, CEC-4, actively sequesters heterochromatin in embryos, and contributes redundantly in adult tissues. Epiherigans has the ambitious goal to determine definitively what targets H3K9 methylation, and identify its physiological roles. We will examine how this mark contributes to the epigenetic recognition of repeat vs non-repeat sequence, and mediates a stress-induced response to oxidative damage. We will examine the link between these and the spatial clustering of heterochromatic domains. Epiherigans will develop an integrated approach to identify in vivo the factors that distinguish repeats from non-repeats, self from non-self within genomes and will examine how H3K9me contributes to a persistent ROS or DNA damage stress response. It represents a crucial step towards understanding of how our genomes use heterochromatin to modulate, stabilize and transmit chromatin organization.
year | authors and title | journal | last update |
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2019 |
Jan Padeken, Peter Zeller, Benjamin Towbin, Iskra Katic, Veronique Kalck, Stephen P. Methot, Susan M. Gasser Synergistic lethality between BRCA1 and H3K9me2 loss reflects satellite derepression published pages: 436-451, ISSN: 0890-9369, DOI: 10.1101/gad.322495.118 |
Genes & Development 33/7-8 | 2020-02-05 |
2019 |
Colin E. Delaney, Stephen P. Methot, Micol Guidi, Iskra Katic, Susan M. Gasser, Jan Padeken Heterochromatic foci and transcriptional repression by an unstructured MET-2/SETDB1 co-factor LIN-65 published pages: 820-838, ISSN: 0021-9525, DOI: 10.1083/jcb.201811038 |
The Journal of Cell Biology 218/3 | 2020-02-05 |
2019 |
Daphne S. Cabianca, Celia Muñoz-Jiménez, Véronique Kalck, Dimos Gaidatzis, Jan Padeken, Andrew Seeber, Peter Askjaer, Susan M. Gasser Active chromatin marks drive spatial sequestration of heterochromatin in C. elegans nuclei published pages: 734-739, ISSN: 0028-0836, DOI: 10.1038/s41586-019-1243-y |
Nature 569/7758 | 2020-02-05 |
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The information about "EPIHERIGANS" are provided by the European Opendata Portal: CORDIS opendata.