Summary
Thousands of Conserved Non-coding Elements (CNEs) are shared by jawed vertebrates, some of which were shown to be important developmental enhancers. However, how these intriguing elements evolve at the functional level and why they are so conserved in sequence remain some of the biggest mysteries in the field of regulatory genomics. In this project, I build a novel view of CNE function and evolution based on my preliminary data and recent breakthroughs on enhancer pleiotropy. This working hypothesis posits that CNEs are ancient transcription factor binding hubs that act as dynamic multi-genic regulators to which new gene targets can be added/removed during evolution. Taking advantage of the exceptional conservation of CNEs, I propose the experimental framework to test this hypothesis on orthologous elements across major vertebrate clades using cutting-edge methodology combining Capture-HiC, RNA-seq and ATAC-seq in shark, chicken and mouse. This approach will provide comparative CNE-target contact maps that will reveal conserved as well as gained and lost interactions in each species, whose functional impact will be tested using CRISPR knockout and interference in mouse neuronal differentiation. In summary, this project will address long-standing questions on the evolution of the regulatory genome and offer insights into the flexibility of enhancers to acquire and lose targets in evolution, expanding our understanding on the pervasiveness and evolution of regulatory pleiotropy.
Unfold all
/
Fold all
More information & hyperlinks
| Web resources: | https://cordis.europa.eu/project/id/101152740 |
| Start date: | 01-05-2025 |
| End date: | 30-04-2027 |
| Total budget - Public funding: | - 165 312,00 Euro |
Cordis data
Original description
Thousands of Conserved Non-coding Elements (CNEs) are shared by jawed vertebrates, some of which were shown to be important developmental enhancers. However, how these intriguing elements evolve at the functional level and why they are so conserved in sequence remain some of the biggest mysteries in the field of regulatory genomics. In this project, I build a novel view of CNE function and evolution based on my preliminary data and recent breakthroughs on enhancer pleiotropy. This working hypothesis posits that CNEs are ancient transcription factor binding hubs that act as dynamic multi-genic regulators to which new gene targets can be added/removed during evolution. Taking advantage of the exceptional conservation of CNEs, I propose the experimental framework to test this hypothesis on orthologous elements across major vertebrate clades using cutting-edge methodology combining Capture-HiC, RNA-seq and ATAC-seq in shark, chicken and mouse. This approach will provide comparative CNE-target contact maps that will reveal conserved as well as gained and lost interactions in each species, whose functional impact will be tested using CRISPR knockout and interference in mouse neuronal differentiation. In summary, this project will address long-standing questions on the evolution of the regulatory genome and offer insights into the flexibility of enhancers to acquire and lose targets in evolution, expanding our understanding on the pervasiveness and evolution of regulatory pleiotropy.Status
SIGNEDCall topic
HORIZON-MSCA-2023-PF-01-01Update Date
22-11-2024
Images
No images available.
Geographical location(s)
