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Summary Expression Phenotypes Gene Literature (148) GO Terms (16) Nucleotides (388) Proteins (54) Interactants (761) Wiki
XB--941539

Papers associated with plk1



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Plk1 regulates activation of the anaphase promoting complex by phosphorylating and triggering SCFbetaTrCP-dependent destruction of the APC Inhibitor Emi1., Hansen DV, Loktev AV, Ban KH, Jackson PK., Mol Biol Cell. December 1, 2004; 15 (12): 5623-34.

Checkpoint adaptation and recovery: back with Polo after the break., van Vugt MA, Medema RH., Cell Cycle. November 1, 2004; 3 (11): 1383-6.

Timing of Plk1 and MPF activation during porcine oocyte maturation., Anger M, Klima J, Kubelka M, Prochazka R, Motlik J, Schultz RM., Mol Reprod Dev. September 1, 2004; 69 (1): 11-6.

A feedback loop in the polo-like kinase activation pathway., Erikson E, Haystead TA, Qian YW, Maller JL., J Biol Chem. July 30, 2004; 279 (31): 32219-24.

Adaptation of a DNA replication checkpoint response depends upon inactivation of Claspin by the Polo-like kinase., Yoo HY, Kumagai A, Shevchenko A, Shevchenko A, Dunphy WG., Cell. May 28, 2004; 117 (5): 575-88.

Role of Polo-like kinase in the degradation of early mitotic inhibitor 1, a regulator of the anaphase promoting complex/cyclosome., Moshe Y, Boulaire J, Pagano M, Hershko A., Proc Natl Acad Sci U S A. May 25, 2004; 101 (21): 7937-42.

The polo box is required for multiple functions of Plx1 in mitosis., Liu J, Lewellyn AL, Chen LG, Maller JL., J Biol Chem. May 14, 2004; 279 (20): 21367-73.

Polo-like kinase confers MPF autoamplification competence to growing Xenopus oocytes., Karaiskou A, Leprêtre AC, Pahlavan G, Du Pasquier D, Ozon R, Jessus C., Development. April 1, 2004; 131 (7): 1543-52.              

A Xenopus cell-free system for analysis of the Chfr ubiquitin ligase involved in control of mitotic entry., Kang D, Wong J, Fang G., Methods Mol Biol. January 1, 2004; 280 229-43.

The molecular basis for phosphodependent substrate targeting and regulation of Plks by the Polo-box domain., Elia AE, Rellos P, Haire LF, Chao JW, Ivins FJ, Hoepker K, Mohammad D, Cantley LC, Smerdon SJ, Yaffe MB., Cell. October 3, 2003; 115 (1): 83-95.

Identification of a consensus motif for Plk (Polo-like kinase) phosphorylation reveals Myt1 as a Plk1 substrate., Nakajima H, Toyoshima-Morimoto F, Taniguchi E, Nishida E., J Biol Chem. July 11, 2003; 278 (28): 25277-80.

Polo-like kinase 1 regulates Nlp, a centrosome protein involved in microtubule nucleation., Casenghi M, Meraldi P, Weinhart U, Duncan PI, Körner R, Nigg EA., Dev Cell. July 1, 2003; 5 (1): 113-25.

Cell cycle dependent expression of Plk1 in synchronized porcine fetal fibroblasts., Anger M, Kues WA, Klima J, Mielenz M, Kubelka M, Motlik J, Esner M, Dvorak P, Carnwath JW, Niemann H., Mol Reprod Dev. July 1, 2003; 65 (3): 245-53.

Stk10, a new member of the polo-like kinase kinase family highly expressed in hematopoietic tissue., Walter SA, Cutler RE, Martinez R, Gishizky M, Hill RJ., J Biol Chem. May 16, 2003; 278 (20): 18221-8.

Polo-like kinase 1 in the life and death of cancer cells., Liu X, Erikson RL., Cell Cycle. January 1, 2003; 2 (5): 424-5.

Cohesin release is required for sister chromatid resolution, but not for condensin-mediated compaction, at the onset of mitosis., Losada A, Hirano M, Hirano T., Genes Dev. December 1, 2002; 16 (23): 3004-16.

