Opendata, web and dolomites

Epiherigans SIGNED

Writing, reading and managing stress with H3K9me

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 Epiherigans project word cloud

Explore the words cloud of the Epiherigans project. It provides you a very rough idea of what is the project "Epiherigans" about.

actively    active    persistent    local    stability    h3k9    methylation    dna    chromatin    sequence    redundantly    k9    subset    post    examine    genetic    segregation    damage    inheritance    regulate    adult    epigenetic    mediates    embryos    mrna    oxidative    link    modifications    histones    back    transcriptional    signal    h3    itself    motifs    generally    roles    inner    repression    provides    cec    efficient    heterochromatin    chromodomain    sequesters    stress    histone    modulate    vs    ideal    balanced    carefully    physiological    concentration    maintained    tissues    accessibility    heterochromatic    mark    feeds    transcription    epiherigans    genomes    distinguish    fibre    transmit    h3k9me    spatial    modification    gene    elongation    compartmentation    repeat    form    protein    transmission    self    definitively    envelope    domains    termination    elegans    nuclear    repeats    translational    alter    organization    stabilize    h3k9me1    bound    concentrations    rna    regulatory    contributes    initiation    recognition    inactive    ros    folding    clustering    sequestration    demonstrated    underlying    vivo   

Project "Epiherigans" data sheet

The following table provides information about the project.

Coordinator
FRIEDRICH MIESCHER INSTITUTE FOR BIOMEDICAL RESEARCH FONDATION 

Organization address
address: MAULBEERSTRASSE 66
city: BASEL
postcode: 4058
website: www.fmi.ch

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 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

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FRIEDRICH MIESCHER INSTITUTE FOR BIOMEDICAL RESEARCH FONDATION CH (BASEL) coordinator 2˙500˙000.00

Map

 Project objective

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.

 Publications

year authors and title journal last update
List of publications.
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

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "EPIHERIGANS" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

The information about "EPIHERIGANS" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.1.)

ERC VP CSA (2018)

Support to the Vice-Presidents of the ERC Scientific Council 2018

Read More  

AST (2019)

Automatic System Testing

Read More  

RTMFRM (2019)

Room Temperature Magnetic Resonance Force Microscopy

Read More