We focus on cell division, a process that requires a dramatic and highly orchestrated change in cell structure, including the condensation of chromosomes, their alignment on a bipolar spindle, the synchronous movement of exactly half of the chromosomes to opposite poles of the cell, and then cytokinesis (dividing the cell into two).
To accomplish cell division with high fidelity requires tight control of chromosome structure, including the displacement of proteins that might hinder chromosome segregation, and the recruitment of proteins that allow the chromosomes to condense and be “bi-oriented” on the spindle. Through all of this change, the cell also may retain markers (“bookmarks”) on chromosomes that can “remember” whether genes are active or inactive so that they can be returned to their original states once cell division is complete. These events must be precisely controlled in location and timing. Our laboratory studies these control mechanisms. In particular, we study how chromatin modifications help determine where and when key regulatory factors can bind to chromosomes.
We are particularly interested in how histone kinases such as Haspin and Aurora B control cell division in human cells, how this process contributes to the generation of cancer and birth defects, and how it can be exploited for disease therapy. In the future, we aim to determine the roles of additional histone modifications in mitosis, to explore their functions in meiosis, and to develop a genome-wide understanding of how these marks are deposited to regulate both chromosome segregation and the inheritance of epigenetic information during cell division.