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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.

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

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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