Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Original Paper
  • Published:

Cooperation of Cdc42 small G protein-activating and actin filament-binding activities of frabin in microspike formation

Abstract

Frabin is a GDP/GTP exchange protein for Cdc42 with actin filament (F-actin)-binding activity. Cdc42 is a small GTP-binding protein that forms filopodia-like microspikes in a variety of cells. Expression of frabin indeed forms microspikes through at least activation of Cdc42 in MDCK cells and fibroblasts such as COS7, L, and NIH3T3 cells. However, the role of the F-actin-binding activity of frabin in the microspike formation remains unknown. We have examined here this role of frabin by expressing various frabin mutants, which have lost Cdc42-activating or F-actin-binding activity, with or without a dominant active mutant of Cdc42 in MDCK and COS7 cells. We show here that for the microspike formation, either of the Cdc42-activating and F- actin-binding activities of frabin alone is not sufficient and both the activities are necessary and that both the activities play a cooperative role in the microspike formation. The present results, together with the earlier finding that Cdc42 reorganizes the actin cytoskeleton at least through the N-WASP-Arp2/3 complex, suggest that frabin directly and indirectly reorganizes the actin cytoskeleton through its F-actin-binding and Cdc42-activating activities, respectively, in a cooperative manner, eventually leading to microspike formation.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1
Figure 2
Figure 3
Figure 4
Figure 5

Similar content being viewed by others

References

  • Bellanger J-M, Astier C, Sardet C, Ohta Y, Stossel TP, Debant A . 2000 Nature Cell Biol. 2: 888–892

  • Bourguignon LY, Zhu H, Shao L, Chen YW . 2000 J. Cell Biol. 150: 177–191

  • Bradford MM . 1976 Anal. Biochem. 72: 248–254

  • Debant A, Serra-Pages C, Seipel K, O'Brien S, Tang M, Park SH, Streuli M . 1996 Natl. Acad. Sci. USA 93: 5466–5471

  • Gorski JL, Estrada L, Hu C, Liu Z . 2000 Developmental Dynamics 218: 573–586

  • Hall A . 1998 Science 279: 509–514

  • Hordijk PL, ten Klooster JP, van der Kammen RA, Michiels F, Oomen LC, Collard JG . 1997 Science 278: 1464–1466

  • Jou TS, Nelson WJ . 1998 J. Cell Biol. 142: 85–100

  • Kodama A, Takaishi K, Nakano K, Nishioka H, Takai Y . 1999 Oncogene 18: 3996–4006

  • Laemmli UK . 1970 Nature 227: 680–685

  • Mandai K, Nakanishi H, Satoh A, Obaishi H, Wada M, Nishioka H, Itoh M, Mizoguchi A, Aoki T, Fujimoto T, Matsuda Y, Tsukita S, Takai Y . 1997 J. Cell Biol. 139: 517–528

  • Michiels F, Habets GG, Stam JC, van der Kammen RA, Collard JG . 1995 Nature 375: 338–340

  • Miki H, Sasaki T, Takai Y, Takenawa T . 1998 Nature 391: 93–96

  • Mizushima S, Nagata S . 1990 Nucleic Acids Res. 18: 5322

  • Obaishi H, Nakanishi H, Mandai K, Satoh K, Satoh A, Takahashi K, Miyahara M, Nishioka H, Takaishi K, Takai Y . 1998 J. Biol. Chem. 273: 18697–18700

  • Ono Y, Nakanishi H, Nishimura M, Kakizaki M, Takahashi K, Miyahara M, Satoh-Horikawa K, Mandai K, Takai Y . 2000 Oncogene 19: 3050–3058

  • Pardee JD, Spudich JA . 1982 Methods Enzymol. 85: 164–181

  • Pasteris NG, Cadle A, Logie LJ, Porteous MEM, Schwartz CE, Stevenson RE, Glover TW, Wilroy RS, Gorski JL . 1994 Cell 79: 669–678

  • Pasteris NG, Gorski JL . 1999 Genomics 60: 57–66

  • Pasteris NG, Nagata K, Hall A, Gorski JL . 2000 Gene 242: 237–247

  • Rohatgi R, Ma L, Miki H, Lopez M, Kirchhausen T, Takenawa T, Kirschner NW . 1999 Cell 97: 221–231

  • Takahashi K, Nakanishi H, Miyahara M, Mandai K, Satoh K, Satoh A, Nishioka H, Aoki J, Nomoto A, Mizoguchi A, Takai Y . 1999 J. Cell Biol. 145: 539–549

  • Takai Y, Sasaki T, Matozaki T . 2000 Physiol. Rev. 81: 153–208

  • Takaishi K, Sasaki T, Kotani H, Nishioka H, Takai Y . 1997 J. Cell Biol. 139: 1047–1059

  • Umikawa M, Obaishi H, Nakanishi H, Satoh-Horikawa K, Takahashi K, Hotta I, Matsuura Y, Takai Y . 1999 J. Biol. Chem. 274: 25197–25200

  • Yasuda T, Ohtsuka T, Inoue E, Yokoyama S, Sakisaka T, Kodama A, Takaishi K, Takai Y . 2000 Genes Cells 5: 583–591

Download references

Acknowledgements

This work was supported by grants-in-aid for Scientific Research and for Cancer Research from the Ministry of Education, Science, Sports and Culture, Japan (2000).

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ikeda, W., Nakanishi, H., Tanaka, Y. et al. Cooperation of Cdc42 small G protein-activating and actin filament-binding activities of frabin in microspike formation. Oncogene 20, 3457–3463 (2001). https://doi.org/10.1038/sj.onc.1204463

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/sj.onc.1204463

Keywords

This article is cited by

Search

Quick links