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EVOCELFATE SIGNED

Evolution of cell fate specification modes in spiral cleavage

Total Cost €

0

EC-Contrib. €

0

Partnership

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 EVOCELFATE project word cloud

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

closely    segregation    phyla    spiralian    repeatedly    naturally    interactions    larvae    transcriptional    structures    largely    lineages    ancestral    cleavage    proteomics    spiral    conditionally    chromatin    cleaving    rna    maternal    fate    driving    incorporated    adult    phylogenetic    molecular    supplied    tests    animal    oocytes    phenotypic    biology    fill    techniques    shifted    progenitor    remarkably    modes    stereotypical    cell    fates    posterodorsal    homologous    combine    guided    conditional    experimental    questions    uncover    precocious    evolutionary    clade    specification    autonomous    inputs    developmental    poorly    adultation    autonomously    bioinformatics    seq    differentially    gap    unexplored    embryonic    mechanisms    fundamental    half    specify    context    almost    evolution    comprehensively    embryos    evolve    programs    spiralia    imaging    core    characters    insights    live    species    hypothesis    regulators    variation    repeated    mode    occurs   

Project "EVOCELFATE" data sheet

The following table provides information about the project.

Coordinator
QUEEN MARY UNIVERSITY OF LONDON 

Organization address
address: 327 MILE END ROAD
city: LONDON
postcode: E1 4NS
website: http://www.qmul.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]
 Total cost 1˙500˙000 €
 EC max contribution 1˙500˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-STG
 Funding Scheme ERC-STG
 Starting year 2019
 Duration (year-month-day) from 2019-02-01   to  2024-01-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    QUEEN MARY UNIVERSITY OF LONDON UK (LONDON) coordinator 1˙500˙000.00

Map

 Project objective

Spiral cleavage is a highly stereotypical early embryonic program, and the ancestral, defining feature to Spiralia, a major phylogenetic clade including almost half of the animal phyla. Remarkably, spiral-cleaving embryos specify homologous cell fates (e.g. the progenitor cell of posterodorsal structures) conditionally –via cell interactions– or autonomously –via segregation of maternal inputs. This variation occurs naturally, even between closely related species, and has been related to the precocious formation of adult characters (adultation) in larvae of autonomous spiral-cleaving species. How spiralian lineages repeatedly shifted between these two cell fate specification modes is largely unexplored, because the mechanisms controlling spiral cleavage are still poorly characterized. This project tests the hypothesis that maternal chromatin and transcriptional regulators differentially incorporated in oocytes with autonomous spiral cleavage explain the evolution of this mode of cell fate specification. Through a comparative and phylogenetic-guided approach, we will combine bioinformatics, live imaging, and molecular and experimental techniques to: (i) Comprehensively identify differentially supplied maternal factors among spiral cleaving oocytes with distinct cell fate specification modes using comparative RNA-seq and proteomics; (ii) Uncover the developmental mechanisms driving conditional spiral cleavage, which is the ancestral embryonic mode; and (iii) Investigate how maternal chromatin and transcriptional regulators define early cell fates, and whether these factors account for the repeated evolution of autonomous specification modes. Our results will fill a large gap of knowledge in our understanding of spiral cleavage and its evolution. In a broader context, this project will deliver fundamental insights into two core questions in evolutionary developmental biology: how early embryonic programs evolve, and how they contribute to phenotypic change.

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