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BRIDGE: Uncovering the biological relevance of non-paralogous gene-gene loops in coordinating transcription and function across neurons and other cell types

Project description

Characterising the role of non-paralogous gene-gene loops

Recent research into 3D genome architecture reveals that specific genes physically interact across large genomic distances. However, it remains unclear whether these interactions coordinate activity across multiple genes. Supported by the Marie Skłodowska-Curie Actions programme, the BRIDGE project aims to investigate how physical interactions between distant, non-paralogous genes (gene-gene loops) influence transcriptional programmes and whether they occur exclusively in neurons. To do so, it will study long-range, pairwise gene contacts in fly neurons and other cell types, testing whether they coordinate gene transcription and function. The findings could uncover new disease mechanisms in mammals and explain how genome structures regulate multiple genes, leading to the discovery of advanced gene therapies.

Objective

Gene transcription is tightly controlled by regulatory elements in the genome. While most act locally, distant regulatory elements are increasingly recognized as key contributors to gene control, revising our fundamental understanding of how regulatory interactions are organized in genomes. Recent three-dimensional (3D) genome folding studies showed that some genes form specific, long-range physical contacts with other gene loci. However, whether such contacts coordinate multi-gene activity remains unknown.

My BRIDGE (Biological Regulation of Interacting Distant GEnes) project investigates ultra-long-range, pairwise gene contacts recently discovered in fly neurons. These gene pairs are not known to function together but engage in highly specific and conserved contacts. Using the simplicity of these contacts and their suitability for in vivo manipulation, this project will test whether these distant gene contacts coordinate gene transcription and function in neurons and other cell types.

Through genome engineering, chromatin imaging, genomics and genetic assays, I will disrupt or rewire these contacts (WP1-3) and analyze their biological impact. WP4 will explore whether these contacts extend beyond neurons by comparing 3D genome organization across four differentiated cell types from all germ layers.

BRIDGE will determine whether long-range gene tethering is a neuron-specific or broader regulatory mechanism. It may also uncover novel functional synergies between mammalian disease-relevant homologs of the studied genes. More broadly, BRIDGE will deepen our understanding of how genome organization enables multi-gene regulation, with long-term implications for developing gene therapies targeting gene networks. It will also provide interdisciplinary training and career development to support my transition to independent research at the interface of 3D genomics and gene regulation.

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

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

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Call for proposal

(opens in new window) HORIZON-MSCA-2025-PF

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Coordinator

UNIVERSITE DE LAUSANNE
Net EU contribution
€ 307 958,88
Address
QUARTIER UNIL CENTRE - BATIMENT UNICENTRE
1015 LAUSANNE
Switzerland
Region
Schweiz/Suisse/Svizzera Région lémanique Vaud
Activity type
Higher or Secondary Education Establishments
Links
Total cost
No data