EXCEED THE SPACE PROVIDED. Cell adhesion is required for embryonic development, wound healing, and the cell-mediated immune response. The interaction of cells with extracellular matrix or other cells influences their polarity, locomotion, proliferation and differentiation. Cytoplasmic proteins that are co-localized with the adhesion receptors are postulated to contribute to the diverse responses of cells to receptor engagement. Zyxin is a LIM-protein that is concentrated at sites of cell-substratum and cell-cell adhesion. It interacts with proteins involved in actin filament assembly and signal transduction. In addition, zyxin shuttles between the nucleus and adhesive membranes; thus it is an excellent candidate for participating in communication between the nuclear and cytoplasmic compartments. Based on these properties, zyxin is postulated to contribute to adhesion-dependent signaling, a process that is central to normal development and that is disturbed in many diseases including cancer. Here we propose to use biochemical, cell biological, and genetic approaches to probe zyxin function. We will analyze the behavior of fibroblasts derived from mice in which the zyxin locus has been disrupted by homologous recombination. These zyxin (-/-) cells will enable us to perform a structure-function analysis of the zyxin protein. Our preliminary results suggest a role/or zyxin in cell migration and signaling; we will define the molecular mechanism by which zyxin contributes to these processes. We will perform experiments designed to elucidate the nuclear function of zyxin. Finally, we will explore the role of zyxin in development by examining the phenotypic consequences of loss of zyxin function in the mouse and the fruit fly. These studies will provide significant new insight into how cells process information coming from cell adhesion receptors to modulate cell behavior. PERFORMANCE SITE ========================================Section End===========================================

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM050877-11
Application #
6829742
Study Section
Special Emphasis Panel (ZRG1-CDF-2 (02))
Program Officer
Deatherage, James F
Project Start
1994-05-01
Project End
2006-11-30
Budget Start
2004-12-01
Budget End
2005-11-30
Support Year
11
Fiscal Year
2005
Total Cost
$358,800
Indirect Cost
Name
University of Utah
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Hoffman, Laura; Jensen, Christopher C; Yoshigi, Masaaki et al. (2017) Mechanical signals activate p38 MAPK pathway-dependent reinforcement of actin via mechanosensitive HspB1. Mol Biol Cell 28:2661-2675
Rosner, Sonia R; Pascoe, Christopher D; Blankman, Elizabeth et al. (2017) The actin regulator zyxin reinforces airway smooth muscle and accumulates in airways of fatal asthmatics. PLoS One 12:e0171728
Piccolo, Stephen R; Hoffman, Laura M; Conner, Thomas et al. (2016) Integrative analyses reveal signaling pathways underlying familial breast cancer susceptibility. Mol Syst Biol 12:860
Stachowiak, Matthew R; Smith, Mark A; Blankman, Elizabeth et al. (2014) A mechanical-biochemical feedback loop regulates remodeling in the actin cytoskeleton. Proc Natl Acad Sci U S A 111:17528-33
Chaturvedi, Aashi; Hoffman, Laura M; Jensen, Christopher C et al. (2014) Molecular dissection of the mechanism by which EWS/FLI expression compromises actin cytoskeletal integrity and cell adhesion in Ewing sarcoma. Mol Biol Cell 25:2695-709
Sankar, Savita; Theisen, Emily R; Bearss, Jared et al. (2014) Reversible LSD1 inhibition interferes with global EWS/ETS transcriptional activity and impedes Ewing sarcoma tumor growth. Clin Cancer Res 20:4584-97
Smith, M A; Hoffman, L M; Beckerle, M C (2014) LIM proteins in actin cytoskeleton mechanoresponse. Trends Cell Biol 24:575-83
Chapin, L M; Edgar, L T; Blankman, E et al. (2014) Mathematical modeling of the dynamic mechanical behavior of neighboring sarcomeres in actin stress fibers. Cell Mol Bioeng 7:73-85
Smith, Mark A; Blankman, Elizabeth; Deakin, Nicholas O et al. (2013) LIM domains target actin regulators paxillin and zyxin to sites of stress fiber strain. PLoS One 8:e69378
Clark, Kathleen A; Kadrmas, Julie L (2013) Drosophila melanogaster muscle LIM protein and alpha-actinin function together to stabilize muscle cytoarchitecture: a potential role for Mlp84B in actin-crosslinking. Cytoskeleton (Hoboken) 70:304-16

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