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Cloning and expression of a Xenopus gene that prevents mitotic catastrophe in fission yeast

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Abstract

In fission yeast the Weel kinase and the functionally redundant Mikl kinase provide a regulatory mechanism to ensure that mitosis is initiated only after the completion of DNA synthesis. Yeast in which both Weel and Mik1 kinases are defective exhibit a mitotic catastrophe phenotype, presumably due to premature entry into mitosis. Because of the functional conservation of cell cycle control elements, the expression of a vertebrate weel or mikl homolog would be expected to rescue such lethal mutations in yeast. A Xenopus total ovary cDNA library was constructed in a fission yeast expression vector and used to transform a yeast temperature-dependent mitotic catastrophe mutant defective in both weel and mikl. Here we report the identification of a Xenopus cDNA clone that can rescue several different yeast mitotic catastrophe mutants defective in Weel kinase function. The expression of this clone in a weel/mikl-deficient mutant causes an elongated cell phenotype under non-permissive growth conditions. The 2.0 kb cDNA clone contains an open reading frame of 1263 nucleotides, encoding a predicted 47 kDa protein. Bacterially expressed recombinant protein was used to raise a polyclonal antibody, which specifically recognizes a 47 kDa protein from Xenopus oocyte nuclei, suggesting the gene encodes a nuclear protein in Xenopus. The ability of this cDNA to complement mitotic catastrophe mutations is independent of Weel kinase activity.

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References

  • Addison C, Jenkins J, Sturzbecher HW (1990) The p53 nuclear localization signal is structurally linked to a p34cdc2 kinase motif. Oncogene 5:423–426

    Google Scholar 

  • Amon A, Surana U, Muroff I, Nasmyth K (1992) Regulation of p34cdc28 tyrosine phosphorylation is not required for entry into mitosis in S. cerevisiae. Nature 355: 368–371

    Google Scholar 

  • Booher R, Beach D (1986) Site-specific mutagenesis of cdc2 +, a cell cycle control gene of the fission yeast Schizosaccharomyces pombe. Mol Cell Biol 6:3523–3530

    Google Scholar 

  • Booher RN, Alfa CE, Hyams JS, Beach DH (1989) The fission yeast cdc2/cdc13/sucl protein kinase: regulation of catalytic activity and nuclear localization. Cell 58:485–497

    Google Scholar 

  • Booher RN, Deshaies RJ, Kirschner MW (1993) Properties of Saccharomyces cerevisiae weel and its differential regulation of p34CDC28 in response to G1 and G2 cyclins EMBO J 12:3417–3426

    Google Scholar 

  • Brizuela L, Draetta G, Beach D (1987) p13suc1 acts in the fission yeast cell division cycle as a component of the p34cdc2 protein kinase. EMBO J 6:3507–3514

    Google Scholar 

  • Dingwall C, Laskey RA (1991) Nuclear targeting sequences—a consensus? Trends Biochem Sci 16:478–481

    Google Scholar 

  • Ducommun B, Brambilla P, Felix MA, Franza BR, Karsenti E, Draetta G (1991) cdc2 phosphorylation is required for its interaction with cyclin. EMBO J 11: 3311–3319

    Google Scholar 

  • Dunphy WG, Brizuela L, Beach D, Newport J (1988) The Xenopus cdc2 protein is a component of MPF, a cytoplasmic regulator of mitosis. Cell 54:423–431

    Google Scholar 

  • El-Deiry WS, Tokino T, Velculescu VE, Levy DB, Parsons R, Trent JM, Lin D, Mercer WE, Kinzler KW, Vogelstein B (1993) WAFT, a potential mediator of p53 tumor suppression. Cell 75: 817–825

    Google Scholar 

  • Enoch T, Nurse P (1991) Coupling M phase and S phase: controls maintaining the dependence of mitosis on chromosome replication. Cell 65:921–923

    Google Scholar 

  • Featherstone C, Russell P (1991) Fission yeast p107wee1 mitotic inhibitor is a tyrosine/scrine kinase. Nature 349: 808–811

