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.

  • Letter
  • Published:

Role of calcineurin and Mpk1 in regulating the onset of mitosis in budding yeast

Abstract

Signalling via calcium is probably involved in regulating eukaryotic cell proliferation, but details of its mechanism of action are unknown1,2. In Schizosaccharomyces pombe, the onset of mitosis is determined by activation of a complex of the p34cdc2 protein kinase and a cyclin protein that is specific to the G2 phase of the cell cycle. This activation requires dephosphorylation of p34cdc2 (ref. 3). Wee1, a tyrosine kinase that inhibits p34cdc2 by phosphorylating it, is needed to determine the length of G2 phase. Here we show that calcium-activated pathways in Saccharomyces cerevisiae control the onset of mitosis by regulating Swe1, a Wee1 homologue. Zds1 (also known as Oss1 and Hst1) (47) is important in repressing the transcription of SWE1 in G2 phase. In the presence of high calcium levels, cells lacking Zds1 are delayed in entering mitosis. Calcineurin8,9,10,11 and Mpk1 (refs 12, 13) regulate Swe1 activation at the transcriptional and post-translational levels, respectively, and both are required for the calcium-induced delay in G2 phase. These cellular pathways also induce a G2-phase delay in response to hypotonic shock.

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: Ca2+-induced G2 delay in the Δzds1 strain and its suppression by deletion of SWE1, CNB1 and MPK1.
Figure 2: The G2 delay induced by overproduction of a constitutively active form of calcineurin (Cmp2ΔC) or Mpk1 in Δzds1 and Δzds1 Δswe1 cells.
Figure 3: Ca2+-induced activation of transcription of SWE1 in G2.
Figure 4: Hsl1-mediated regulation of Swe1 by Mpk1.
Figure 5: A model of the Ca2+-mediated G2-phase delay in budding yeast.
Figure 6: Hypotonic-shock-induced G2 delay.

Similar content being viewed by others

References

  1. Means, A. R. Calcium, calmodulin and cell cycle regulation. FEBS Lett. 347, 1–4 (1994).

    Article  ADS  CAS  Google Scholar 

  2. Clapham, D. E. Calcium signaling. Cell 80, 259–268 (1995).

    Article  CAS  Google Scholar 

  3. Nurse, P. Universal control mechanism regulating onset of M-phase. Nature 344, 503–507 (1990).

    Article  ADS  CAS  Google Scholar 

  4. Tsuchiya, E.et al. The Saccharomyces cerevisiae SSD1 gene is involved in the tolerance to high concentration of Ca2+ with the participation of HST1/NRC1/BFR1. Gene 176, 35–38 (1996).

    Article  CAS  Google Scholar 

  5. Ma, X.-J., Lu, Q. & Grunstein, M. Asearch for proteins that interact genetically with histone H3 and H4 amino termini uncovers novel regulators of the SWE1 kinase in Saccharomyces cerevisiae. Genes Dev. 10, 1327–1340 (1996).

    Article  CAS  Google Scholar 

  6. Yu, Y.et al. Mutation in the homologous ZDS1 and ZDS2 genes affect cell cycle progression. Mol. Cell Biol. 16, 5254–5263 (1996).

    Article  CAS  Google Scholar 

  7. Bi, E. & Pringle, J. R. ZDS1 and ZDS2, genes whose products may regulate Cdc42p in Saccharomyces cerevisiae. Mol. Cell Biol. 16, 5264–5275 (1996).

    Article  CAS  Google Scholar 

  8. Liu, Y.et al. The Saccharomyces cerevisiae genes (CMP1 and CMP2) encoding calmodulin-binding proteins homologous to the catalytic subunit of mammalian protein phosphatase 2B. Mol. Gen. Genet. 227, 52–59 (1991).

    Article  CAS  Google Scholar 

  9. Kuno, T.et al. cDNA cloning of a calcineurin B homolog in Saccharomyces cerevisiae. Biochem. Biophys. Res. Commun. 180, 1159–1163 (1991).

    Article  CAS  Google Scholar 

  10. Cyert, M. S., Kunisawa, R., Kaim, D. & Thorner, J. Yeast has homologs (CNA1 and CNA2 gene products) of mammalian calcineurin, a calmodulin-regulated phosphoprotein phosphatase. Proc. Natl Acad. Sci. USA 88, 7376–7380 (1991).

