Opendata, web and dolomites

dynamicmodifications SIGNED

Complexity and dynamics of nucleic acids modifications in vivo

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 dynamicmodifications project word cloud

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

starts    insights    hundreds    lc    capacity    rna    combination    dynamics    organism    containing    characterised    efforts    regeneration    layer    challenged    germ    give    models    nuclear    genomics    fertilised    wound    additionally    inherited    transdifferentiation    subsequent    events    mouse    development    character    teams    understand    chromatin    dictates    specialised    types    naturally    cellular    toti    totipotent    transfer    modifications    sensitive    genome    ie    acquired    lower    takes    primordial    intense    generate    unidirectional    laid    epigenetic    stable    underlie    memory    progressively    onset    fate    fundamental    components    cell    enigmatic    pluripotent    periods    stem    de    dna    implicated    advantage    divisions    progress    interplay    zygote    decisions    differentiation    ultra    cells    organisms    developmental    lost    erasure    embryonic    molecular    interactions    series    reprogramming    paradigm    despite    methylation    healing    ms    mechanisms   

Project "dynamicmodifications" data sheet

The following table provides information about the project.

Coordinator
IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE 

Organization address
address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ
website: http://www.imperial.ac.uk/

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 United Kingdom [UK]
 Project website https://lms.mrc.ac.uk/research-group/reprogramming-and-chromatin/
 Total cost 2˙000˙000 €
 EC max contribution 2˙000˙000 € (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 2015-08-01   to  2020-07-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE UK (LONDON) coordinator 2˙000˙000.00

Map

 Project objective

Development of any organism starts with a totipotent cell (zygote). Through series of cell divisions and differentiation processes this cell will eventually give rise to the whole organism containing hundreds of specialised cell. While the cells at the onset of development have the capacity to generate all cell types (ie are toti-or pluripotent), this developmental capacity is progressively lost as the cells undertake cell fate decisions. At the molecular level, the memory of these events is laid down in a complex layer of epigenetic modifications at both the DNA and the chromatin level. Unidirectional character of the developmental progress dictates that the key acquired epigenetic modifications are stable and inherited through subsequent cell divisions. This paradigm is, however, challenged during cellular reprogramming that requires de-differentiation (nuclear transfer, induced pluripotent stem cells, wound healing and regeneration in lower organisms) or a change in cell fate (transdifferentiation). Despite intense efforts of numerous research teams, the molecular mechanisms of these processes remain enigmatic. In order to understand cellular reprogramming at the molecular level, this proposal takes advantage of epigenetic reprogramming processes that occur naturally during mouse development. By using mouse fertilised zygote and mouse developing primordial germ cells we will investigate novel molecular components implicated in the genome-wide erasure of DNA methylation. Additionally, by using a unique combination of the developmental models with the state of the art ultra-sensitive LC/MS and genomics approaches we propose to investigate the dynamics and the interplay between DNA and RNA modifications during these key periods of embryonic development characterised by genome-wide epigenetic changes . Our work will thus provide new fundamental insights into a complex dynamics and interactions between epigenetic modifications that underlie epigenetic reprogramming

 Publications

year authors and title journal last update
List of publications.
2018 Harry G. Leitch, Petra Hajkova
Eggs sense high-fat diet
published pages: , ISSN: 1061-4036, DOI: 10.1038/s41588-018-0068-1
Nature Genetics 2019-06-07
2017 Laure Ferry, Alexandra Fournier, Takeshi Tsusaka, Guillaume Adelmant, Tadahiro Shimazu, Shohei Matano, Olivier Kirsh, Rachel Amouroux, Naoshi Dohmae, Takehiro Suzuki, Guillaume J. Filion, Wen Deng, Maud de Dieuleveult, Lauriane Fritsch, Srikanth Kudithipudi, Albert Jeltsch, Heinrich Leonhardt, Petra Hajkova, Jarrod A. Marto, Kyohei Arita, Yoichi Shinkai, Pierre-Antoine Defossez
Methylation of DNA Ligase 1 by G9a/GLP Recruits UHRF1 to Replicating DNA and Regulates DNA Methylation
published pages: 550-565.e5, ISSN: 1097-2765, DOI: 10.1016/j.molcel.2017.07.012
Molecular Cell 67/4 2019-06-07
2018 Silvana Rošić, Rachel Amouroux, Cristina E. Requena, Ana Gomes, Max Emperle, Toni Beltran, Jayant K. Rane, Sarah Linnett, Murray E. Selkirk, Philipp H. Schiffer, Allison J. Bancroft, Richard K. Grencis, Albert Jeltsch, Petra Hajkova, Peter Sarkies
Evolutionary analysis indicates that DNA alkylation damage is a byproduct of cytosine DNA methyltransferase activity
published pages: , ISSN: 1061-4036, DOI: 10.1038/s41588-018-0061-8
Nature Genetics 2019-06-07
2017 Annalisa Izzo, Céline Ziegler-Birling, Peter W.S. Hill, Lydia Brondani, Petra Hajkova, Maria-Elena Torres-Padilla, Robert Schneider
Dynamic changes in H1 subtype composition during epigenetic reprogramming
published pages: 3017-3028, ISSN: 0021-9525, DOI: 10.1083/jcb.201611012
The Journal of Cell Biology 216/10 2019-06-07
2016 Rachel Amouroux, Buhe Nashun, Kenjiro Shirane, Shoma Nakagawa, Peter W. S. Hill, Zelpha D’Souza, Manabu Nakayama, Masashi Matsuda, Aleksandra Turp, Elodie Ndjetehe, Vesela Encheva, Nobuaki R. Kudo, Haruhiko Koseki, Hiroyuki Sasaki, Petra Hajkova
De novo DNA methylation drives 5hmC accumulation in mouse zygotes
published pages: 225-233, ISSN: 1465-7392, DOI: 10.1038/ncb3296
Nature Cell Biology 18/2 2019-06-07
2018 Peter W. S. Hill, Harry G. Leitch, Cristina E. Requena, Zhiyi Sun, Rachel Amouroux, Monica Roman-Trufero, Malgorzata Borkowska, Jolyon Terragni, Romualdas Vaisvila, Sarah Linnett, Hakan Bagci, Gopuraja Dharmalingham, Vanja Haberle, Boris Lenhard, Yu Zheng, Sriharsa Pradhan, Petra Hajkova
Epigenetic reprogramming enables the transition from primordial germ cell to gonocyte
published pages: 392-396, ISSN: 0028-0836, DOI: 10.1038/nature25964
Nature 555/7696 2019-06-07
2016 Harry G. Leitch, M. Azim Surani, Petra Hajkova
DNA (De)Methylation: The Passive Route to Naïvety?
published pages: 592-595, ISSN: 0168-9525, DOI: 10.1016/j.tig.2016.08.005
Trends in Genetics 32/10 2019-06-07

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

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

KineTic (2020)

New Reagents for Quantifying the Routing and Kinetics of T-cell Activation

Read More  

CARBYNE (2020)

New carbon reactivity rules for molecular editing

Read More  

TechChange (2019)

Technological Change: New Sources, Consequences, and Impact Mitigation

Read More