Recruitment and activation of SLK at the leading edge of migrating cells requires Src family kinase activity and the LIM-only protein 4
- Author(s)
- Baron, KD; Al-Zahrani, K; Conway, J; LaBreche, C; Storbeck, CJ; Visvader, JE; Sabourin, LA;
- Journal Title
- Biochim Biophys Acta
- Publication Type
- Journal Article in press
- Abstract
- The Ste20-like kinase SLK plays a pivotal role in cell migration and focal adhesion turnover and is regulated by the LIM domain-binding proteins Ldb1 and Ldb2. These adapter proteins have been demonstrated to interact with LMO4 in the organization of transcriptional complexes. Therefore, we have assessed the ability of LMO4 to also interact and regulate SLK activity. Our data show that LMO4 can directly bind to SLK and activate its kinase activity in vitro and in vivo. LMO4 can be co-precipitated with SLK following the induction of cell migration by scratch wounding and Cre-mediated deletion of LMO4 in conditional LMO4fl/fl fibroblasts inhibits cell migration and SLK activation. Deletion of LMO4 impairs Ldb1 and SLK recruitment to the leading edge of migrating cells. Supporting this, Src/Yes/Fyn-deficient cells (SYF) expressing very low levels of LMO4 do not recruit SLK to the leading edge. Re-expression of wildtype Myc-LMO4 in SYF cells, but not a mutant version, restores SLK localization and kinase activity. Overall, our data suggest that activation of SLK by haptotactic signals requires its recruitment to the leading edge by LMO4 in a src-dependent manner. Furthermore, this establishes a novel cytosolic role for the transcriptional co-activator LMO4.
- Publisher
- Elsevier
- Research Division(s)
- Stem Cells And Cancer
- PubMed ID
- 25882817
- Publisher's Version
- https://doi.org/10.1016/j.bbamcr.2015.04.003
- Terms of Use/Rights Notice
- Refer to copyright notice on published article.
Creation Date: 2015-05-20 10:11:18
Last Modified: 2015-05-20 11:31:30