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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.

Subsidie
€ 2.209.886
2023

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:

  1. How the inner centromere is assembled.
  2. How the inner centromere associated interaction network recruits regulators to achieve chromosome bi-orientation and accurate segregation.
  3. 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

Startdatum1-3-2023
Einddatum29-2-2028
Subsidiejaar2023

Partners & Locaties

Projectpartners

  • LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHENpenvoerder
  • THE UNIVERSITY OF EDINBURGH

Land(en)

GermanyUnited Kingdom

Inhoudsopgave

European Research Council

Financiering tot €10 miljoen voor baanbrekend frontier-onderzoek via ERC-grants (Starting, Consolidator, Advanced, Synergy, Proof of Concept).

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