Biphasic activation of Aurora-A kinase during the meiosis I-meiosis II transition in Xenopus oocytes

Molecular and Cellular Biology

Volumn 23, Issue 5, 2003, Pages 1703-1716

  Ma, Chunqi ^a   Cummings, Cathy ^a   Liu, X Johné ^a,b  

^a OTTAWA HOSPITAL RESEARCH INSTITUTE   (Canada)

^b UNIVERSITY OF OTTAWA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AURORA A KINASE; CYCLIN B; MITOGEN ACTIVATED PROTEIN KINASE; PHOSPHOTRANSFERASE; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; CELL CYCLE; CELL FUNCTION; CONFOCAL MICROSCOPY; CONTROLLED STUDY; CYTOPLASM; ENZYME ACTIVATION; ENZYME ACTIVITY; GERMINAL VESICLE; IMMUNOBLOTTING; MEIOSIS; MOLECULAR CLONING; MYRISTYLATION; NONHUMAN; OOCYTE; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; SIGNAL TRANSDUCTION; XENOPUS;

ANIMALS; CELL CYCLE PROTEINS; CYCLIN B; DNA, COMPLEMENTARY; ENZYME ACTIVATION; ENZYME INHIBITORS; FLUORESCENCE RESONANCE ENERGY TRANSFER; IMMUNOBLOTTING; MAP KINASE SIGNALING SYSTEM; MEIOSIS; MICROSCOPY, CONFOCAL; MITOSIS; MYRISTIC ACID; OOCYTES; PHOSPHORYLATION; PROTEIN BIOSYNTHESIS; PROTEIN KINASES; PROTEIN STRUCTURE, TERTIARY; PROTEIN-SERINE-THREONINE KINASES; RNA, MESSENGER; SCHIZOSACCHAROMYCES POMBE PROTEINS; SIGNAL TRANSDUCTION; TIME FACTORS; XENOPUS; XENOPUS PROTEINS;

ANIMALIA;

EID: 0037373247     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.23.5.1703-1716.2003     Document Type: Article

References (53)

