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p190A RhoGAP is a glycogen synthase kinase-3-beta substrate required for polarized cell migration.

Jiang, W, Betson, M, Mulloy, R, Foster, R, Lévay, M, Ligeti, E and Settleman, J (2008) p190A RhoGAP is a glycogen synthase kinase-3-beta substrate required for polarized cell migration. J Biol Chem, 283 (30). pp. 20978-20988.

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Abstract

The Rho GTPases are critical regulators of the actin cytoskeleton and are required for cell adhesion, migration, and polarity. Among the key Rho regulatory proteins in the context of cell migration are the p190 RhoGAPs (p190A and p190B), which function to modulate Rho signaling in response to integrin engagement. The p190 RhoGAPs undergo complex regulation, including phosphorylation by several identified kinases, interactions with phospholipids, and association with a variety of cellular proteins. Here, we have identified an additional regulatory mechanism unique to p190A RhoGAP that involves priming-dependent phosphorylation by glycogen synthase-3-beta (GSK-3beta), a kinase previously implicated in establishing cell polarity. We found that p190A-deficient fibroblasts exhibit a defect in directional cell migration reflecting a requirement for GSK-3beta-mediated phosphorylation of amino acids in the C-terminal "tail" of p190A. This phosphorylation leads to inhibition of p190A RhoGAP activity in vitro and in vivo. These studies identify p190A as a novel GSK-3beta substrate and reveal a mechanism by which GSK-3beta contributes to cellular polarization in directionally migrating cells via effects on Rho GTPase activity.

Item Type: Article
Authors :
NameEmailORCID
Jiang, WUNSPECIFIEDUNSPECIFIED
Betson, Mm.betson@surrey.ac.ukUNSPECIFIED
Mulloy, RUNSPECIFIEDUNSPECIFIED
Foster, RUNSPECIFIEDUNSPECIFIED
Lévay, MUNSPECIFIEDUNSPECIFIED
Ligeti, EUNSPECIFIEDUNSPECIFIED
Settleman, JUNSPECIFIEDUNSPECIFIED
Date : 25 July 2008
Identification Number : https://doi.org/10.1074/jbc.M802588200
Uncontrolled Keywords : Amino Acid Sequence, Animals, Binding Sites, COS Cells, Cell Movement, Cercopithecus aethiops, DNA-Binding Proteins, Fibroblasts, GTPase-Activating Proteins, Glycogen Synthase Kinase 3, Mice, Models, Biological, Molecular Sequence Data, Mutagenesis, Site-Directed, Repressor Proteins, Sequence Homology, Amino Acid
Related URLs :
Depositing User : Symplectic Elements
Date Deposited : 17 May 2017 10:33
Last Modified : 17 May 2017 14:50
URI: http://epubs.surrey.ac.uk/id/eprint/828291

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