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MARCKS is an actin filament crosslinking protein regulated by protein kinase C and calcium–calmodulin

Abstract

AGONISTS that stimulate protein kinase C (PKC) induce profound changes in cell morphology correlating with the reorganization of submembranous actin1,2, but no direct connection between PKC and actin assembly has been identified3. The myristoylated, alanine-rich C kinase substrate (MARCKS) binds calmodulin4,5 and is a predominant, specific substrate of PKC which is phosphorylated during macrophage and neutrophil activation6–8, growth factor-dependent mitogenesis9,10and neurosecretion11,12; it is redistributed from plasma membrane to cytoplasm when phosphorylated13–15 and is involved in leukocyte motility14,15. Here we report that MARCKS is a filamentous (F) actin crosslinking protein, with activity that is inhibited by PKC-mediated phosphorylation and by binding to calcium–calmodulin. MARCKS may be a regulated crossbridge between actin and the plasma membrane, and modulation of the actin crosslinking activity of the MARCKS protein by calmodulin and phosphorylation represents a potential convergence of the calcium–calmodulin and PKC signal transduction pathways in the regulation of the actin cytoskeleton.

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References

  1. Phaire-Washington, L., Silverstein, S. C. & Wang, E. J. Cell Biol. 86, 641–655 (1980).

    Article  CAS  PubMed  Google Scholar 

  2. Sheterline, P., Rickard, J., Boothroyd, B. & Richards, R. J. Muscle Res. Cell Motil. 7, 405–412 (1986).

    Article  CAS  PubMed  Google Scholar 

  3. Stossel, T. P. J. biol. Chem. 264, 18261–18264 (1989).

    CAS  PubMed  Google Scholar 

  4. Graff, J. M., Young, T. M., Johnson, J. D. & Blackshear, P. J. J. biol. Chem. 264, 21818–21823 (1989).

    CAS  PubMed  Google Scholar 

  5. Mcllroy, B. K., Walters, J. D., Blackshear, P. J. & Johnson, J. D. J. biol. Chem. 266, 4959–4964 (1991).

    Google Scholar 

  6. Aderem, A. A. et al. Nature 332, 362–364 (1988).

    Article  ADS  CAS  PubMed  Google Scholar 

  7. Rosen, A., Nairn, A. C., Greengard, P., Cohn, Z. A. & Aderem, A. A. J. biol. Chem. 264, 9118–9121 (1989).

    CAS  PubMed  Google Scholar 

  8. Thelen, M., Rosen, A., Nairn, A. C. & Aderem, A. Proc. natn. Acad. Sci. U.S.A. 87, 5603–5607 (1990).

    Article  ADS  CAS  Google Scholar 

  9. Blackshear, P. J., Wen, L., Glynn, B. P. & Witters, L. A. J. biol. Chem. 261, 1459–1469 (1986).

    CAS  PubMed  Google Scholar 

  10. Rozengurt, E., Rodriguez-Pena, M. & Smith, K. A. Proc. natn. Acad. Sci. U.S.A 80, 7244–7248 (1983).

    Article  ADS  CAS  Google Scholar 

  11. Wu, W. S., Walaas, S. I., Nairn, A. C. & Greengard, P. Proc. natn. Acad. Sci. U.S.A. 79, 5249–5253 (1982).

    Article  ADS  CAS  Google Scholar 

  12. Kligman, D. & Patel, J. J. Neurochem. 47, 298–303 (1986).

    Article  CAS  PubMed  Google Scholar 

  13. Wang, J. K. T., Walaas, S. I., Sihra, T. S., Aderem, A. A. & Greengard, P. Proc. natn. Acad. Sci. U.S.A. 86, 2253–2256 (1989).

    Article  ADS  CAS  Google Scholar 

  14. Rosen, A., Keenan, K. F., Thelen, M., Nairn, A. C. & Aderem, A. A. J. exp. Med. 172, 1211–1215 (1990).

    Article  CAS  PubMed  Google Scholar 

  15. Thelen, M., Rosen, A., Nairn, A. C. & Aderem, A. Nature 351, 320–322 (1991).

    Article  ADS  CAS  PubMed  Google Scholar 

  16. Heuser, J. J. molec. Biol. 169, 155–195 (1983).

    Article  CAS  PubMed  Google Scholar 

  17. Albert, K. A., Nairn, A. C. & Greengard, P. Proc. natn. Acad. Sci. U.S.A. 84, 7046–7050 (1987).

    Article  ADS  CAS  Google Scholar 

  18. Stumpo, D. J., Graff, J. M., Albert, K. A., Greengard, P. & Blackshear, P. J. Proc. natn. Acad. Sci. U.S.A. 86, 4012–4016 (1989).

    Article  ADS  CAS  Google Scholar 

  19. Graff, J. M., Stumpo, D. J. & Blackshear, P. J Molec. Endocr. 3, 1903–1906 (1989).

    Article  CAS  PubMed  Google Scholar 

  20. Seykora, J. T., Ravetch, J. V. & Aderem, A. Proc. natn. Acad. Sci. U.S.A. 88, 2505–2509 (1991).

    Article  ADS  CAS  Google Scholar 

  21. Corwin, H. L. & Hartwig, J. H. Devl Biol. 99, 61–74 (1983).

    Article  CAS  Google Scholar 

  22. Wegner, A. J. molec. Biol. 108, 139–150 (1976).

    Article  CAS  PubMed  Google Scholar 

  23. Albert, K. A., Wu, W. S., Nairn, A. C. & Greengard, P. Proc. natn. Acad. Sci. U.S.A. 81, 3622–3625 (1984).

    Article  ADS  CAS  Google Scholar 

  24. Graff, J. M., Stumpo, D. J. & Blackshear, P. J. J. biol. Chem. 264, 11912–11919 (1989).

    CAS  PubMed  Google Scholar 

  25. O'Neil, K. T. & Degrado, W. F. Trends Biochem. Sci. 15, 59–64 (1990).

    Article  CAS  PubMed  Google Scholar 

  26. Vandekerckhove, J. Curr. Opinion Cell Biol. 1, 15–22 (1989).

    Article  CAS  PubMed  Google Scholar 

  27. Snyderman, R. & Verghese, M. W. Rev. Infect. Dis. 9, 562–569 (1987).

    Article  Google Scholar 

  28. Spudich, J. A. & Watt, S. J. biol. Chem. 246, 4866–4871 (1971).

    CAS  PubMed  Google Scholar 

  29. Mac Lean-Fletcher, S. D. & Pollard, T. D. J. Cell Biol. 85, 414–428 (1980).

    Article  CAS  Google Scholar 

  30. Yin, H. L., Zaner, K. S. & Stossel, T. P. J. biol. Chem. 255, 9494–9500 (1980)

    CAS  PubMed  Google Scholar 

  31. Berne, B. & Pecora, R. Dynamic Light Scattering (Wiley, New York, 1976).

    Google Scholar 

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Hartwig, J., Thelen, M., Resen, A. et al. MARCKS is an actin filament crosslinking protein regulated by protein kinase C and calcium–calmodulin. Nature 356, 618–622 (1992). https://doi.org/10.1038/356618a0

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