Progesterone regulates the accumulation and the activation of Eg2 kinase in Xenopus oocytes

Journal of Cell Science

Volumn 113, Issue 7, 2000, Pages 1127-1138

  Frank Vaillant, Marie ^a   Haccard, Olivier ^a   Thibier, Catherine ^a   Ozon, René ^a   Arlot Bonnemains, Yannick ^b   Prigent, Claude ^b   Jessus, Catherine ^a  

^a SORBONNE UNIVERSITÉ   (France)

^b UNIVERSITÉ DE RENNES 1   (France)

Author keywords

Aurora kinase; Cdc2; Eg2; PKA; Progesterone; Xenopus oocyte

Indexed keywords

CELL CYCLE PROTEIN; CYCLIC AMP DEPENDENT PROTEIN KINASE; PROGESTERONE; PROTEIN KINASE;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; ENZYME ACTIVATION; FEMALE; HORMONAL REGULATION; METHYLATION; NONHUMAN; OOCYTE; PARTHENOGENESIS; POLYADENYLATION; PRIORITY JOURNAL; PROPHASE; XENOPUS;

ANIMALS; CDC2 PROTEIN KINASE; CELL CYCLE PROTEINS; CELL DIFFERENTIATION; CYCLIC AMP-DEPENDENT PROTEIN KINASES; ENZYME ACTIVATION; FEMALE; MEIOSIS; OOCYTES; PARTHENOGENESIS; PHOSPHORYLATION; POLY A; PROGESTERONE; PROTEIN KINASES; PROTEIN-SERINE-THREONINE KINASES; RIBOSE; RNA CAPS; RNA, MESSENGER; XENOPUS LAEVIS; XENOPUS PROTEINS;

ANIMALIA;

EID: 0034015512     PISSN: 00219533     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (14)

1. Anderson, C. W., Baum, P. R. and Gesteland, R. F. (1973). Processing of adenovirus 2-induced proteins. J. Virol. 12, 241-252.
2. Andresson, T. and Ruderman, J. V. (1998). The kinase Eg2 is a component of the Xenopus oocyte progesterone-activated signalins pathway. EMBO J. 17, 5627-5637.
3. Ballantyne, S., Daniel, D. L. and Wickens, IM. (1997). A dependent pathway of cytoplasmic polyadenylation reactions linked to cell cycle control by cmos and CDK1 activation. Mol. Biol. Cell 8, 1633-1648.
4. Barkoff, A., Ballantyne, S. and Wickens, M. (1998). Meiotic maturation in Xenopus requires polyadenylation of multiple mRNAs. EMBO J. 17, 3168-3175.
5. Barrett, A. J., Kembhavi, A. A., Brown, M. A., Kirschke, H., Knight, C. G., Tamai, M. and Hanada, K. (1982). L-trans-Epoxysuccinyl-leucylamido(4-guanidino)butane (E-64) and its analogues as inhibitors of cysteine proteinases including cathepsins B, H and L. Biochem. J. 201, 189-198.
6. Bialojan, C. and Takai, A. (1988). Inhibitory effect of a marine-sponge toxin, okadaic acid, on protein phosphatase. Biochem. J. 256, 283-290.
7. Bischoff, J. R., Anderson, L., Zhu, Y., Mossie, K., Ng, L., Souza, B., Schryver, B., Flanagan, P., Clairvoyant, F., Ginther, C. et al. (1998). A homologue of Drosophila aurora kinase is oncogenic and amplified in human colorectal cancers. EMBO J. 17, 3052-3065.
8. Bisehoff, J. R. and Plowman, G. D. (1999). The Aurora/Ipl1p kinase family: regulators of chromosome segregation and cytokinesis. Trends Cell Biol. 9, 454-459.
9. Farruggio, D. C., Townsley, F. M. and Ruderman, J. V. (1999). Cdc20 associates with the kinase aurora2/Aik. Proc. Nat. Acad. Sci. USA 96, 7306-7311.
10. Frank-Vaillant, M., Jessus, C., Ozon, R., Maller, J. L. and Haccard, O. (1999). Two distinct mechanisms control the accumulation of cyclin B1 and Mos in Xenopus oocytes in response to progesterone. Mol. Biol. Cell 10, 3279-3288.
11. Furuno, N., Nishizawa, M., Okazaki, K., Tanaka, H., Iwashita, J., Nakajo, N., Ogawa, Y. and Sagata, N. (1994). Suppression of DNA replication via Mos function during meiotic divisions in Xenopus oocytes. EMBO J. 13, 2399-2410.
12. Gard, D. L. (1992). Microtubule organization during maturation of Xenopus oocytes - assembly and rotation of the meiotic spindles. Dev. Biol. 151, 516-530.
13. Yanai, A., Arama, E., Kilfin, G. and Motro, B. (1997). Aykl, a novel mammalian gene related to Drosophila aurora centrosome separation kinase, is specifically expressed during meiosis. Oncogene 14, 2943-2950.
14. Zhou, H., Kuang, J., Zhong, L., Kuo, W. L., Gray, J. W., Sahin, A., Brinkley, B. R. and Sen, S. (1998). Tumour amplified kinase STK15/BTAK induces centrosome amplification, aneuploidy and transformation. Nature Genet. 20, 189-193.