During development intercellular adhesion and the cytoskeleton must be regulated to accommodate the changes in cell shape, cell rearrangements and cell migrations that occur as the embryo is shaped. If they are not properly regulated, morphogenesis is disrupted and normal development fails. Furthermore, during the progression of most tumors, cell adhesion is reduced or lost, ultimately resulting in increased invasiveness and metastatic potential of the tumor. Recent studies have revealed that members of the Ena/VASP protein family not only promote cell adhesion, but also inhibit cell motility by regulating localized actin polymerization. Accordingly, both overexpression and depletion of one of the family members, VASP, leads to neoplastic transformation of fibroblasts. The continued study Ena/VASP function may therefore provide insight into the cellular mechanisms that underlie both morphogenesis and tumorigenesis. However, the presence of three Ena/VASP family members in mammals makes functional studies of these proteins in an intact animal difficult. To circumvent this, the function of Ena/VASP proteins will be examined in the fruit fly, Drosophila, where a single-family member, Enabled (Ena), is expressed. Ena functions during epithelial morphogenesis and cell migration will be defined by examining the consequences of loss of Ena function and Ena overexpression. The proposed role of Ena in promoting actin polymerization during epithelial morphogenesis will also be addressed using cell biological and genetic techniques. Finally, regulators and targets of Ena will be identified using a genetic modifier screen and their function during development characterized.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM068337-02
Application #
6765289
Study Section
Special Emphasis Panel (ZRG1-F05 (20))
Program Officer
Tompkins, Laurie
Project Start
2003-04-04
Project End
2005-06-01
Budget Start
2004-04-04
Budget End
2005-04-03
Support Year
2
Fiscal Year
2004
Total Cost
$47,296
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Gates, Julie; Nowotarski, Stephanie H; Yin, Hongyan et al. (2009) Enabled and Capping protein play important roles in shaping cell behavior during Drosophila oogenesis. Dev Biol 333:90-107
Gates, Julie; Mahaffey, James P; Rogers, Stephen L et al. (2007) Enabled plays key roles in embryonic epithelial morphogenesis in Drosophila. Development 134:2027-39
Grevengoed, Elizabeth E; Fox, Donald T; Gates, Julie et al. (2003) Balancing different types of actin polymerization at distinct sites: roles for Abelson kinase and Enabled. J Cell Biol 163:1267-79