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Role of three-dimensional genome architecture on innovation through gene duplication in chordates

Project description

3D genome architecture and evolution

Gene duplication is a key evolutionary mechanism responsible for the emergence of new gene functions and traits in some species. Inside the nucleus, DNA is folded into a complex 3D structure that shapes gene activity, but its role in the evolution of new gene functions is not well understood. With the support of the Marie Skłodowska-Curie Actions programme, the CHORDUP project aims to delineate how the 3D genome organisation in chordates impacts gene duplication. Researchers will build a comprehensive atlas linking gene duplications to sequence, expression and spatial genome features. Project findings will improve our understanding of how duplicated genes originate and evolve within their 3D context.

Objective

Inside the nucleus of each eukaryotic cell, DNA is intricately packed into a three-dimensional (3D) structure essential for gene regulation. However, its role in genome evolution, particularly in gene function innovation, remains largely unexplored. Gene duplication is the primary evolutionary path to gene function innovation. This project aims to investigate the interplay between gene duplication evolution and 3D genome structure in chordate genomes by comparing zebrafish to amphioxus, a non-vertebrate marine chordate that diverged from the rest of chordates about 500 million years ago. By generating, for the first time, 3D genome structure maps for several amphioxus organs, I will construct an atlas of gene duplications in zebrafish and amphioxus, encompassing sequence, synteny, gene expression, and 3D genome structure information. Leveraging the information encompassed in this atlas, I will investigate the intricate dynamics between the origin and evolutionary fate of chordate duplicated genes, emerged either by whole-genome or small-scale duplication, and the 3D genome structure around them. By combining my expertise in evolution of gene duplications and amphioxus genomics, with my host group’s experience in 3D genomic architecture and its evolution, we will be able to provide deep insight into the spatial mechanisms of gene innovation through duplication. Studying the effect of 3D genome structure across amphioxus and zebrafish organs in the context of gene duplications, will position me at the forefront of this emerging field within the comparative genomics community. Altogether, the results obtained will enhance our understanding of the evolution of new gene functions, and open new avenues for structural and evolutionary genomics.

Fields of science (EuroSciVoc)

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Topic(s)

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Funding Scheme

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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

UNIVERSITAT AUTONOMA DE BARCELONA
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.

€ 209 914,56
Address
EDIF A CAMPUS DE LA UAB BELLATERRA CERDANYOLA V
08193 Cerdanyola Del Valles
Spain

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Region
Este Cataluña Barcelona
Activity type
Higher or Secondary Education Establishments
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Total cost

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