Structural Basis for Centromere-Mediated Control of Error-free Chromosome Segregation
This project aims to elucidate the mechanisms of chromosome segregation by studying the assembly and function of inner centromeres and their regulatory networks using advanced structural and functional techniques.
Projectdetails
Introduction
Accurate chromosome segregation during cell division requires bipolar attachment of sister chromatids to microtubules emanating from opposite spindle poles and maintenance of sister-chromatid cohesion until all chromosomes achieve bi-orientation.
Chromosomal Regulation
Two chromosomal sites regulate these processes:
- Centromeres: The microtubule attachment sites defined by the enrichment of CENP-A nucleosomes.
- Inner Centromere: A region between the sister chromatids that recruits enzymatic activities (kinases, phosphatases, and motor proteins).
The inner centromere associated enzymes selectively stabilize chromosome-microtubule attachments suitable for chromosome bi-orientation, control sister chromatid cohesion, and achieve timely chromosome segregation.
Consequences of Errors
Errors in these processes can lead to aneuploidy, a numerical chromosomal aberration implicated in miscarriages, birth defects, and cancers.
Research Approach
Using an integrative structure-function approach (X-ray crystallography, cryo-electron microscopy, Crosslinking/Mass Spectrometry, biochemical/biophysical methods with human cell-line based functional assays), we will obtain detailed mechanistic understanding of:
- How the inner centromere is assembled.
- How the inner centromere associated interaction network recruits regulators to achieve chromosome bi-orientation and accurate segregation.
- How centromere identity is maintained through multiple generations.
Significance of the Work
This work builds on our recently obtained exciting structural/molecular knowledge that has led to unexpected insights and new questions and will exploit our recently generated battery of molecular reagents.
The outcome of our work will provide unprecedented details of centromere-mediated control of chromosome segregation and allow us to build a comprehensive mechanistic model for error-free chromosome segregation, a process that has been fascinating researchers for more than a century.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 2.209.886 |
Totale projectbegroting | € 2.209.886 |
Tijdlijn
Startdatum | 1-3-2023 |
Einddatum | 29-2-2028 |
Subsidiejaar | 2023 |
Partners & Locaties
Projectpartners
- LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHENpenvoerder
- THE UNIVERSITY OF EDINBURGH
Land(en)
Vergelijkbare projecten binnen European Research Council
Project | Regeling | Bedrag | Jaar | Actie |
---|---|---|---|---|
Sequence-structure-function: uncovering how genetic variation at human centromere drives cellular phenotypesThis project aims to investigate centromere variation's mutagenic processes and functional impacts on genome stability and disease predisposition using a multidisciplinary approach. | ERC Starting... | € 1.500.000 | 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 |
Mechanisms of cellular response to errors in mitosis: a new, non-genetic approach to an old questionThis project aims to investigate how mitotic errors and nuclear abnormalities influence cellular homeostasis and tumorigenesis through non-genetic mechanisms, utilizing advanced genomic and imaging techniques. | ERC Starting... | € 1.498.111 | 2024 | 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 |
Spatiotemporal regulation of centriolar satellite homeostasisThis project aims to investigate the molecular mechanisms of centriolar satellites, exploring their assembly, dynamics, and role in cellular processes to enhance understanding of membrane-less organelle function. | ERC Starting... | € 1.588.710 | 2023 | Details |
Sequence-structure-function: uncovering how genetic variation at human centromere drives cellular phenotypes
This project aims to investigate centromere variation's mutagenic processes and functional impacts on genome stability and disease predisposition using a multidisciplinary approach.
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.
Mechanisms of cellular response to errors in mitosis: a new, non-genetic approach to an old question
This project aims to investigate how mitotic errors and nuclear abnormalities influence cellular homeostasis and tumorigenesis through non-genetic mechanisms, utilizing advanced genomic and imaging techniques.
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.
Spatiotemporal regulation of centriolar satellite homeostasis
This project aims to investigate the molecular mechanisms of centriolar satellites, exploring their assembly, dynamics, and role in cellular processes to enhance understanding of membrane-less organelle function.