|
|
|
||||
| Home Help Feedback Subscriptions Archive Search Table of Contents | |||||
First published online 28 September 2004
doi: 10.1242/jcs.01410
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Research Article |

1 Department of Medical Protein Research, Flanders Interuniversity Institute for Biotechnology (V.I.B.), Ghent University, Faculty of Medicine and Health Sciences, Albert Baertsoenkaai 3, 9000 Ghent, Belgium
2 Laboratory of Experimental Cancerology, Department of Radiotherapy and Nuclear Medicine, Ghent University Hospital (1P7), De Pintelaan 185, 9000, Ghent, Belgium
Author for correspondence (e-mail: jan.gettemans{at}ugent.be)
Accepted 13 July 2004
CapG (gCap39) is a ubiquitous gelsolin-family actin modulating protein involved in cell signalling, receptor-mediated membrane ruffling, phagocytosis and motility. CapG is the only gelsolin-related actin binding protein that localizes constitutively to both nucleus and cytoplasm. Structurally related proteins like severin and fragmin are cytoplasmic because they contain a nuclear export sequence that is absent in CapG. Increased CapG expression has been reported in some cancers but a causal role for CapG in tumour development, including invasion and metastasis, has not been explored. We show that moderate expression of green fluorescent protein-tagged CapG (CapG-EGFP) in epithelial cells induces invasion into collagen type I and precultured chick heart fragments. Nuclear export sequence-tagged CapG-EGFP fails to induce invasion, whereas point mutations in the nuclear export sequence permitting nuclear re-entry restore cellular invasion. Nuclear import of CapG is energy-dependent and requires the cytosolic receptor importin ß but not importin
. Nuclear CapG does not possess intrinsic transactivation activity but suppresses VP16 transactivation of a luciferase reporter gene in a dose-dependent manner. Furthermore, invasion requires signalling through the Ras-phosphoinositide 3-kinase pathway and Cdc42 or RhoA, but not Rac1. We show for the first time active nuclear import of an actin binding protein, and our findings point to a role for nuclear CapG in eliciting invasion, possibly through interfering with the cellular transcription machinery.
Key words: CapG, gCap39, Importin, Nuclear import, Collagen, Invasion
Related articles in JCS:
This article has been cited by other articles:
![]() |
Y. Yoo, X. Wu, and J.-L. Guan A Novel Role of the Actin-nucleating Arp2/3 Complex in the Regulation of RNA Polymerase II-dependent Transcription J. Biol. Chem., March 9, 2007; 282(10): 7616 - 7623. [Abstract] [Full Text] [PDF] |
||||
![]() |
C C Thompson, F J Ashcroft, S Patel, G Saraga, D Vimalachandran, W Prime, F Campbell, A Dodson, R E Jenkins, N R Lemoine, et al. Pancreatic cancer cells overexpress gelsolin family-capping proteins, which contribute to their cell motility Gut, January 1, 2007; 56(1): 95 - 106. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Hsu, Y. Adereth, N. Kose, and V. Dammai Endocytic Function of von Hippel-Lindau Tumor Suppressor Protein Regulates Surface Localization of Fibroblast Growth Factor Receptor 1 and Cell Motility J. Biol. Chem., April 28, 2006; 281(17): 12069 - 12080. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. McDonald, G. Carrero, C. Andrin, G. de Vries, and M. J. Hendzel Nucleoplasmic {beta}-actin exists in a dynamic equilibrium between low-mobility polymeric species and rapidly diffusing populations. J. Cell Biol., February 13, 2006; 172(4): 541 - 552. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Pederson and U. Aebi Nuclear Actin Extends, with No Contraction in Sight Mol. Biol. Cell, November 1, 2005; 16(11): 5055 - 5060. [Abstract] [Full Text] [PDF] |
||||