We are interested in understanding the mechanism of how eukaryotic cells inherit their genetic material accurately at each round of cell division. We focus on the kinetochore, the macromolecular protein complex that drives chromosome segregation. Although it was widely believed that the structural core of kinetochores would be composed of proteins that are conserved in all eukaryotes (e.g. CENP-A, Ndc80), we discovered an unconventional class of kinetochore proteins (KKT1–25) in Trypanosoma brucei, an evolutionarily-divergent kinetoplastid parasite. Our current goal is to understand how they carry out conserved kinetochore functions such as binding to DNA or microtubules, as well as establishment of proper bi-oriented attachments. We also reconstitute kinetochore complexes and characterize them using various approach, including structural biology and biophysics. By understanding the unique kinetoplastid kinetochores, we aim to reveal fundamental principles of chromosome segregation mechanism in eukaryotes. If you are interested in joining us, please contact us!
- How is kinetochore position specified without CENP-A?
- How is kinetochore assembled without CENP-A? Regulation?
- Which proteins bind DNA? How? Regulation?
- Which proteins bind microtubules? How? Regulation?
- Which proteins interact with which ones? Regulation?
- How do kinetoplastid kinetochores achieve bi-orientation?
- What is the structure and origin of kinetoplastid kinetochore proteins?
- What is the structure of kinetoplastid kinetochores in cells?
- Can we isolate native kinetoplastid kinetochores?
- Can we target KKT proteins to prevent the growth of kinetoplastid parasites?
Our research is supported by
Boehringer Ingelheim Fonds
Previously supported by
Royal Society, John Fell Fund, EPA CEPHALOSPORIN FUND, Toyobo Biotechnology Foundation Fellowship, Uehara Memorial Foundation Fellowship, Wellcome-Beit Prize Fellowship, HFSP Long Term Fellowship, EMBO Long Term Fellowship