    Google Scholar 

  • Gabrielli BG, Roy LM, Gautier J, Philippe M, Matter JL (1992) A cdc2-related kinase oscillates in the cell cycle independently of G2/M cyclins and cdc2. J Biol Chem 267:1969–1975

    Google Scholar 

  • Gautier J, Norbury C, Lohka M, Nurse P, Matter J (1988) Purified maturation-promoting factor contains the product of a Xenopus homolog of the fission yeast cell cycle control gene cdc2+. Cell 54:433–439

    Google Scholar 

  • Gautier J, Solomon MJ, Booher RN, Bazan JF, Kirschner MW (1991) cdc25 is a specific tyrosine phosphotase that directly activates p34cdc2. Cell 67:197–211

    Google Scholar 

  • Gould KL, Nurse P (1989) Tyrosine phosphorylation of the fission yeast cdc2 + protein kinase regulates entry into mitosis. Nature 342:39–45

    Google Scholar 

  • Gould KL, Moreno S, Owen DJ, Sazer S, Nurse P (1991) Phosphorylation at Thr167 is required for fission yeast p 34cdc2 function. EMBO J 10:3297–3309

    Google Scholar 

  • Gu Y, Turck CW, Morgan DO (1993) Inhibition of CDK2 activity in vivo by an associated 20k regulatory subunit. Nature 366:707–710

    Google Scholar 

  • Hagan IM, Hayles J, Nurse P (1988) Cloning and sequencing of the cyclin-related cdc13 + gene and a cytological study of its role in fission yeast mitosis. J Cell Sci 91: 587–595

    Google Scholar 

  • Harlow E, Lane D (1988) Antibodies: a laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York

    Google Scholar 

  • Igarashi M, Nagata A, Jinno S, Suto K, Okayama H (1991) Wee1+-like gene in human cells. Nature 353: 80–83

    Google Scholar 

  • Kemp BE, Pearson RB (1990) Protein kinase recognition sequence motifs. Trends Biochem Sci 15:342–346

    Google Scholar 

  • Kumagai A, Dunphy WG (1991) The cdc25 protein controls tyrosine dephosphorylation of the cdc2 protein in a cell-free system. Cell 64:903–914

    Google Scholar 

  • Lee MS, Ogg S, Xu M, Parker LL, Donoghue DL, Maller JL, Piwnica-Worms H (1992) cdc25 + encodes a protein phosphatase that dephosphorylates p34cdc. Mol Biol Cell 3:73–84

    Google Scholar 

  • Lohka MJ, Hayes MK, Matter JL (1988) Purification of maturation-promoting factor, an intracellular regulator of early mitotic events. Proc Natl Acad Sci USA 85:3009–3013

    Google Scholar 

  • Lundgren K, Walworth N, Booher R, Dembski M, Kirschner M, Beach D (1991) mikl and weel cooperate in the inhibitory tyrosine phosphorylation of cdc2. Cell 64:1111–1122

    Google Scholar 

  • Matter JL (1994) Biochemistry of cell cycle checkpoints at the G2/M and metaphase/anaphase transitions. Semin Dev Biol 5: 3061–3068

    Google Scholar 

  • Maundrell K (1993) Thiamine-repressible expression vectors pREP and pRIP for fission yeast. Gene 123:127–130

    Google Scholar 

  • McLeod M, Stein M, Beach D (1987) The product of the mei3 + gene, expressed under control of the mating-type locus, induces meiosis and sporulation in fission yeast. EMBO J 6:729–736

    Google Scholar 

  • Millar JBA, McGowan CH, Lenaers G, Jones R, Russell P (1991) p80cdc25 mitotic inducer is the tyrosine phosphatase that activates p34cdc2 kinase in fission yeast. EMBO J 10:4301–4309

    Google Scholar 

  • Molz L, Beach D (1993) Characterization of the fission yeast mcs2 cyclin and its associated protein kinase activity. EMBO J 12:1723–1732

    Google Scholar 

  • Molz L, Booher R, Young P, Beach D (1989) cdc2 and the regulation of mitosis: six interacting mcs genes: Genetics 122:773–782

