A dominant negative allele of p34cdc2 shows altered phosphoamino acid content and sequesters p56cdc13 cyclin

The cdc2 gene product, a 34-kDa phosphoprotein with serine/threonine protein kinase activity, has been implicated as the key component in the regulation of the eucaryotic cell cycle. Activation of the cdc2 protein kinase is regulated by its phosphorylation state and by interaction with other proteins. We have mutagenized the fission yeast cdc2 gene to obtain conditionally dominant negative alleles. One of these mutants, named DL2, is characterized in this report. Overexpression of the mutant protein in a wild-type cdc2 background is lethal and leads to arrest in the G2 phase of the cell cycle. The mutant phenotype is the result of a single amino acid change in the GDSEID motif of the protein, a region of identity in all cdc2 homologs, and results in a nonfunctional protein that shows an altered content of phosphothreonine. Multicopy suppressors of the dominant negative phenotype have been isolated, and one of these has been shown to encode the cdc13 cyclin B gene product.

[1]  B. Sefton,et al.  Acid and base hydrolysis of phosphoproteins bound to immobilon facilitates analysis of phosphoamino acids in gel-fractionated proteins. , 1989, Analytical biochemistry.

[2]  Karen Lundgren,et al.  mik1 and wee1 cooperate in the inhibitory tyrosine phosphorylation of cdc2 , 1991, Cell.

[3]  Paul Russell,et al.  cdc25 + functions as an inducer in the mitotic control of fission yeast , 1986, Cell.

[4]  Jean Gautier,et al.  Purified maturation-promoting factor contains the product of a Xenopus homolog of the fission yeast cell cycle control gene cdc2 + , 1988, Cell.

[5]  S. Reed,et al.  Mitotic role for the Cdc28 protein kinase of Saccharomyces cerevisiae. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[6]  H. Hirt,et al.  Complementation of a yeast cell cycle mutant by an alfalfa cDNA encoding a protein kinase homologous to p34cdc2. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[7]  J. Hindley,et al.  Sequence of the cell division gene CDC2 from Schizosaccharomyces pombe; patterns of splicing and homology to protein kinases. , 1984, Gene.

[8]  Sergio Moreno,et al.  Regulation of p34cdc2 protein kinase during mitosis , 1989, Cell.

[9]  Paul Russell,et al.  Negative regulation of mitosis by wee1 +, a gene encoding a protein kinase homolog , 1987, Cell.

[10]  D. Beach,et al.  Reversible tyrosine phosphorylation of cdc2: Dephosphorylation accompanies activation during entry into mitosis , 1989, Cell.

[11]  Kathleen L. Gould,et al.  Tyrosine phosphorylation of the fission yeast cdc2+ protein kinase regulates entry into mitosis , 1989, Nature.

[12]  K. Gould,et al.  Phosphorylation at Thr167 is required for Schizosaccharomyces pombe p34cdc2 function. , 1991, The EMBO journal.

[13]  P. Fantes Epistatic gene interactions in the control of division in fission yeast , 1979, Nature.

[14]  D. Beach,et al.  The Xenopus cdc2 protein is a component of MPF, a cytoplasmic regulator of mitosis , 1988, Cell.

[15]  P. Nurse,et al.  Complementation used to clone a human homologue of the fission yeast cell cycle control gene cdc2 , 1987, Nature.

[16]  N. Spurr,et al.  Cloning of the mouse homologue of the yeast cell cycle control gene cdc2. , 1990, DNA sequence : the journal of DNA sequencing and mapping.

[17]  J. Corden,et al.  Phosphorylation of RNA polymerase by the murine homologue of the cell-cycle control protein cdc2 , 1989, Nature.

[18]  E. Nigg,et al.  Structure and developmental expression of the chicken CDC2 kinase. , 1989, The EMBO journal.

[19]  J. Maller,et al.  Cyclin B in Xenopus oocytes: implications for the mechanism of pre‐MPF activation. , 1991, The EMBO journal.

[20]  P. Nurse Universal control mechanism regulating onset of M-phase , 1990, Nature.

[21]  M. Dasso,et al.  Completion of DNA replication is monitored by a feedback system that controls the initiation of mitosis in vitro: Studies in Xenopus , 1990, Cell.

[22]  Tony Hunter,et al.  Isolation of a human cyclin cDNA: Evidence for cyclin mRNA and protein regulation in the cell cycle and for interaction with p34cdc2 , 1989, Cell.

[23]  A. Kumagai,et al.  The cdc25 protein contains an intrinsic phosphatase activity , 1991, Cell.

[24]  Jean,et al.  Cyclin B targets p34cdc2 for tyrosine phosphorylation. , 1991, The EMBO journal.

[25]  J. Newport,et al.  Fission yeast p13 blocks mitotic activation and tyrosine dephosphorylation of the Xenopus cdc2 protein kinase , 1989, Cell.

[26]  Marc W. Kirschner,et al.  cdc25 is a specific tyrosine phosphatase that directly activates p34cdc2 , 1991, Cell.

[27]  D. Marshak,et al.  Cell cycle control of DNA replication by a homologue from human cells of the p34cdc2 protein kinase. , 1990, Science.

