Shedding light on three-dimensional gene regulation
This project aims to elucidate gene expression regulation during differentiation using an ultra-fast optogenetic system and high-resolution genomic tools to study 3D chromatin interactions.
Projectdetails
Introduction
The orchestration of precise gene expression patterns during differentiation and development is dependent on the cis-regulatory elements of the genome, which interact and communicate in three-dimensional (3D) chromatin structures. It is not well understood how these interactions are formed and influence gene expression.
Challenges in Current Research
Our ability to identify the molecular mechanisms involved is hampered by a lack of tools that provide control over the function of regulatory proteins with high temporal precision and that measure 3D chromatin interactions at high resolution.
Project Overview
In this project, we will overcome these hurdles by utilizing an ultra-fast optogenetic system that allows for efficient and reversible nuclear depletion of mammalian proteins upon blue light exposure.
Methodology
We will combine this approach with a range of high-resolution genomic tools to investigate the context-specific functions of:
- Transcription factors
- Co-activators
- Architectural proteins
This investigation will take place throughout erythroid differentiation.
Unique Approach
Importantly, our set-up does not only allow for characterization of acute protein depletion, but also enables us to map the molecular events triggered by the restoration of regulatory proteins to the nucleus. This unique approach will therefore provide detailed insight into their molecular functions.
Proteomics Integration
Moreover, to get a more complete overview of the proteins involved in gene activation, we will implement a locus-specific proteomics approach that enables unbiased identification of the proteome of regulatory regions.
Potential Impact
This innovative integrated research program has strong potential to transform our understanding of the molecular mechanisms that shape the genome and drive gene activation during cellular differentiation. Furthermore, it will lead to the development of cutting-edge tools to analyze gene regulation in its 3D context at high temporal and spatial resolution.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.500.000 |
Totale projectbegroting | € 1.500.000 |
Tijdlijn
Startdatum | 1-1-2024 |
Einddatum | 31-12-2028 |
Subsidiejaar | 2024 |
Partners & Locaties
Projectpartners
- MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EVpenvoerder
Land(en)
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