Direct binding of Talin to Rap1 is required for cell-ECM adhesion in Drosophila
Author:
Affiliation:
1. Department of Cellular and Physiological Sciences, University of British Columbia, Vancouver, Canada, V6T 1Z3
2. School of Biosciences, University of Kent, Canterbury CT2 7NJ, UK
Abstract
Funder
Canadian Institutes of Health Research
Natural Sciences and Engineering Research Council of Canada
Biotechnology and Biological Sciences Research Council
Human Frontier Science Program
Publisher
The Company of Biologists
Subject
Cell Biology
Link
http://journals.biologists.com/jcs/article-pdf/doi/10.1242/jcs.225144/1952803/jcs225144.pdf
Reference51 articles.
1. The BDGP gene disruption project: single transposon insertions associated with 40% of Drosophila genes;Bellen;Genetics,2004
2. Control of cell adhesion dynamics by Rap1 signaling;Boettner;Curr. Opin. Cell Biol.,2009
3. The role of Rap1 in integrin-mediated cell adhesion;Bos;Biochem. Soc. Trans.,2003
4. The N-terminal domains of talin cooperate with the phosphotyrosine binding-like domain to activate beta1 and beta3 integrins;Bouaouina;J. Biol. Chem.,2008
5. Talin is essential for integrin function in Drosophila;Brown;Dev. Cell,2002
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