    Article  ADS  CAS  Google Scholar 

  11. Cyert, M. S. & Thorner, J. Regulatory subunit (CNB1 gene product) of yeast Ca2+/calmodulin-dependent protein phosphatase is required for adaptation to pheromone. Mol. Cell Biol. 12, 3460–3469 (1992).

    Article  CAS  Google Scholar 

  12. Errede, B. & Levin, D. E. Aconserved kinase cascade for MAP kinase activation in yeast. Curr. Opin. Cell Biol. 5, 254–260 (1993).

    Article  CAS  Google Scholar 

  13. Levin, D. E. & Errede, B. The proliferation of MAP kinase signalling pathways in yeast. Curr. Opin. Cell Biol. 7, 197–202 (1995).

    Article  CAS  Google Scholar 

  14. Booher, R. N., Deshaies, R. J. & Kirschner, M. W. Properties of Saccharomyces cerevisiae wee1 and its diffential regulation of p34CDC28 in response to G1 and G2 cyclins. EMBO J. 12, 3417–3426 (1993).

    Article  CAS  Google Scholar 

  15. Foor, F.et al. Calcineurin mediates inhibition by FK506 and cyclosporin of recovery from α-factor arrest in yeast. Nature 360, 682–684 (1992).

    Article  ADS  CAS  Google Scholar 

  16. Nakamura, T.et al. Protein phosphatase type 2B (calcineurin)-mediated, FK506-sensitive regulation of intracellular ions in yeast is an important determinant for adaptation to high salt stress conditions. EMBO J. 12, 4063–4071 (1993).

    Article  CAS  Google Scholar 

  17. Nakamura, T., Ohmoto, T., Hirata, D., Tsuchiya, E. & Miyakawa, T. Genetic evidence for the functional redundancy of the calcineurin- and Mpk1-mediated pathways in the regulation of cellular events important for growth in Saccharomyces cerevisiae. Mol. Gen. Genet. 251, 211–219 (1996).

    CAS  PubMed  Google Scholar 

  18. Tanaka, S. & Nojima, H. Nik1: a Nim1-like protein kinase of S. cerevisiae interacts with the Cdc28 complex and regulates cell cycle progression. Genes to Cells 1, 905–921 (1996).

    Article  CAS  Google Scholar 

  19. Mazur, C.et al. Differential expression and function of two homologous subunits of yeast 1, 3-β-D-glucan synthase. Mol. Cell Biol. 15, 5671–5681 (1995).

    Article  CAS  Google Scholar 

  20. Kamada, Y., Jung, U. S., Piotrowski, J. & Levin, D. E. The protein kinase C-activated MAP kinase pathway of Saccharomyces cerevisiae mediates a novel aspect of the heat shock response. Genes Dev. 9, 1559–1571 (1995).

    Article  CAS  Google Scholar 

  21. Batiza, A. F., Schulz, T. & Masson, P. H. Yeast respond to hypotonic shock with a calcium pulse. J. Biol. Chem. 271, 23357–23362 (1996).

    Article  CAS  Google Scholar 

  22. Davenport, K. R., Sohaskey, M., Kamada, Y., Levin, D. E. & Gustin, M. C. Asecond osmosensing signal transduction pathway in yeast. J. Biol. Chem. 270, 30157–30161 (1995).

    Article  CAS  Google Scholar 

  23. Martinac, B., Adler, J. & Kung, C. Mechanosensitive ion channels of E. coli activated by amphipaths. Nature 348, 261–263 (1990).

    Article  ADS  CAS  Google Scholar 

  24. Igual, J. C., Johnson, A. L. & Johnston, L. H. Coordinated regulationof gene expression by the cell cycle transcription factor SW14 and the protein kinase C MAP kinase pathway for yeast cell integrity. EMBO J. 15, 5001–5013 (1996).

    Article  CAS  Google Scholar 

  25. Zarzov, P., Mazzoni, C. & Mann, C. The SLT2 (MPK1) MAP kinase is activated during periods of polarized cell growth in yeast. EMBO J. 15, 81–91 (1996).

    Article  Google Scholar 

Download references

Acknowledgements

We thank M. Grunstein for the HSL1 disruption plasmid, D. E. Levin for the plasmid containing the gene for HA-tagged Mpk1, and K. Matsumoto and Y. Ohya for discussions.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Tokichi Miyakawa.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mizunuma, M., Hirata, D., Miyahara, K. et al. Role of calcineurin and Mpk1 in regulating the onset of mitosis in budding yeast. Nature 392, 303–306 (1998). https://doi.org/10.1038/32695

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/32695

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing