Andrew Swan

Andrew Swan, Ph.D.
Associate Professor
Dept. Biological Sciences
University of Windsor

Tel: (519) 253-3000 ext. 2730


Research Overview

We use the fruit fly, Drosophila melanogaster, as a model system for studying how the cell cycle is regulated and modified in development. Our work focuses on two major themes:

1) Role of the SCF-Skp2 ubiquitin ligase in maintaining genome stability.
A major focus of our lab is on the regulation of S-phase in the cell cycle. The entry into S-phase is the most carefully regulated decision made by the cell, and a large number of the known oncogenes and tumour suppressors act at this point. The SCF complex plays a critical role in S-phase regulation, functioning both as a tumour suppressor and as an oncogene in different contexts. We have focused on the less understood tumour suppressive roles of SCF-Skp2. We found that loss of Skp2 or an interacting protein, Cks85A results in inappropriate DNA replication and consequent genome instability in Drosophila. To determine how this complex maintains genome stability, are characterizing interacting proteins and ubiquitinated targets of the SCF-Skp2, employing a combined biochemical and genetic approach.

2) Spatial and temporal control of cell cycle transitions in meiosis and embryogenesis.
One of our major focuses is on female meiosis and the ensuing mitotic cell cycles of early embryogenesis. These two cell cycle programs are very different from each other and from the typical cell cycle. Meiosis is the most complex and atypical of all cell divisions, and requires a major retooling of the cell cycle machinery that is still not well understood. The early embryonic cell cycle in contrast, is a pared-down, largely unregulated cell cycle, consisting of only S-phase and mitosis. Though these cell cycle programs are very different from each other, they occur within minutes of each other in a common cytoplasm, utilizing a common pool of cell cycle regulators that are deposited into the egg during oogenesis. These unique constraints mean that cell cycle regulators must be under very sophisticated temporal and spatial control. We are using a combination of approaches to examine how female meiosis and the early embryonic divisions are regulated.


  • Batiha, O., and Swan, A. (2012). Evidence that the spindle assembly checkpoint does not regulate APC(Fzy) activity in Drosophila female meiosis. Genome 55, 63-67.
  • Swan, A. editor. (2012). Meiosis: Molecular mechanisms and cytogenetic diversity (InTech Publishers).
  • Ghorbani, M., Vasavan, B., Kraja, E., and Swan, A. (2011). Cks85A and Skp2 interact to maintain diploidy and promote growth in Drosophila. Developmental biology 358, 213-223.
  • Swan, A. and Schüpbach, T. (2007). The Cdc20 (Fzy)/Cdh1-related protein, Cort, cooperates with Cdc20/Fzy in cyclin destruction and anaphase progression in meiosis I and II in Drosophila. Development 134, 891-9.
  • Wehr, K., Swan, A. and Schupbach, T. (2006). Deadlock, a novel protein of Drosophila, is required for germline maintenance, fusome morphogenesis and axial patterning in oogenesis and associates with centrosomes in the early embryo. Dev Biol 294, 406-17.
  • Swan, A. and Schupbach, T. (2005). Drosophila Female Meiosis and Embryonic Syncytial Mitosis Use Specialized Cks and CDC20 Proteins for Cyclin Destruction. Cell Cycle 4, 1332-1334.
  • Swan, A., Barcelo, G. and Schupbach, T. (2005). Drosophila Cks30A interacts with Cdk1 to target Cyclin A for destruction in the female germline. Development 132, 3669-78.