This investigator has made significant contributions to the understanding of cytokinesis. The mechanisms responsible for completing cytokinesis remain poorly defined. During the current period of support the applicant performed a genetic screen to identify novel proteins involved in cytokinesis. Two genes were identified. The first is racE, a small GTPase that appears to be an important signalling molecule required for cytokinesis. The second gene, called lvsA, has homology to the murine beige and the human FAN proteins, and is also required for cytokinesis. The current application builds on these findings with aims to dissect the role these two genes play in cytokinesis.
Three specific aims are proposed: (1) to determine the role racE plays in cytokinesis, (2) to determine what other molecules interact with racE, and (3) to determine the role lvsA plays in cytokinesis.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM048745-07
Application #
2857174
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1993-01-01
Project End
1999-08-31
Budget Start
1999-01-01
Budget End
1999-08-31
Support Year
7
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Duke University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Falkenstein, Kristin; De Lozanne, Arturo (2014) Dictyostelium LvsB has a regulatory role in endosomal vesicle fusion. J Cell Sci 127:4356-67
Kypri, Elena; Falkenstein, Kristin; De Lozanne, Arturo (2013) Antagonistic control of lysosomal fusion by Rab14 and the Lyst-related protein LvsB. Traffic 14:599-609
Wen, Yujia; Stavrou, Irene; Bersuker, Kirill et al. (2009) AP180-mediated trafficking of Vamp7B limits homotypic fusion of Dictyostelium contractile vacuoles. Mol Biol Cell 20:4278-88