Dr Timothy Davies
(email at email@example.com)
Cell division varies with cell identity
Cytokinesis is the process by which one cell physically divides into two at the end of mitosis. This process is fundamental for life, and errors can result in abnormal chromosomal numbers, developmental defects, and cancers. Work over the last century has shown that cytokinesis in animal cells requires a carefully synchronised set of molecular signals that promote the formation of a contractile ring around the cell equator, which then constricts to divide the cell. Similarities in the structural and molecular organization of this division apparatus in a variety of animal model systems give the impression that the mechanisms underlying cell division do not vary between cell and organism types. However, clinical studies have shown tissue-specific division failure due to mutations in cytokinetic proteins. In addition to this, we have shown that in the early Caenorhabditis elegans embryo the requirement for an ‘essential’ cytokinesis protein varies between specific cells. These results highlight an under-appreciated intersection between cell identity and cell division. Therefore, our lab is expanding work in this area, analysing cell division in a multicellular context to identify how cells from the same organism are regulated in different ways during cytokinesis.
C. elegans is an ideal tool to study cell division
Caenorhabditis elegans is a small (1mm) nematode worm that has several characteristics that make it an excellent model in which to investigate context-specific variation in cell division. First, it has a stereotyped development in which each cell has a different identity, allowing cytokinetic phenotypes to be compared between different cells. Second, C. elegans has been used as a model system for decades and many of the pathways that contribute to specifying cell fate during development are well known. Third, genetic tools allow us to precisely disrupt or modify specific protein function. Fourth, cell division and embryogenesis can be observed using live-cell fluorescence microscopy, allowing analysis and quantification of these dynamic processes. Finally, many pathways involved in cytokinesis and cell identity are highly conserved between C. elegans and higher metazoans, which enables comparison with other model systems. Taking advantage of these features, our lab currently investigates how cytokinesis varies between cells in the early C. elegans embryo using a combination of genetics and fluorescence microscopy.
- Animal Cells and Systems
- C. elegans development
- Cell division
- Cytoskeletal structure and dynamics
- Live-cell fluorescence microscopy
- Davies, Tim, Kim, Han X, Romano Spica, Natalia, Lesea-Pringle, Benjamin J, Dumont, Julien, Shirasu-Hiza, Mimi & Canman, Julie C (2018). Cell-intrinsic and -extrinsic mechanisms promote cell-type-specific cytokinetic diversity. eLife 7: e36204.
- Hirsch, Sophia M., Sundaramoorthy, Sriramkumar, Davies, Tim, Zhuravlev, Yelena, Waters, Jennifer C., Shirasu-Hiza, Mimi, Dumont, Julien & Canman, Julie C. (2018). FLIRT: fast local infrared thermogenetics for subcellular control of protein function. Nature Methods 15(11): 921-923.
- Sundaramoorthy, Sriramkumar, Garcia Badaracco, Adrian, Hirsch, Sophia M., Park, Jun Hong, Davies, Tim, Dumont, Julien, Shirasu-Hiza, Mimi, Kummel, Andrew C. & Canman, Julie C. (2017). Low Efficiency Upconversion Nanoparticles for High-Resolution Coalignment of Near-Infrared and Visible Light Paths on a Light Microscope. ACS Applied Materials & Interfaces 9(9): 7929-7940.
- Davies, Tim, Jordan, Shawn N. & Canman, Julie C. (2016). Cell polarity is on PAR with cytokinesis. Cell Cycle 15(10): 1307-1308.
- Jordan, Shawn N., Davies, Tim, Zhuravlev, Yelena, Dumont, Julien, Shirasu-Hiza, Mimi & Canman, Julie C. (2016). Cortical PAR polarity proteins promote robust cytokinesis during asymmetric cell division. The Journal of Cell Biology 212(1): 39-49.
- Davies, Tim, Kodera, Noriyuki, Kaminski Schierle, Gabriele S., Rees, Eric, Erdelyi, Miklos, Kaminski, Clemens F., Ando, Toshio & Mishima, Masanori (2015). CYK4 Promotes Antiparallel Microtubule Bundling by Optimizing MKLP1 Neck Conformation. PLOS Biology 13(4): e1002121.
- Davies, Tim, Jordan, Shawn N., Chand, Vandana, Sees, Jennifer A., Laband, Kimberley, Carvalho, Ana X., Shirasu-Hiza, Mimi, Kovar, David R., Dumont, Julien & Canman, Julie C. (2014). High-Resolution Temporal Analysis Reveals a Functional Timeline for the Molecular Regulation of Cytokinesis. Developmental Cell 30(2): 209.
- Lee, K.-Y., Davies, T. & Mishima, M. (2012). Cytokinesis microtubule organisers at a glance. Journal of Cell Science 125(15): 3495.
- Davies, Tim & Canman, Julie C. (2012). Stuck in the middle: Rac, adhesion, and cytokinesis. The Journal of Cell Biology 198(5): 769.
- Douglas, Max E., Davies, Tim, Joseph, Nimesh & Mishima, Masanori (2010). Aurora B and 14-3-3 Coordinately Regulate Clustering of Centralspindlin during Cytokinesis. Current Biology 20(10): 927.
- Loiseau, P., Davies, T., Williams, L. S., Mishima, M. & Palacios, I. M. (2010). Drosophila PAT1 is required for Kinesin-1 to transport cargo and to maximize its motility. Development 137(16): 2763.
Chapter in book
- Davies, T., Sundaramoorthy, S., Jordan, S.N., Shirasu-Hiza, M., Dumont, J. & Canman, J.C. (2017). Using fast-acting temperature-sensitive mutants to study cell division in Caenorhabditis elegans. In Methods in Cell Biology. Echard, Arnaud Elsevier. 137: 283-306.