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TransReg SIGNED

Transgenerational epigenetic inheritance of cardiac regenerative capacity in the zebrafish

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 TransReg project word cloud

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

exposed    origins    epigenetic    causing    capacity    fish    offspring    starvation    reveal    models    gene    subpopulations    organ    transmitted    effect    gametes    grandchildren    functional    cardiovascular    sperm    humans    generation    hepatic    environment    regeneration    liver    revealed    sequence    ultimately    toxicants    unravel    zebrafish    metabolism    injured    influence    hearts    altered    infarction    reconstruction    rats    ventricular    regenerative    constitute    underlying    pivotal    plasticity    adverse    elucidated    histone    cell    progenitors    remodeling    fibrosis    shift    parents    basis    disease    similarly    modifications    leads    equally    animals    elicits    network    dna    parental    describe    transgenerational    transfer    time    regenerate    regulatory    suggested    coding    starting    rnas    experiences    regenerated    grandparents    genetic    tei    methylation    myocardial    inheritance    heart    independent    priming    play    injury    degree    model    mechanism    cardiac    describes    cardiomyocyte    while    suffered    paradigm    injuries    analyze    first   

Project "TransReg" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITAET BERN 

Organization address
address: HOCHSCHULSTRASSE 6
city: BERN
postcode: 3012
website: http://www.unibe.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 1˙999˙125 €
 EC max contribution 1˙999˙125 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-COG
 Funding Scheme ERC-COG
 Starting year 2019
 Duration (year-month-day) from 2019-08-01   to  2024-07-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITAET BERN CH (BERN) coordinator 1˙672˙875.00
2    CENTRO NACIONAL DE INVESTIGACIONESCARDIOVASCULARES CARLOS III (F.S.P.) ES (MADRID) participant 326˙250.00

Map

 Project objective

While myocardial infarction leads to adverse ventricular remodeling ultimately causing heart failure in humans, some animals, including zebrafish can regenerate the injured heart. We recently revealed a high degree of plasticity in cardiomyocyte subpopulations involved in the reconstruction of the injured heart. The gene regulatory network involved in heart regeneration is starting to be elucidated and epigenetic remodeling has been suggested to play a pivotal role during this process. Similarly it is known that the environment can influence the regenerative capacity but whether such an effect can be transmitted from one generation to the next has not been addressed. This mechanism is called transgenerational epigenetic inheritance (TEI) and describes the transfer of experiences from parents to their offspring through the gametes, independent on changes in DNA sequence. TEI has also been described in humans: starvation suffered by grandparents affects the metabolism of grandchildren. TEI is also relevant to organ injury: in rats, offspring from parents exposed to liver toxicants revealed reduced hepatic fibrosis in response to the same injury. Changes in DNA methylation, histone modifications and non-coding RNAs have been associated to TEI. We aim to describe for the first time epigenetic inheritance of organ regeneration and unravel its underlying mechanism using the zebrafish model. We will assess whether cardiac injury elicits epigenetic modifications in sperm and determine if offspring from injured parental fish reveal altered heart regeneration. Genetic models will be developed for functional assessment of identified modifications. We will also further analyze cell plasticity during heart regeneration and address whether hearts regenerated from different progenitors respond equally well to further injuries. Our expected findings will constitute a paradigm shift on the origins of cardiovascular disease and define epigenetic priming as a basis for regeneration.

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

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