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Active HORIZON European Commission

Evolutionary Arms Races Shaping the Germline Epigenome

€2M EUR

Funder European Commission
Recipient Organization Institut National de la Sante Et de la Recherche Medicale
Country France
Start Date Apr 01, 2025
End Date Mar 31, 2030
Duration 1,825 days
Number of Grantees 1
Roles Coordinator
Data Source European Commission
Grant ID 101171028
Grant Description

Germline chromatin pathways are key to the stable inheritance of genetic and epigenetic information.

They also participate in intense evolutionary battles between genetic entities with opposite incentives during reproduction.

These include conflicts between transposons and host genomes, between chromosomes during meiosis, and between maternal and paternal epigenomes.

Such genetic conflicts are predicted to drive evolutionary arms races leading to rapid genetic and epigenetic innovations.

Contrary to current dogmas focusing on conserved features, my research program explicitly tackles the functional consequences of epigenome rapid evolution during mammalian reproduction and disease, including in humans.

With the support of the ERC, we want to harvest this unique perspective on the germline epigenome to explore novel inheritance paradigms:(1) Using mouse models, we discovered that rapidly evolving short histone H2A variants function in a novel imprinting-like conflict during reproduction.

We will identify the mechanisms underlying these functions combining epigenome profiling with evolution-guided hypothesis testing in vivo.

We then seek to explore their contributions to reproductive barriers using functional genetics across mouse sub-species.(2) Using in-depth phylogenomics and selection analyses, we uncovered novel signatures of functional diversification in rodent and primate chromatin remodelling enzymes.

We propose to systematically identify these innovations across mammalian germline chromatin pathways.(3) To study the chromatin consequences of these innovations, we designed a surrogate system in human and mouse cells for comparative epigenome profiling.

We will use this approach to uncover the breadth of epigenome regulatory mechanisms shaped by potential genetic conflicts in vivo.

In sum, this proposal interfaces our unique expertise in epigenomics and evolution to transform our current understanding of epigenome regulation and its impact on reproduction.

All Grantees

Institut National de la Sante Et de la Recherche Medicale

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