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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.

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

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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