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.

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

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  

CELPRED (2020)

Circuit elements of the cortical circuit for predictive processing

Read More  

CellProbe (2019)

CellProbe: Microfluidic probe for simultaneous tagging and extraction of single cells

Read More