1. Andresson, T., and J. V. Ruderman. 1998. The kinase Eg2 is a component of the Xenopus oocyte progesterone-activated signalling pathway. EMBO J. 17:5627-5637.
2. Aronheim, A., D. Engelberg, N. Li, N. Al-Alawi, J. Schlessinger, and M. Karin. 1994. Membrane targeting of the nucleotide exchange factor Sos is sufficient for activating the Ras signaling pathway. Cell 78:949-961.
3. Aronheim, A., E. Zandi, H. Hennemann, S. J. Elledge, and M. Karin. 1997. Isolation of an AP-1 repressor by a novel method for detecting protein-protein interactions. Mol. Cell. Biol. 17:3092-3102.
4. Bayaa, M., R. A. Booth, Y. Sheng, and X. J. Liu. 2000. The classical progesterone receptor mediates Xenopus oocyte maturation through a nongenomic mechanism. Proc. Natl. Acad. Sci. USA 97:12607-12612.
5. Birchmeier, C., D. Broek, and M. Wigler. 1985. Ras proteins can induce meiosis in Xenopus oocytes. Cell 43:615-621.
6. Bischoff, J. R., and G. D. Plowman. 1999. The aurora/Ipl1p kinase family: regulators of chromosome segregation and cytokinesis. Trends Cell Biol. 9:454-459.
7. Davis, D., and S. E. Sadler. 1992. Analysis of the p21 ras system during the development of meiotic competence in Xenopus laevis oocytes. Dev. Biol. 149:1-7.
8. Elinson, R. P. 1985. Changes in levels of polymeric tubulin associated with activation and dorsoventral polarization of the frog egg. Dev. Biol. 109:224-233.
9. Farruggio, D. C., F. M. Townsley, and J. V. Ruderman. 1999. Cdc20 associates with the kinase aurora2/Aik. Proc. Natl. Acad. Sci. USA 96:7306-7311.
10. Ferrell, J. E. 2002. Self-perpetuating states in signal transduction: positive feedback, double-negative feedback and bistability. Curr. Opin. Cell Biol. 14:140-148.
11. Ferrell, J. E. Jr., and E. M. Machleder. 1998. The biochemical basis of an all-or-none cell fate switch in Xenopus oocytes. Science 280:895-898.
12. Francisco, L., W. Wang, and C. S. M. Chan. 1994. Type 1 protein phosphatase acts in opposition to Ipl1 protein kinase in regulating yeast chromosome segregation. Mol. Cell. Biol. 14:4731-4740.
13. Frank-Vaillant, M., O. Haccard, C. Thibier, R. Ozon, Y. Arlot-Bonnemains, C. Prigent, and C. Jessus. 2000. Progesterone regulates the accumulation and the activation of Eg2 kinase in Xenopus oocytes. J. Cell Sci. 113:1127-1138.
14. Furuno, N., M. Nishizawa, K. Okazaki, H. Tanaka, J. Iwashita, N. Nakajo, Y. Ogawa, and N. Sagata. 1994. Suppression of DNA replication via Mos function during meiotic divisions in Xenopus oocytes. EMBO J. 13:2399-2410.
15. Gard, D. L. 1992. Microtubule organization during maturation of Xenopus oocytes: assembly and rotation of the meiotic spindle. Dev. Biol. 151:516-530.
16. Gawantka, V., H. Ellinger-Ziegelbauer, and P. Hausen. 1992. 1-integrin is a material that is inserted into all newly formed plasma membrane during early Xenopus embryogenesis. Development 115:595-605.
17. Gerhart, J., M. Wu, and M. Kirschner. 1984. Cell cycle dynamics of an M-phase-specific cytoplasmic factor in Xenopus laevis oocytes and eggs. J. Cell Biol. 98:1247-1255.
18. Giet, R., and C. Prigent. 1999. Aurora/Ipl1p-related kinases, a new oncogenic family of mitotic serine/threonine kinases. J. Cell Sci. 112:3591-3601.
19. Glover, D. M., M. H. Leibowitz, D. A. McLean, and H. Parry. 1995. Mutations in aurora prevent centrosome separation leading the formation of monopolar spindles. Cell 81:95-105.
20. Groisman, I., Y. S. Huang, R. Mendez, Q. Cao, W. Theurkauf, and J. D. Richter. 2000. CPEB, maskin, and cyclin B1 mRNA at the mitotic apparatus: implications for local translational control of cell division. Cell 103:435-447.
21. Rsk. Curr. Biol. 10:430-438.
22. Guan, K., and J. E. Dixon. 1991. Eukaryotic proteins expressed in Escherichia coli: an improved thrombin cleavage and purification procedure of fusion proteins with glutathione S-transferase. Anal. Biochem. 192:262-267.
23. Hannak, E., M. Kirkham, A. A. Hyman, and K. Oegema. 2001. Aurora-A kinase is required for centrosome maturation in Caenorhabditis elegans. J. Cell Biol. 155:1109-1116.
24. Harlow, E., and D. Lane. 1988. Antibodies: a laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
25. Hodgman, R., J. Tay, R. Mendez, and J. D. Richter. 2001. CPEB phosphorylation and cytoplasmic polyadenylation are catalyzed by the kinase IAK1/Eg2 in maturing mouse oocytes. Development 128:2815-2822.
26. Huang, C. Y., and J. E. Ferrell, Jr. 1996. Ultrasensitivity in the mitogen-activated protein kinase cascade. Proc. Natl. Acad. Sci. USA 93:10078-10083.
27. Mm exchange factor by muscarinic receptor and G-protein βgamma subunits. Nature 382:268-272.
28. Meijer, L., A. Borgne, O. Mulner, J. P. Chong, J. J. Blow, N. Inagaki, M. Inagaki, J. G. Delcros, and J. P. Moulinoux. 1997. Biochemical and cellular effects of roscovitine, a potent and selective inhibitor of the cyclin-dependent kinases cdc2, cdk2 and cdk5. Eur. J. Biochem. 243:527-536.
29. Mendez, R., D. Barnard, and J. D. Richter. 2002. Differential mRNA translation and meiotic progression require Cdc2-mediated CPEB destruction. EMBO J. 21:1833-1844.
