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Wee1+-like gene in human cells

Abstract

THE wee1+ gene is a mitotic inhibitor controlling the G2 to M transition of the fission yeast Schizosaccharomyces pombe1 and encodes a protein kinase with both serine- and tyrosine-phosphorylating activities2. We have cloned a human gene (WEElHu) similar to weel+ by transcomplementation of a yeast mutant3,4. WEElHu encodes a protein homologous to the S. pombe weel+ and mik1+ (a functionally redundant sibling of weel+)5 kinases and effectively rescues a wee1 mutation. We report here that overexpression of WEE1Hu in fission yeast generates very elongated cells as a result of inhibition of the G2-M transition in the cell cycle. In addition, we detected a 3-kilobase-long WEE1Hu messenger RNA in all the human cell lines we examined. We conclude that a wee1+-like gene exists and is expressed in human cells.

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References

  1. Russell, P. & Nurse, P. Cell 49, 559–567 (1987).

    Article  CAS  Google Scholar 

  2. Featherstone, C. & Russell, P. Nature 349, 808–811 (1991).

    Article  ADS  CAS  Google Scholar 

  3. Lee, M. & Nurse, P. Nature 327, 31–35 (1987).

    Article  ADS  CAS  Google Scholar 

  4. Okazaki, K., Okazaki, N., Kume, K., Jinno, S. & Okayama, H. Nucleic Acids Res. 18, 6485–6489 (1990).

    Article  CAS  Google Scholar 

  5. Lundgren, K. et al. Cell 64, 1111–1122 (1991).

    Article  CAS  Google Scholar 

  6. Russell, P. & Nurse, P. Cell 45, 145–153 (1986).

    Article  CAS  Google Scholar 

  7. Chen, C. & Okayama, H. Molec. cell. Biol. 7, 2745–2752 (1987).

    Article  CAS  Google Scholar 

  8. Hanks, S. K., Quinn, A. M. & Hunter, T. Science 241, 24–52 (1988).

    Article  Google Scholar 

  9. Toyama, R. & Okayama, H. FEBS Lett. 268, 217–221 (1990).

    Article  CAS  Google Scholar 

  10. Edgar, B. A. & O'Farrell, P. H. Cell 57, 177–187 (1989).

    Article  CAS  Google Scholar 

  11. Sadhu, K., Reed, S. I., Richardson, H. & Russell, P. Proc. natn. Acad. Sci. U.S.A. 87, 5139–5143 (1990).

    Article  ADS  CAS  Google Scholar 

  12. Kumagai, A. & Dunphy, W. G. Cell 64, 903–914 (1991).

    Article  CAS  Google Scholar 

  13. Gutz, H., Heslot, H., Leupold, U. & Loprieno, N. In Handbook of Genetics Vol. 1 (ed. King, R. D.) 395–446 (Plenum, New York, 1974).

    Google Scholar 

  14. Rothstein, R. in DNA Cloning—A Practical Approach Vol. 2 (ed. Glover, D. M.) 45–65 (IRL, Oxford, 1985).

    Google Scholar 

  15. Inoue, H., Nojima, H. & Okayama, H. Gene 96, 23–28 (1990).

    Article  CAS  Google Scholar 

  16. Sanger, F., Nicklen, S., Barrell, B. G., Smith, A. J. H. & Roe, B. A. Proc. natn. Acad. Sci. U.S.A. 74, 5463–5467 (1977).

    Article  ADS  CAS  Google Scholar 

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Igarashi, M., Nagata, A., Jinno, S. et al. Wee1+-like gene in human cells. Nature 353, 80–83 (1991). https://doi.org/10.1038/353080a0

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