TES is a novel focal adhesion protein with a role in cell spreading
Author(s) -
Amanda S. Coutts,
Elaine D. MacKenzie,
Elen Griffith,
Donald M. Black
Publication year - 2003
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.00278
Subject(s) - focal adhesion , biology , microbiology and biotechnology , cytoskeleton , cell adhesion , actin , adhesion , fibronectin , actin cytoskeleton , lim domain , motility , cell migration , cell , gene , genetics , extracellular matrix , signal transduction , chemistry , organic chemistry , zinc finger , transcription factor
Previously, we identified TES as a novel candidate tumour suppressor gene that mapped to human chromosome 7q31.1. In this report we demonstrate that the TES protein is localised at focal adhesions, actin stress fibres and areas of cell-cell contact. TES has three C-terminal LIM domains that appear to be important for focal adhesion targeting. Additionally, the N-terminal region is important for targeting TES to actin stress fibres. Yeast two-hybrid and biochemical analyses yielded interactions with several focal adhesion and/or cytoskeletal proteins including mena, zyxin and talin. The fact that TES localises to regions of cell adhesion suggests that it functions in events related to cell motility and adhesion. In support of this, we demonstrate that fibroblasts stably overexpressing TES have an increased ability to spread on fibronectin.
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