#	Pagina
attuale pagina	/open-h2020/projects/194512/index.html
-1	/open-h2020/projects/207814/index.html
-2	/open-h2020/projects/221639/index.html
-3	/open-h2020/projects/209536/index.html
-4	/open-h2020/projects/214557/index.html
-5	/open-h2020/projects/222274/index.html
-6	/open-h2020/projects/214466/index.html
-7	/open-h2020/projects/221414/index.html
-8	/open-h2020/projects/200532/index.html
-9	/open-h2020/projects/221202/index.html
-10	/open-h2020/projects/207602/index.html

Opendata, web and dolomites

NChIP SIGNED

Chromatin dynamics during DNA replication

Total Cost €

EC-Contrib. €

Partnership

Views

Outcomes and
results

NChIP project word cloud

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

400bp daughter theory newly fold dynamics binding transcriptional perturbations site prerequisite epigenetic tetramers throughput dna original footprint potentially lagging nucleosomes h3 regulators thought diluted disease renewal se demonstrated components later domains genomic inherited establishment protein environmental blocs activation unmarked gene reassembly inheritance kinetics heritable survive facts phenomena synthesized genome distribute few histone encoded maintenance posttranslational cancer spread proteins accepted strand histones strands chromatin differentiation integrity shown h4 driver predispositions maternal previously re bulk 1kb programs measuring smaller implying assembly effect stay differences split equally cellular replication fundamental cerevisiae influence locus movements positioning nucleosome marks majority

Project "NChIP" data sheet

The following table provides information about the project.

Coordinator	CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS Organization address address: RUE MICHEL ANGE 3 city: PARIS postcode: 75794 website: www.cnrs.fr 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	France [FR]
Total cost	1˙984˙677 €
EC max contribution	1˙984˙677 € (100%)
Programme	1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
Code Call	ERC-2014-CoG
Funding Scheme	ERC-COG
Starting year	2015
Duration (year-month-day)	from 2015-06-01 to 2020-05-31

Partnership

Take a look of project's partnership.

#	participants	country	role	EC contrib. [€]
1	CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS Organization address address: RUE MICHEL ANGE 3 city: PARIS postcode: 75794 website: www.cnrs.fr contact info title: n.a. name: n.a. surname: n.a. function: n.a. email: n.a. telephone: n.a. fax: n.a.	FR (PARIS)	coordinator	1˙984˙677.00

Map

Project objective

Chromatin assembly is a fundamental cellular process necessary for the maintenance of genome integrity and transcriptional programs. Understanding the effect of DNA replication on histone protein dynamics is also a prerequisite for understanding the role of chromatin in epigenetic inheritance. Epigenetic phenomena are thought to influence cellular differentiation and cancer formation, as well as the impact of environmental factors on early development and later predispositions to disease. While epigenetic inheritance of chromatin components is, in theory, accepted as the driver of such phenomena, chromatin state inheritance per se has only been demonstrated for a few specific cases. Not much is known about histone “inheritance” beyond the facts that bulk maternal histones distribute equally among the daughter strands and are diluted two-fold after replication with newly synthesized “unmarked” histones, and that the majority of H3/H4 tetramers do not split before reassembly. We have shown previously that maternal nucleosomes stay on average within 400bp of their original binding site, implying that any potentially heritable chromatin encoded information, has to be inherited in ~1kb blocs, as smaller nucleosome domains would rapidly be diluted by new nucleosomes. I propose to develop high throughput systems for directly measuring movements of histones and chromatin regulators during genomic replication in S.cerevisiae to determine, how chromatin states survive the perturbations associated with replication. We will determine locus specific differences in the spread of maternal nucleosomes after replication, the effects of leading and lagging strand replication on nucleosome positioning and maternal nucleosome distribution, the renewal dynamics of posttranslational histone marks and chromatin binding proteins, and the kinetics of chromatin footprint re-establishment and gene (re)activation.

Publications

List of publications.
year	authors and title	journal	last update
2019	Rahima Ziane, Alain Camasses, Marta Radman-Livaja Mechanics of DNA Replication and Transcription Guide the Asymmetric Distribution of RNAPol2 and New Nucleosomes on Replicated Daughter Genomes published pages: , ISSN: , DOI: 10.1101/553669	biorxiv	2020-02-05
2019	Hrvoje Galic, Pauline Vasseur,Marta Radman-Livaja The budding yeast heterochromatic SIR complex resets upon exit from stationary phase published pages: , ISSN: , DOI: 10.1101/603613	biorxiv	2020-02-05
2016	Pauline Vasseur, Saphia Tonazzini, Rahima Ziane, Alain Camasses, OliverÂ J. Rando, Marta Radman-Livaja Dynamics of Nucleosome Positioning Maturation following Genomic Replication published pages: 2651-2665, ISSN: 2211-1247, DOI: 10.1016/j.celrep.2016.07.083	Cell Reports 16/10	2019-06-06

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "NCHIP" 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 "NCHIP" are provided by the European Opendata Portal: CORDIS opendata.