Katanin-mediated microtubule severing can be regulated by multiple mechanisms., McNally KP, Buster D, McNally FJ., Cell Motil Cytoskeleton. December 1, 2002; 53 (4): 337-49.

Phosphorylation of threonine 210 and the role of serine 137 in the regulation of mammalian polo-like kinase., Jang YJ, Ma S, Terada Y, Erikson RL., J Biol Chem. November 15, 2002; 277 (46): 44115-20.

Identification of phosphorylation sites in the polo-like kinases Plx1 and Plk1 by a novel strategy based on element and electrospray high resolution mass spectrometry., Wind M, Kelm O, Nigg EA, Lehmann WD., Proteomics. November 1, 2002; 2 (11): 1516-23.

Cell cycle-regulated phosphorylation of the Xenopus polo-like kinase Plx1., Kelm O, Wind M, Lehmann WD, Nigg EA., J Biol Chem. July 12, 2002; 277 (28): 25247-56.

Cdc5 influences phosphorylation of Net1 and disassembly of the RENT complex., Shou W, Azzam R, Chen SL, Huddleston MJ, Baskerville C, Charbonneau H, Annan RS, Carr SA, Deshaies RJ., BMC Mol Biol. April 17, 2002; 3 3.              

The checkpoint protein Chfr is a ligase that ubiquitinates Plk1 and inhibits Cdc2 at the G2 to M transition., Kang D, Chen J, Wong J, Fang G., J Cell Biol. January 21, 2002; 156 (2): 249-59.                

Cloning and characterization of Plx2 and Plx3, two additional Polo-like kinases from Xenopus laevis., Duncan PI, Pollet N, Niehrs C, Nigg EA., Exp Cell Res. October 15, 2001; 270 (1): 78-87.

The polo-like kinase Plx1 is required for activation of the phosphatase Cdc25C and cyclin B-Cdc2 in Xenopus oocytes., Qian YW, Erikson E, Taieb FE, Maller JL., Mol Biol Cell. June 1, 2001; 12 (6): 1791-9.

Regulation of Op18 during spindle assembly in Xenopus egg extracts., Budde PP, Kumagai A, Dunphy WG, Heald R., J Cell Biol. April 2, 2001; 153 (1): 149-58.              

Cyclin E uses Cdc6 as a chromatin-associated receptor required for DNA replication., Furstenthal L, Kaiser BK, Swanson C, Jackson PK., J Cell Biol. March 19, 2001; 152 (6): 1267-78.                    

Polo-like kinase 1 phosphorylates cyclin B1 and targets it to the nucleus during prophase., Toyoshima-Morimoto F, Taniguchi E, Shinya N, Iwamatsu A, Nishida E., Nature. March 8, 2001; 410 (6825): 215-20.

Interplay between Cdc2 kinase and the c-Mos/MAPK pathway between metaphase I and metaphase II in Xenopus oocytes., Frank-Vaillant M, Haccard O, Ozon R, Jessus C., Dev Biol. March 1, 2001; 231 (1): 279-88.

Dominant-negative polo-like kinase 1 induces mitotic catastrophe independent of cdc25C function., Cogswell JP, Brown CE, Bisi JE, Neill SD., Cell Growth Differ. December 1, 2000; 11 (12): 615-23.

The polo-like kinase Plx1 prevents premature inactivation of the APC(Fizzy)-dependent pathway in the early Xenopus cell cycle., Brassac T, Castro A, Lorca T, Le Peuch C, Dorée M, Labbé JC, Galas S., Oncogene. August 3, 2000; 19 (33): 3782-90.

The human polo-like kinase, PLK, regulates cdc2/cyclin B through phosphorylation and activation of the cdc25C phosphatase., Roshak AK, Capper EA, Imburgia C, Fornwald J, Scott G, Marshall LA., Cell Signal. June 1, 2000; 12 (6): 405-11.

