Opendata, web and dolomites

Totipotency SIGNED

Transcriptional and Epigenetic Regulation of Totipotency in Mouse Early Embryos.

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 Totipotency project word cloud

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

technologies    reprogramming    totipotency    candidate    truly    translation    modifiers    eviction    gametes    conditionally    molecular    nuclei    cpg    totipotent    deficient    underlying    zygote    mouse    manner    exquisite    fusion    possibly    modified    coincides    initiate    spermatid    nucleosome    mature    assisted    combined    conditional    significance    utilize    transferring    binding    degradation    mechanisms    inheritance    reproductive    embryos    regulate    tfs    interrogate    human    regulation    developmental    cell    chromatin    epigenetic    immature    organism    computational    sites    barely    med    zga    function    sensitive    later    acquisition    germline    oocytes    parental    live    competence    gives    genomic    nucleosomes    wild    islands    gene    initiation    activation    sperm    contribution    embryonic    dissecting    transcription    transcripts    quantitative    imaging    models    maternally    nascent    erc    fate    mammals    depleting    spermatogenesis    paternal    regulators    histone    genome    biology    zygotic    global    gain    differentiated    landscapes    deficiency    relevance    sophisticated   

Project "Totipotency" 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˙859˙560 €
 EC max contribution 2˙859˙560 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2015-AdG
 Funding Scheme ERC-ADG
 Starting year 2016
 Duration (year-month-day) from 2016-08-01   to  2021-07-31

 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˙859˙560.00

Map

 Project objective

In mammals, fusion of two highly differentiated gametes gives rise to a totipotent zygote capable of developing into a whole organism. It coincides with translation and degradation of maternally provided transcripts, initiation of global transcription called zygotic genome activation (ZGA), and “epigenetic reprogramming” of germline chromatin states into an embryonic state. The molecular mechanisms underlying this exquisite reprogramming of cell fate are barely understood.

This research program has the ambitious goal to identify and characterize in a comprehensive way the transcription factors and chromatin regulators which initiate and regulate ZGA in a parental specific manner in early mouse embryos. We will utilize novel and highly sensitive genomic approaches to measure nascent transcription and determine open and modified chromatin landscapes in oocytes and early embryos, wild-type and conditionally deficient for major epigenetic modifiers. We will apply computational approaches to identify candidate TFs and histone modifiers controlling ZGA. We will use molecular and developmental biology approaches, combined with sensitive quantitative live-imaging, to interrogate the function of TFs and their binding sites for ZGA.

We will further investigate the significance of possible paternal inheritance of nucleosomes at CpG islands for gene regulation during ZGA and later development by depleting nucleosomes from mature sperm by using sophisticated conditional deficiency and gain-of-function mouse models. By transferring nuclei of immature spermatid and mature sperm into oocytes, we will interrogate the relevance of nucleosome eviction during spermatogenesis, as a possibly truly epigenetic reprogramming process, for defining embryonic competence.

ERC funding would represent a crucial contribution to dissecting the molecular mechanisms underlying acquisition of totipotency in mouse embryos and may impact on the use of Assisted Reproductive Technologies in human med

 Publications

year authors and title journal last update
List of publications.
2018 Mark E. Gill, Antoine H. F. M. Peters
Toward human egg-like cells in vitro
published pages: 291-292, ISSN: 0036-8075, DOI: 10.1126/science.aav3479
Science 362/6412 2019-06-03
2019 Maaike Welling, Manuel Alexander Mohr, Aaron Ponti, Lluc Rullan Sabater, Andrea Boni, Yumiko K Kawamura, Prisca Liberali, Antoine HFM Peters, Pawel Pelczar, Periklis Pantazis
Primed Track, high-fidelity lineage tracing in mouse pre-implantation embryos using primed conversion of photoconvertible proteins
published pages: , ISSN: 2050-084X, DOI: 10.7554/elife.44491
eLife 8 2019-06-03

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

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

NanoPD_P (2020)

High throughput multiplexed trace-analyte screening for diagnostics applications

Read More  

NeuroMag (2019)

The Neurological Basis of the Magnetic Sense

Read More  

Photopharm (2020)

Photopharmacology: From Academia toward the Clinic.

Read More