30. Mendez, R., L. E. Hake, T. Andresson, L. E. Littlepage, J. V. Ruderman, and J. D. Richter. 2000. Phosphorylation of CPE binding factor by Eg2 regulates translation of c-mos mRNA. Nature 404:302-307.
31. Mendez, R., K. G. K. Murthy, K. Ryan, J. L. Manley, and J. D. Richter. 2000. Phosphorylation of CPEB by Eg2 mediates the recruitment of CPSF into an active cytoplasmic polyadenylation complex. Mol. Cell 6:1253-1259.
32. Mochizuki, N., S. Yamashita, K. Kurokawa, Y. Ohba, T. Nagai, A. Miyawaki, and M. Matsuda. 2001. Spatio-temporal images of growth-factor-induced activation of Ras and Rap1. Nature 411:1065-1068.
33. Mora, S., P. Kaliman, J. Chillaron, X. Testar, M. Palacin, and A. Zorzano. 1995. Insulin and insulin-like growth factor 1 (IGF-1) stimulate GLUT4 glucose transporter translocation in Xenopus oocytes. Biochem. J. 311:59-65.
34. Nebreda, A. R., and T. Hunt. 1993. The c-mos proto-oncogene protein kinase turns on and maintains the activity of MAP kinase, but not MPF, in cell-free extracts of Xenopus oocytes and eggs. EMBO J. 12:1979-1986.
35. Nigg, E. A. 2001. Mitotic kinases as regulators of cell division and its checkpoints. Nat. Rev. Mol. Cell. Biol. 2:21-32.
36. Ohan, N., Y. Agazie, C. Cummings, R. Booth, M. Bayaa, and X. J. Liu. 1999. Rho-associated protein kinase a potentiates insulin-induced MAP kinase activation in Xenopus oocytes. J. Cell Sci. 112:2177-2184.
37. Peter, M., A. Castro, T. Lorca, C. Le Peuch, L. Magnaghi-Jaulin, M. Doree, and J. C. Labbe. 2001. The APC is dispensable for first meiotic anaphase in Xenopus oocytes. Nat. Cell Biol. 3:83-87.
38. Peter, M., J. C. Labbe, M. Doree, and E. Mandart. 2002. A new role for Mos in Xenopus oocyte maturation: targeting Myt1 independently of MAPK. Development 129:2129-2139.
39. Posada, J., and J. A. Cooper. 1992. Requirements for phosphorylation of MAP kinase during meiosis in Xenopus oocytes. Science 255:212-215.
40. Powers, S., K. O'Neill, and M. Wigler. 1989. Dominant yeast and mammalian RAS mutations that interfere with the CDC25-dependent activation of wildtype RAS in Saccharomyces cerevisiae. Mol. Cell. Biol. 9:390-395.
41. Raff, J. W., K. Jeffers, and J. Y. Huang. 2002. The roles of Fzy/Cdc20 and Fzr/Cdh1 in regulating the destruction of cyclin B in space and time. J. Cell Biol. 157:1139-1149.
42. Reverte, C. G., M. D. Ahearn, and L. E. Hake. 2001. CPEB degradation during Xenopus oocyte maturation requires a PEST domain and the 26S proteasome. Dev. Biol. 231:447-458.
43. Roghi, C., R. Giet, R. Uzbekov, N. Morin, I. Chartrain, R. Le Guellec, A. Couturier, M. Doree, M. Philippe, and C. Prigent. 1998. The Xenopus protein kinase pEg2 associates with the centrosome in a cell cycle-dependent manner, binds to the spindle microtubules and is involved in bipolar mitotic spindle assembly. J. Cell Sci. 111:557-572.
44. Schmitt, A., and A. R. Nebreda. 2002. Signalling pathways in oocyte meiotic maturation. J. Cell Sci. 115:2457-2459.
45. Schumacher, J. M., N. Ashcroft, P. J. Donovan, and A. Golden. 1998. A highly conserved centrosomal kinase, AIR-1, is required for accurate cell cycle progression and segregation of developmental factors in Caenorhabditis elegans embryos. Development 125:4391-4402.
46. Schumacher, J. M., A. Golden, and P. J. Donovan. 1998. AIR-2: an aurora/Ipl1-related protein kinase associated with chromosomes and midbody microtubules is required for polar body extrusion and cytokinesis in Caenorhabditis elegans embryos. J. Cell Biol. 143:1635-1646.
47. Rsk during Xenopus oocyte maturation. Curr. Biol. 11:141-150.
48. Shou, C., C. L. Farnsworth, B. G. Neel, and L. A. Feig. 1992. Molecular cloning of cDNAs encoding a guanine-nucleotide-releasing factor for Ras p21. Nature 358:351-354.
49. Songyang, Z., K. P. Lu, Y. T. Kwon, L.-H. Tsai, O. Filhol, C. Cochet, D. A. Brickey, T. R. Soderling, C. Bartleson, D. J. Graves, A. J. DeMaggio, M. F. Hoekstra, J. Blenis, T. Hunter, and L. C. Cantley. 1996. A structural basis for substrate specificities of protein Ser/Thr kinases: primary sequence preference of casein kinase I and II, NIMA, phosphorylase kinase, calmodulin-dependent kinase II, CDK5, and Erk1. Mol. Cell. Biol. 16:6486-6493.
50. Taieb, F. E., S. D. Gross, A. L. Lewellyn, and J. L. Maller. 2001. Activation of the anaphase-promoting complex and degradation of cyclin B is not required for progression from Meiosis I to II in Xenopus oocytes. Curr. Biol. 11:508-513.
51. Turner, D. L., and H. Weintraub. 1994. Expression of achaete-scute homology 3 in Xenopus embryos converts ectodermal cells to a neural fate. Genes Dev. 8:1434-1447.
52. Vallette, F., E. Mege, A. Reiss, and M. Adesnik. 1989. Construction of mutant and chimeric genes using the polymerase chain reaction. Nucleic Acids Res. 17:723-733.
53. Vojtek, A. B., S. M. Hollenberg, and J. A. Cooper. 1993. Mammalian Ras interacts directly with serine/threonine kinase Raf. Cell 74:205-214.