Skip to main content
Go to the home page of the European Commission (opens in new window)
English en
CORDIS - EU research results
CORDIS

Structural mechanisms of centromeric nucleation of the kinetochore complex

Project description

Kinetochore complex formation on the centromere

When one cell becomes two, genetic material must be separated so that each daughter cell receives its share, a process that is essential to cell division, evolution and disease. In eukaryotes, including humans and yeasts, the chromosomes attach via kinetochore complexes to the spindle-forming microtubules that help separate the DNA. How the inner kinetochore complex is assembled upon centromeric DNA (where the spindle fibres attach to the chromosomes) is poorly understood. With the support of the Marie Skłodowska-Curie Actions programme, the CENStruK project aims to leverage the budding yeast model system with the smallest known kinetochores to investigate kinetochore assembly mechanisms. Biophysical and structural studies using cryo-electron microscopy and cryo-electron tomography will support research efforts.

Objective

Ensuring accurate segregation of the genetic material is an essential life process. In eukaryotes, such as humans and yeasts, regions of DNA known as centromeres nucleate the assembly of the megadalton kinetochore complex, which connects to and regulates spindle-microtubules that drive chromosome segregation. While significant progress has been made in the past decade in understanding the structural architecture of the inner kinetochore Ctf19 complex (CCAN in humans), a fundamental gap in knowledge remains concerning how the inner kinetochore is assembled upon native centromeric DNA. This gap is particularly important, as it addresses critical mechanistic steps involved in maintaining genome integrity across cell divisions, evolution, and disease. The budding yeast Saccharomyces cerevisiae is a fundamental model system for studying centromeres and kinetochores, as its kinetochores, the smallest known, represent the organizational module that, through repeated units, form larger kinetochores like those found in humans. In CENStruK, I will combine my background and expertise in yeast genetics and cell biology with the host lab’s expertise in mechanistic biochemistry, its large collection of proteins involved chromosome segregation, and its advanced electron microscopy facilities to fill this gap. CENStruK is divided into two complementary structural approaches. First, by harnessing required protein chaperones, I will reconstitute a key step in yeast’s inner kinetochore assembly that is required for recognition of its native centromere sequence. Second, I will deploy the ‘CentiCEN’ strain, which houses over 100 homogenized centromeres. This strain will be used in parallel for biophysical and structural studies of the endogenous CEN-kinetochore complex using cryo-EM and cryo-ET. My studies will not only shed light on a fundamental unknown in chromosome biology but will also inform future work in diverse eukaryotic species.

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

HORIZON-TMA-MSCA-PF-EF - HORIZON TMA MSCA Postdoctoral Fellowships - European Fellowships

See all projects funded under this funding scheme

Call for proposal

(opens in new window) HORIZON-MSCA-2024-PF-01

See all projects funded under this call

Coordinator

MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV
Net EU contribution
€ 217 965,12
Address
HOFGARTENSTRASSE 8
80539 MUNCHEN
Germany
Region
Berlin Berlin Berlin
Activity type
Research Organisations
Links
Total cost
No data