Adherens junctions are multiprotein complexes that mediate cellular adhesion and cell-cell communication.. Signaling mediated through cadherins, the transmembrane components of adherens junctions, at sites of cell-cell contact generates cellular responses, such as changes in gene expression and cytoskeletal rearrangements. Alterations in expression or function of cadherins and other functional proteins have been associated with the metastasis of many types of epithelial carcinomas. Therefore, delineation of signal transduction pathways regulated in response to cadherin-based cell adhesion could provide insights into the molecular mechanisms associated with the progression of cancer. The overall goal of this investigation is to study cadherin-based cell adhesion and the processes it regulates using the model system Drosophila melanogaster. Recent studies indicate that the Drosophila protein Armadillo, a key component of the adherens junctions that links cadherins to the actin cytoskeleton, interacts functionally with the non-receptor tyrosine kinase Abelson and its substrate, Enabled, during cell-cell adhesion of epithelial cells. Therefore, genetic and biochemical experiments will be used to analyze the relationship of Armadillo with Abelson and Enabled for cell adhesion during development. Furthermore, microarray analysis will be used to identify target genes regulated in response to cadherin-based adhesion. Identification of even a single target gene will aid m the characterization of pathways that transduce signals from cadherins to the nucleus.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM020797-03
Application #
6628745
Study Section
Cell Development and Function Integrated Review Group (CDF)
Program Officer
Tompkins, Laurie
Project Start
2001-02-01
Project End
Budget Start
2003-02-01
Budget End
2003-04-30
Support Year
3
Fiscal Year
2003
Total Cost
$13,841
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Stevens, Traci L; Rogers, Edward M; Koontz, Laura M et al. (2008) Using Bcr-Abl to examine mechanisms by which abl kinase regulates morphogenesis in Drosophila. Mol Biol Cell 19:378-93
Grevengoed, E E; Loureiro, J J; Jesse, T L et al. (2001) Abelson kinase regulates epithelial morphogenesis in Drosophila. J Cell Biol 155:1185-98