About the Project
Faithful cell division ensures the correct segregation of the genetic material over multiple generations. Failure of this process may result in cell death or lay the foundation for tumorigenesis. An important prerequisite for successful chromosome segregation and maintenance of genomic integrity is the correct attachment of the chromosomes to microtubules, enabling faithful partitioning of the genetic material. The fidelity of this process is achieved through the combined actions of the so-called error correction process and the spindle assembly checkpoint, crucial molecular safe-guarding mechanisms that jointly eliminate erroneous microtubule-kinetochore attachments and promote bipolar chromosome orientation critical for faithful cell division. In my research group, we aim to understand the molecular mechanisms underpinning the accurate segregation of the chromosomes in mammalian cells, and what aspects of these processes are changed in cancer cells which often have higher, aneuploid, numbers of chromosomes than their non-transformed counterparts.
Dynamic phosphorylation is a particularly important control mechanism for the chromosome segregation process. Pericentromeric Aurora B and kinetochore-localised MPS1 are key mitotic kinases jointly orchestrating error correction and the spindle assembly checkpoint. We now seek to understand how the spatial arrangement of these kinases at different stages of mitosis regulates their interaction and the processes they control. To achieve this, we will employ a combination of biochemical and cell biological techniques, including quantitative fixed and live cell imaging, CRISPR/Cas9-mediated genetic manipulation of cells, in vitro reconstitution assays and protein-protein interaction analysis by mass spectrometry.
Funding Notes
4 Year DPhil Prize Studentships cover full University fees, a tax free enhanced stipend of ~£24,305 pa, and up to £5,300 pa for research costs and travel. The competition is open to applicants from all countries. See View Website for full details and to apply.
References
- Ruza, R.R, Chung, C.W., Gold, D.B.H., Serena, M., Roberts, E., Gruneberg, U. and Barr, F.A. (2025) A pivot-tether model for nucleosome recognition by the chromosomal passenger complex. EMBO Rep. https://doi.org/10.1038/s44319-025-00523-4
- Hayward, D., Roberts, E. and Gruneberg, U. (2022) MPS1 localizes to microtubule-attached kinetochores and actively promotes microtubule release. Curr. Biol. https://www.cell.com/current-biology/fulltext/S0960-9822(22)01695-5
- Hayward, D., Alfonso-Perez, T., and Gruneberg, U. (2019). Orchestration of the spindle assembly checkpoint by CDK1-cyclin B1. FEBS Lett. https://doi.org/10.1002/1873-3468.13591
- Hayward, D., Bancroft, J., Mangat, D., Alfonso-Perez, T., Dugdale, S., McCarthy, J., Barr, F.A., and Gruneberg, U. (2019). Checkpoint signalling and error correction require regulation of the MPS1 T-loop by PP2A-B56. J Cell Biol 218. https://doi.org/10.1083/jcb.201905026
- Hayward, D., Alfonso-Perez, T., Cundell, M.J., Hopkins, M., Holder, J., Bancroft, J., Hutter, L.H., Novak, B., Barr, F.A., and Gruneberg, U. (2019). CDK1-CCNB1 creates a spindle checkpoint-permissive state by enabling MPS1 kinetochore localization. J Cell Biol 218, 1182-1199. https://doi.org/10.1083/jcb.201808014
Find Your Best Opportunity
Tell them AcademicJobs.com sent you!