DYNAmics of CrossOver designation
The DYNACO project aims to investigate the dynamics of crossover formation and interference in meiosis using super-resolution microscopy and genetic tools in Sordaria macrospora, enhancing our understanding and potential manipulation of recombination.
Projectdetails
Introduction
Meiotic crossovers make us unique. Their distribution along chromosomes dictates which traits will be reassorted to create new and unique allele combinations on which selection can act. Early during meiosis, a large number of recombination interactions are initiated all across the genome, but only a few ultimately mature into crossovers. The final number and positions of crossovers are tightly regulated: along each chromosome, crossovers tend to be evenly spaced.
Crossover Interference
This phenomenon, called crossover interference, was discovered in 1914 by Sturtevant and Morgan while drawing the first recombination map in flies. Emergence of spatial patterning requires communication. But how does the crossover formation machinery communicate with neighboring crossovers half a chromosome away?
Challenges in Understanding Communication
Our understanding of how this communication is established has been hindered by the limited resolution in time provided by classical cytology, giving us access to only snapshots of the process.
Project Overview
In the DYNACO project, I will develop innovative solutions to explore the dynamics of crossover designation and interference. Using gentle live super-resolution microscopy combined with groundbreaking genetic and optogenetic tools in a very amenable system, the filamentous fungus Sordaria macrospora, I will address the following questions:
- How do pro-crossover factors behave dynamically to enact and respond to crossover interference?
- What is the medium supporting crossover communication?
- What are the consequences of locally disrupting this communication?
Expected Outcomes
The DYNACO project will provide fundamental breakthroughs in our understanding of crossover formation, designation, and interference. We will confront and reconcile many aspects of current models for crossover interference and develop our own unified model. This work also has the potential to provide tools for the manipulation of recombination, to accelerate the introgression of selective traits into elite crop genomes.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.562.501 |
Totale projectbegroting | € 1.562.501 |
Tijdlijn
Startdatum | 1-3-2024 |
Einddatum | 28-2-2029 |
Subsidiejaar | 2024 |
Partners & Locaties
Projectpartners
- CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRSpenvoerder
Land(en)
Vergelijkbare projecten binnen European Research Council
Project | Regeling | Bedrag | Jaar | Actie |
---|---|---|---|---|
Unraveling the regulation of crossover formation from its in vivo dynamicsThis project aims to elucidate the regulatory mechanisms of crossover formation during meiosis using advanced imaging and AI analysis in C. elegans and zebrafish to enhance understanding of genetic diversity and integrity. | ERC Consolid... | € 2.558.835 | 2025 | Details |
Meiotic adaptation to allopolyploidyThis project aims to investigate the molecular mechanisms ensuring meiotic stability in nascent allopolyploids by recreating hybridization events and characterizing recombination processes. | ERC Starting... | € 1.496.630 | 2024 | Details |
Nuclear cooperation and conflict across symbiotic fungal networksThis project investigates the genetic diversity and reproductive mechanisms of arbuscular mycorrhizal fungi to enhance nutrient exchange in plant networks and challenge existing evolutionary theories. | ERC Starting... | € 1.500.000 | 2023 | Details |
Recreating molecular memories: imaging the mechanics of chromosome assembly and the birth of cell identityThis project aims to uncover the molecular mechanisms of histone deposition during DNA replication to enhance understanding of epigenetic memory transmission and chromosome assembly. | ERC Consolid... | € 1.999.575 | 2025 | Details |
Cracking the Post-Translational Modification Crosstalk Code in S. cerevisiaeThis project aims to systematically investigate post-translational modification crosstalk in S. cerevisiae using CRISPR-based methods to uncover regulatory mechanisms across biological processes. | ERC Starting... | € 1.489.798 | 2025 | Details |
Unraveling the regulation of crossover formation from its in vivo dynamics
This project aims to elucidate the regulatory mechanisms of crossover formation during meiosis using advanced imaging and AI analysis in C. elegans and zebrafish to enhance understanding of genetic diversity and integrity.
Meiotic adaptation to allopolyploidy
This project aims to investigate the molecular mechanisms ensuring meiotic stability in nascent allopolyploids by recreating hybridization events and characterizing recombination processes.
Nuclear cooperation and conflict across symbiotic fungal networks
This project investigates the genetic diversity and reproductive mechanisms of arbuscular mycorrhizal fungi to enhance nutrient exchange in plant networks and challenge existing evolutionary theories.
Recreating molecular memories: imaging the mechanics of chromosome assembly and the birth of cell identity
This project aims to uncover the molecular mechanisms of histone deposition during DNA replication to enhance understanding of epigenetic memory transmission and chromosome assembly.
Cracking the Post-Translational Modification Crosstalk Code in S. cerevisiae
This project aims to systematically investigate post-translational modification crosstalk in S. cerevisiae using CRISPR-based methods to uncover regulatory mechanisms across biological processes.