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MorphoPace: Understanding the conserved mechanisms pacing morphogenesis

Project description

Embryonic development timing in fish

During development, the embryo undergoes a coordinated biological process that involves cell differentiation and morphogenesis. While our understanding of the molecular control of cell differentiation is improving, the mechanism and timing of morphogenetic movements remain less clear. With the support of the Marie Skłodowska-Curie Actions programme, the MorphoPace project aims to delineate gastrulation, a critical early morphogenetic event. To identify the timing and pace of gastrulation, researchers will investigate different fish species, characterise cell and tissue dynamics, and study the role of the environment. Collectively, the work will improve our understanding of key developmental processes.

Objective

Animal development relies on the timely succession of different differentiation, in which cells acquire a certain identity and function, and morphogenetic, in which cells are placed in the part of the animal body, steps. These conserved steps follow a highly stereotypical timing among animals of the same species, but, remarkably, it varies significantly across species. For example, gastrulation, the first morphogenetic movement shaping the embryo, takes 2.5x longer in medaka (Oryzias latipes) than zebrafish (Danio rerio) in the same conditions. Although these differences are well known, it remains unclear how time is kept during development. Recent work has shown that molecular differences between species define the pace of differentiation. It is unclear, however, how these scale up to set the pace of morphogenesis, a collective process that happens across embryos, and set by active cell movements and resisting tissue material properties. With this project, I aim to understand these pace morphogenesis, by comparing gastrulation in two fish species: zebrafish and medaka. Since the latter species remains undescribed, I will first characterize mesendoderm internalization, the opening act of gastrulation. I will map single-cell properties and tissue-scale features, and use a theoretical physics model to make predictions about timing differences between species. Secondly, I will define whether pace is intrinsic to the cells, or set by the native environment, by transplanting cells between embryos of different species, and using zebrafish-medaka hybrids. Finally, I will manipulate the pace of internalization by modulating both intrinsic forces and the tissue state. Altogether, this project will build a way to understand morphogenesis by comparing different fish species, which have broad implications in biology, physics and evolution by uncovering how embryos time development across teleost fish, the largest and most diverse class of vertebrates in the planet.

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HORIZON-TMA-MSCA-PF-EF - HORIZON TMA MSCA Postdoctoral Fellowships - European Fellowships

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Call for proposal

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(opens in new window) HORIZON-MSCA-2024-PF-01

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Coordinator

FORSCHUNGSINSTITUT FUR MOLEKULARE PATHOLOGIE GESELLSCHAFT MBH
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 214 344,72
Address
CAMPUS-VIENNA-BIOCENTER 1
1030 Wien
Austria

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Region
Ostösterreich Wien Wien
Activity type
Private for-profit entities (excluding Higher or Secondary Education Establishments)
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Total cost

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