Associate Professor, Biochemistry & Molecular Biology
Colorado State University
Precise regulation of mitosis is critical so that the resulting daughter cells have exactly one copy of each chromosome, since mis-segregation of chromosomes is implicated in the formation of birth defects and in the initiation and progression of cancer. Kinetochores — large protein structures assembled upon centromeric chromatin — serve as key orchestrators of mitosis. These structures connect chromosomes to spindle microtubules through the NDC80 complex, the “core” kinetochore-microtubule attachment factor. Controlled changes in kinetochore-microtubule attachment stability allow for correction of erroneous attachments in early mitosis, and force generation for chromosome movements in late mitosis. Importantly, the status of kinetochore-microtubule attachment is continually relayed to the spindle assembly checkpoint so that mitosis is arrested if kinetochores are not stably attached to microtubules, and a mitotic exit program is initiated when stable attachment is achieved. Using a combination of cell biological approaches, in vitro biochemical reconstitution, and mathematical modeling, our lab is currently investigating how kinetochore-microtubule attachments are regulated and monitored during mitosis to ensure accurate chromosome segregation.
Tauchman EC, Boehm F, and DeLuca JG (2015). Stable kinetochore-microtubule attachment is sufficient to silence the spindle assembly checkpoint in human cells. Nature Communications 6:10036. [PMC4686653]
Zaytsev AV, Sundin LJR, DeLuca KF, Grishchuk EL, and DeLuca JG (2014). Accurate phosphoregulation of kinetochore-microtubule affinity requires unconstrained molecular interactions. Journal of Cell Biology 206:45-59. [PMC4085703]