Ste20-like kinase (SLK), a regulatory kinase for polo-like kinase (Plk) during the G2/M transition in somatic cells., Ellinger-Ziegelbauer H, Karasuyama H, Yamada E, Tsujikawa K, Todokoro K, Nishida E., Genes Cells. June 1, 2000; 5 (6): 491-8.

The critical role of the MAP kinase pathway in meiosis II in Xenopus oocytes is mediated by p90(Rsk)., Gross SD, Schwab MS, Taieb FE, Lewellyn AL, Qian YW, Maller JL., Curr Biol. April 20, 2000; 10 (8): 430-8.

The activation of MAP kinase and p34cdc2/cyclin B during the meiotic maturation of Xenopus oocytes., Palmer A, Nebreda AR., Prog Cell Cycle Res. January 1, 2000; 4 131-43.

Mitotic effects of a constitutively active mutant of the Xenopus polo-like kinase Plx1., Qian YW, Erikson E, Maller JL., Mol Cell Biol. December 1, 1999; 19 (12): 8625-32.

Phosphatase 2A and polo kinase, two antagonistic regulators of cdc25 activation and MPF auto-amplification., Karaïskou A, Jessus C, Brassac T, Ozon R., J Cell Sci. November 1, 1999; 112 ( Pt 21) 3747-56.

A p90(rsk) mutant constitutively interacting with MAP kinase uncouples MAP kinase from p34(cdc2)/cyclin B activation in Xenopus oocytes., Gavin AC, Ni Ainle A, Chierici E, Jones M, Nebreda AR., Mol Biol Cell. September 1, 1999; 10 (9): 2971-86.

Purification and cloning of a protein kinase that phosphorylates and activates the polo-like kinase Plx1., Qian YW, Erikson E, Maller JL., Science. November 27, 1998; 282 (5394): 1701-4.

MPF amplification in Xenopus oocyte extracts depends on a two-step activation of cdc25 phosphatase., Karaïskou A, Cayla X, Haccard O, Jessus C, Ozon R., Exp Cell Res. November 1, 1998; 244 (2): 491-500.

Activated polo-like kinase Plx1 is required at multiple points during mitosis in Xenopus laevis., Qian YW, Erikson E, Li C, Maller JL., Mol Cell Biol. July 1, 1998; 18 (7): 4262-71.

The Polo-like kinase Plx1 is a component of the MPF amplification loop at the G2/M-phase transition of the cell cycle in Xenopus eggs., Abrieu A, Brassac T, Galas S, Fisher D, Labbé JC, Dorée M., J Cell Sci. June 1, 1998; 111 ( Pt 12) 1751-7.

The polo-like kinase Plx1 is required for M phase exit and destruction of mitotic regulators in Xenopus egg extracts., Descombes P, Nigg EA., EMBO J. March 2, 1998; 17 (5): 1328-35.

The mitotic peptidyl-prolyl isomerase, Pin1, interacts with Cdc25 and Plx1., Crenshaw DG, Yang J, Means AR, Kornbluth S., EMBO J. March 2, 1998; 17 (5): 1315-27.

The essential mitotic peptidyl-prolyl isomerase Pin1 binds and regulates mitosis-specific phosphoproteins., Shen M, Stukenberg PT, Kirschner MW, Lu KP., Genes Dev. March 1, 1998; 12 (5): 706-20.

Plk is a functional homolog of Saccharomyces cerevisiae Cdc5, and elevated Plk activity induces multiple septation structures., Lee KS, Erikson RL., Mol Cell Biol. June 1, 1997; 17 (6): 3408-17.

Cell-cycle control: POLO-like kinases join the outer circle., Lane HA, Nigg EA., Trends Cell Biol. February 1, 1997; 7 (2): 63-8.

Dynamic changes in nuclear architecture during mitosis: on the role of protein phosphorylation in spindle assembly and chromosome segregation., Nigg EA, Blangy A, Lane HA., Exp Cell Res. December 15, 1996; 229 (2): 174-80.

Purification and molecular cloning of Plx1, a Cdc25-regulatory kinase from Xenopus egg extracts., Kumagai A, Dunphy WG., Science. September 6, 1996; 273 (5280): 1377-80.

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