In vivo regulation of cytostatic activity in Xenopus metaphase II- arrested oocytes

Developmental Biology

Volumn 185, Issue 1, 1997, Pages 55-66

  Thibier, Catherine ^a   De Smedt, Véronique ^a   Poulhe, Robert ^a   Huchon, Denise ^a   Jessus, Catherine ^a   Ozon, René ^a  

^a CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIN B; CYCLINE; MATURATION PROMOTING FACTOR; MITOGEN ACTIVATED PROTEIN KINASE; PROTEIN KINASE; UBIQUITIN PROTEIN LIGASE;

ANIMAL CELL; ARTICLE; CONTROLLED STUDY; ENZYME ACTIVITY; FEMALE; FERTILIZATION; GERMINAL VESICLE; METAPHASE; MITOSIS SPINDLE; NONHUMAN; OOCYTE DEVELOPMENT; PRIORITY JOURNAL; PROTEIN METABOLISM; PROTEIN PHOSPHORYLATION; PROTEIN SYNTHESIS; XENOPUS LAEVIS;

EID: 0031149421     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1006/dbio.1997.8543     Document Type: Article

References (51)

1. Abrieu A., Lorca T., Labbé J-C., Morin N., Keyse S., Dorée M. MAP kinase does not inactivate, but rather prevents the cyclin degradation pathway from being turned on inXenopus. J. Cell Sci. 109:1996;239-246.
2. Anderson C. W., Baum P. R., Gesteland R. F. Processing of adenovirus 2-induced proteins. J. Virol. 12:1973;241-252.
3. Charbonneau M., Grey R. D. The onset of activation responsiveness during maturation coincides with the formation of the cortical endoplasmic reticulum in oocytes ofXenopus laevis. Dev. Biol. 102:1984;90-97.
4. Choi T., Fukasawa K., Zhou R., Tessarollo L., Borror K., Reseau J., Vande Woude G. F. The mos/mitogen-activated protein kinase (MAPK) pathway regulates the size and degradation of the first polar body in maturing mouse oocytes. Proc. Natl. Acad. Sci. USA. 93:1996;7032-7035.
5. Colledge W. H., Carlton M. B. L., Udy G. B., Evans M. J. Disruption of c-mos causes parthenogenetic development of unfertilized mouse eggs. Nature. 370:1994;65-68.
6. Daar I., Nebreda A. R., Yew N., Sass P., Paules R., Santos E., Wigler M., Vande Woude G. F. The ras oncoprotein and M-phase activity. Science. 253:1991;74-76.
7. cdc2Xenopus. Int. J. Dev. Biol. 38:1994;651-659.
8. Furuno J. H., Nishizawa M., Okazaki K., Tanaka H., Iwashita J., Nakajo H., Ogawa Y., Sagata N. Suppression of DNA replication via mos function during meiotic division inXenopus. EMBO J. 13:1994;2399-2410.
9. Gabrielli B. G., Roy L. M., Maller J. L. Requirement for cdk2 in cytostatic factor-mediated metaphase II arrest. Science. 259:1993;1766-1769.
10. Gard D. L. Microtubule organization during maturation ofXenopus. Dev. Biol. 151:1992;516-530.
11. Gard D. L., Jik Cha B., Schroeder M. M. Confocal immunofluorescence microscopy of microtubules, microtubule-associated proteins, and microtubule-organizing centers during amphibian oogenesis and early development. Curr. Top. Dev. Biol. 31:1995a;383-431.
12. Gard D. L., Cha B. J., Roeder A. D. F-actin is required for spindle anchoring and rotation inXenopus. Zygote. 3:1995b;17-26.
13. Gautier J., Minshull J., Lohka M., Glotzer M., Hunt T., Maller J. L. Cyclin is a component of maturation-promoting factor fromXenopus. Cell. 60:1990;487-494.
14. Gerhart J., Wu M., Kirschner M. Cell cycle dynamics of an M-phase-specific cytoplasmic factor inXenopus laevis. J. Cell Biol. 98:1984;1247-1255.
15. Haccard O., Sarcevic B., Lewellyn A., Hartley R., Roy L., Izumi T., Erikson E., Maller J. L. Induction of metaphase arrest in cleavingXenopus. Science. 262:1993;1262-1265.
16. Hashimoto N., Watanabe N., Furuta Y., Tamamoto H., Sagata N., Yokoyama M., Okazaki K., Nagayoshi M., Takeda N., Ikawa Y., Aizawa S. Parthenogenetic activation of oocytes in c-mos-deficient mice. Nature. 370:1994;68-71.
17. Huchon D., Crozet N., Cantenot N., Ozon R. Germinal vesicle breakdown in theXenopus laevis. Reprod. Nutr. Dev. 21:1981;135-148.
