Evolutionary principles of nuclear dynamics and remodelling
This project aims to uncover the genomic and evolutionary factors influencing nuclear dynamics across eukaryotes, enhancing our understanding of karyodynamic diversity and its evolutionary origins.
Projectdetails
Introduction
Every eukaryote has a nucleus, a double lipid membrane-bound compartment that encapsulates the genome, but almost every nucleus is different - in shape, size, molecular composition, spatial organisation, and dynamics through the cell cycle. Given its fundamental and universal functional roles in protecting the DNA and regulating the exchange of information and control machinery between genome and cytoplasm, one might ask the question: why are there so many ways to build and remodel a nucleus?
Research Objectives
Bringing together comparative genomics, phylogenetics, quantitative cell biology, and experimental evolution in multiple microbial model systems drawn from across the eukaryotic tree, we set out to elucidate the genomic, biophysical, and evolutionary factors that determine nuclear dynamics and remodelling - karyodynamics - within the context of cellular architecture and function.
Methodology
A comparative perspective driven by phylogenetics will enable us to:
- Separate universal principles of karyodynamics from species- and niche-specific adaptations.
- Dissect the reasons for the evolutionary and developmental plasticity that we observe experimentally.
Applications
In turn, we can use these principles to infer, predict, and validate phenotypes in novel and emerging model systems.
Conclusion
Finally, a more comprehensive understanding of the mechanisms responsible for karyodynamic phenotypic diversity would allow us to reconstruct evolutionary trajectories all the way back to the origins of the nuclear compartment, a landmark event in the evolution of eukaryotes from an archaeal-bacterial symbiosis over 2 billion years ago.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.615.930 |
Totale projectbegroting | € 1.615.930 |
Tijdlijn
Startdatum | 1-4-2023 |
Einddatum | 31-3-2028 |
Subsidiejaar | 2023 |
Partners & Locaties
Projectpartners
- EUROPEAN MOLECULAR BIOLOGY LABORATORYpenvoerder
Land(en)
Vergelijkbare projecten binnen European Research Council
Project | Regeling | Bedrag | Jaar | Actie |
---|---|---|---|---|
Dependence Of NUcleosome Transactions on SequenceDevelop a novel high-throughput platform to investigate how DNA sequence influences chromatin remodelling dynamics and nucleosome function at the single-molecule level. | ERC Advanced... | € 2.137.145 | 2023 | Details |
Mechanisims of nuclear self-assemblyThe project aims to create synthetic nuclei ('Organelloids') to study the self-assembly mechanisms of the nuclear envelope, enhancing understanding of nuclear function and its implications for diseases. | ERC Starting... | € 1.499.974 | 2024 | Details |
Reshaping the nucleome to reveal its gene- and mechano-regulatory functionThe RENOME project aims to develop tools for real-time study and reengineering of chromatin organization to connect nuclear mechanics with cellular behavior and inform future epigenetic therapies. | ERC Consolid... | € 1.998.595 | 2025 | Details |
Illuminating radial genome organization in the nucleusThis project aims to explore the universal radial GC-gradient in mammalian cell genomes, developing methods to understand its role in nuclear organization and function across species and conditions. | ERC Consolid... | € 1.999.655 | 2024 | Details |
Revealing the structure and mechanism of mitotic chromosome folding inside the cellThis project aims to elucidate the folding principles of mitotic chromosomes in single human cells using advanced imaging techniques to enhance understanding of genome restructuring during cell division. | ERC Advanced... | € 3.118.430 | 2024 | Details |
Dependence Of NUcleosome Transactions on Sequence
Develop a novel high-throughput platform to investigate how DNA sequence influences chromatin remodelling dynamics and nucleosome function at the single-molecule level.
Mechanisims of nuclear self-assembly
The project aims to create synthetic nuclei ('Organelloids') to study the self-assembly mechanisms of the nuclear envelope, enhancing understanding of nuclear function and its implications for diseases.
Reshaping the nucleome to reveal its gene- and mechano-regulatory function
The RENOME project aims to develop tools for real-time study and reengineering of chromatin organization to connect nuclear mechanics with cellular behavior and inform future epigenetic therapies.
Illuminating radial genome organization in the nucleus
This project aims to explore the universal radial GC-gradient in mammalian cell genomes, developing methods to understand its role in nuclear organization and function across species and conditions.
Revealing the structure and mechanism of mitotic chromosome folding inside the cell
This project aims to elucidate the folding principles of mitotic chromosomes in single human cells using advanced imaging techniques to enhance understanding of genome restructuring during cell division.