[28]  D. Morrison,et al.  Human cdc2 protein kinase is a major cell-cycle regulated tyrosine kinase substrate , 1988, Nature.

[29]  J. Maller,et al.  Dephosphorylation and activation of Xenopusp34cdc2 protein kinase during the cell cycle , 1989, Nature.

[30]  B. Franza,et al.  cdc2 phosphorylation is required for its interaction with cyclin. , 1991, The EMBO journal.

[31]  K. Maundrell nmt1 of fission yeast. A highly transcribed gene completely repressed by thiamine. , 1990, The Journal of biological chemistry.

[32]  Sergio Moreno,et al.  Regulation of mitosis by cyclic accumulation of p80cdc25 mitotic inducer in fission yeast , 1990, Nature.

[33]  S. Sherwood,et al.  Mitochondrial growth and DNA synthesis occur in the absence of nuclear DNA replication in fission yeast. , 1990, Journal of cell science.

[34]  Margaret S. Lee,et al.  Cyclin promotes the tyrosine phosphorylation of p34cdc2 in a wee1+ dependent manner. , 1991, The EMBO journal.

[35]  E. Nigg,et al.  Differential phosphorylation of vertebrate p34cdc2 kinase at the G1/S and G2/M transitions of the cell cycle: identification of major phosphorylation sites. , 1991, The EMBO journal.

[36]  D. Beach,et al.  The fission yeast cdc2/cdc13/suc1 protein kinase: Regulation of catalytic activity and nuclear localization , 1989, Cell.

[37]  S. Reed,et al.  The Saccharomyces cerevisiae CKS1 gene, a homolog of the Schizosaccharomyces pombe suc1+ gene, encodes a subunit of the Cdc28 protein kinase complex , 1989, Molecular and cellular biology.

[38]  P. Russell,et al.  The mitotic inducer nim1 + functions in a regulatory network of protein kinase homologs controlling the initiation of mitosis , 1987, Cell.

[39]  K. Gould,et al.  Complementation of the mitotic activator, p80cdc25, by a human protein-tyrosine phosphatase , 1990, Science.

[40]  P. Nurse,et al.  A cdc2-like protein is involved in the initiation of DNA replication in Xenopus egg extracts , 1990, Cell.

[41]  S. Reed The selection of S. cerevisiae mutants defective in the start event of cell division. , 1980, Genetics.

[42]  T. Hunter,et al.  Detection and quantification of phosphotyrosine in proteins. , 1983, Methods in enzymology.

[43]  D. Beach,et al.  Activation of M-phase-specific histone H1 kinase by modification of the phosphorylation of its p34cdc2 and cyclin components. , 1990, Genes & development.

[44]  J. Jiménez,et al.  Complementation of fission yeast cdc2ts and cdc25ts mutants identifies two cell cycle genes from Drosophila: a cdc2 homologue and string. , 1990, The EMBO journal.

[45]  J. Hayles,et al.  suc1 is an essential gene involved in both the cell cycle and growth in fission yeast , 1986, The EMBO journal.

[46]  Uttam Surana,et al.  The role of CDC28 and cyclins during mitosis in the budding yeast S. cerevisiae , 1991, Cell.

[47]  R. Rai,et al.  A bifunctional gene product involved in two phases of the yeast cell cycle , 1982, Nature.

[48]  P. Nurse,et al.  Regulatory phosphorylation of the p34cdc2 protein kinase in vertebrates. , 1991, The EMBO journal.

[49]  B. Novák,et al.  The first transition point of the mutant cdc2.33 in the fission yeast Schizosaccharomyces pombe. , 1989, Journal of cell science.

[50]  P. O’Farrell,et al.  Drosophila cdc2 homologs: a functional homolog is coexpressed with a cognate variant. , 1990, The EMBO journal.

[51]  J. Potashkin,et al.  Identification of p34 and p13, human homologs of the cell cycle regulators of fission yeast encoded by cdc2 + and suc1 + , 1987, Cell.

[52]  P. Nurse,et al.  The cell cycle control gene cdc2 + of fission yeast encodes a protein kinase potentially regulated by phosphorylation , 1986, Cell.

[53]  P. Nurse,et al.  Gene required in G1 for commitment to cell cycle and in G2 for control of mitosis in fission yeast , 1981, Nature.

[54]  J. Hayles,et al.  Cloning and sequencing of the cyclin-related cdc13+ gene and a cytological study of its role in fission yeast mitosis. , 1988, Journal of cell science.

[55]  G. Fink,et al.  KAR1, a gene required for function of both intranuclear and extranuclear microtubules in yeast , 1987, Cell.

[56]  D. Beach,et al.  Involvement of cdc13+ in mitotic control in Schizosaccharomyces pombe: possible interaction of the gene product with microtubules. , 1988, The EMBO journal.

[57]  S. Reed,et al.  Dominant negative protein kinase mutations that confer a G1 arrest phenotype. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[58]  J. Labbé,et al.  Purification of MPF from starfish: Identification as the H1 histone kinase p34cdc2 and a possible mechanism for its periodic activation , 1989, Cell.

[59]  A. Nigg Structure anddevelopmental expression ofthechicken CDC2kinase , 1989 .