    Google Scholar 

  • Moreno S, Hayles J, Nurse P (1989) Regulation of p34cdc2 protein kinase during mitosis. Cell 58: 361–372

    Google Scholar 

  • Moreno S, Nurse P, Russell P (1990) Regulation of mitosis by cyclic accumulation of p80cdc25 mitotic inducer in fission yeast. Nature 344:549–552

    Google Scholar 

  • Moreno S, Klar A, Nurse P (1991) Molecular genetic analysis of fission yeast, Schizosaccharomyces pombe. Methods Enzymol 194:795–823

    Google Scholar 

  • Murray A (1989) The cell cycle as a cdc2 cycle. Nature 342:14–15

    Google Scholar 

  • Murray A (1992) Creative blocks: cell-cycle checkpoints and feedback control. Nature 359: 599–604

    Article  CAS  PubMed  Google Scholar 

  • Murray A, Hunt T (1993) The cell cycle: an introduction. W.H. Freeman and Company, New York.

    Google Scholar 

  • Nurse P (1975) Genetic control of cell size at cell division in yeast. Nature 256:547–551

    Google Scholar 

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

    Google Scholar 

  • Parker LL, Atherton-Fessler S, Piwnica-Worms H (1992) p107wee1 is a dual-specificity kinase that phosphorylates p34cdc2 on tyrosine 15. Proc Natl Acad Sci USA 89:2917–2921

    Google Scholar 

  • Pines J, Hunter T (1990) p34cdc2: the S and M kinase. New Biol 2:389–401

    Google Scholar 

  • Robbins J, Dilworth SM, Laskey RA, Dingwall C (1991) Two interdependent basic domains in nucleoplasmin nuclear targeting sequence: identification of a class of bipartite nuclear targeting sequence. Cell 64:615–623

    Google Scholar 

  • Russell P (1983) Evolutionary divergence of the mRNA transcription initiation mechanism in yeast. Nature 301:167–169

    Google Scholar 

  • Russell P, Hall BD (1983) The primary structure of the alcohol dehydrogenase gene from the fission yeast Schizosaccharomyces pombe. J Biol Chem 258:143–149

    Google Scholar 

  • Russell P, Nurse P (1986) cdc25 + functions as a mitotic inducer in fission yeast. Cell 45:145–153

    Google Scholar 

  • Russell P, Nurse P (1987) Negative regulation of mitosis by weel +, a gene encoding a protein kinase homolog. Cell 49:559–567

    Google Scholar 

  • Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York

    Google Scholar 

  • Serrano M, Hannon GJ, Beach D (1993) A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4. Nature 366:704–707

    Google Scholar 

  • Simanis V, Nurse P (1986) The cell cycle control gene cdc2 + of fission yeast encodes a protein kinase potentially regulated by phosphorylation. Cell 45:261–268

    Google Scholar 

  • Sorger PK, Murray AW (1992) S-phase feedback control in budding yeast independent of tyrosine phosphorylation of p34cdc28. Nature 355:365–368

    Google Scholar 

  • Strausfeld U, Labbe JC, Fesquet D, Cavadore JC, Picard A, Sadhu K, Russell P, Doree M (1991) Dephosphorylation and activation of a p34cdc2/cyclin B complex in vitro by human CDC25 protein. Nature 351:242–245

    Google Scholar 

  • Su JY, Maller JL (1994) Identification of a Xenopus cDNA that prevents mitotic catastrophe in the fission yeast Schizosaccharomyces pombe. Gene 145:155–156

    Google Scholar 

  • Xiong Y, Hannon GJ, Zhang H, Casso D, Kobayashi R, Beach D (1993) p21 is a universal inhibitor of cyclin kinases. Nature 366:701–704

    Google Scholar 

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Communicated by B. Kilbey

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Su, JY., Maller, J.L. Cloning and expression of a Xenopus gene that prevents mitotic catastrophe in fission yeast. Molec. Gen. Genet. 246, 387–396 (1995). https://doi.org/10.1007/BF00288613

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  • DOI: https://doi.org/10.1007/BF00288613

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