18. Huchon D., Jessus C., Thibier C., Ozon R. Presence of microtubules in isolated cortices of prophase I and metaphase II oocytes inXenopus laevis. Cell Tissue Res. 254:1988;415-420.
19. Huchon D., Rime H., Jessus C., Ozon R. Control of metaphase I formation inXenopus. Biol. Cell. 77:1993;133-141.
20. Hunt T., Luca F. C., Ruderman J. V. The requirements for protein synthesis and degradation, and the control of destruction of cyclins A and B in the meiotic and mitotic cell cycles of the clam embryo. J. Cell Biol. 116:1992;707-724.
21. Jessus C., Huchon D., Ozon R. Distribution of microtubules during the breakdown of the nuclear envelope of theXenopus. Biol. Cell. 56:1986;113-120.
22. Jessus C., Ozon R. Regulation of cell divisions during oogenesis of vertebrates: TheXenopus. Comp. Biochem. Physiol. A. 106:1993;431-448.
23. cdc2Xenopus. Development. 111:1991;813-820.
24. Jessus C., Thibier C., Ozon R. Levels of microtubules during the meiotic maturation of theXenopus. J. Cell Sci. 87:1987;705-712.
25. King R. W., Peters J-M., Tugendreich S., Rolfe M., Hieter P., Kirschner M. W. A 20S complex containing CDC27 and CDC16 catalyzes the mitosis-specific conjugation of ubiquitin to cyclin B. Cell. 81:1995;279-288.
26. Kobayashi H., Minshull J., Ford C., Golsteyn R., Poon R., Hunt T. On the synthesis and destruction of A- and B-type cyclins during oogenesis and meiotic maturation inXenopus laevis. J. Cell Biol. 114:1991;755-765.
27. Kubiak J. Z., Weber M., de Pennart H., Winston N. J., Maro B. The metaphase II arrest in mouse oocytes is controlled through microtubule-dependent destruction of cyclin B in the presence of CSF. EMBO J. 12:1993;3773-3778.
28. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 227:1970;680-685.
29. MacNicol A. M., Muslin A. J., Howards E. L., Kikuchi A., MacNicol M. C., Williams L. T. Regulation of raf-1-dependent signaling during earlyXenopus. Mol. Cell. Biol. 15:1995;6686-6693.
30. Maller J. L. Maturation-promoting factor in the early days. Trends Biochem. Sci. 20:1995;524-528.
31. Masui Y. Distribution of the cytoplasmic activity inducing germinal vesicle breakdown in frog oocytes. J. Exp. Zool. 179:1972;365-378.
32. Masui Y., Markert C. L. Cytoplasmic control of nuclear behavior during meiotic maturation of frog oocytes. J. Exp. Zool. 177:1971;129-146.
33. Minshull J., Blow J. J., Hunt T. Translation of cyclin mRNA is necessary for extracts of activatedXenopus. Cell. 56:1989;947-956.
34. Minshull J., Sun H., Tonks N. K., Murray A. W. A MAP kinase-dependent spindle assembly checkpoint inXenopus. Cell. 79:1994;475-486.
35. Murray A. Cyclin ubiquitination: The destructive end of mitosis. Cell. 81:1995;149-152.
36. Murray A. W. Creative blocks: Cell cycle checkpoints and feed-back controls. Nature. 359:1992;599-604.
37. Nebreda A. R., Hunt T. The c-mos proto-oncogene protein kinase turns on and maintains the activity of MAP kinase, but not of MPF, in cell-free extracts ofXenopus. EMBO J. 12:1993;1979-1986.
38. Posada J., Yew N., Ahn N. G., Vande Woude G. F., Cooper J. A. Mos stimulates MAP kinase inXenopusin vitro. Mol. Cell. Biol. 13:1993;2546-2553.
39. Richter H-P., Hoock C., Neumcke B. Morphological and electrophysiological properties of centrifuged stratifiedXenopus. Biol. Cell. 84:1995;129-138.
40. Rime H., Huchon D., De Smedt V., Thibier C., Galaktionov K., Jessus C., Ozon R. Microinjection of cdc25 protein phosphatase intoXenopus. Biol. Cell. 82:1994;11-22.
41. Roy L. M., Haccard O., Izumi T., Lattes B. G., Lewellyn A. L., Maller J. L. Mos proto-oncogene function during oocyte maturation inXenopus. Oncogene. 12:1996;2203-2211.
42. cdc2. J. Cell Biol. 3:1991;507-514.
43. Sagata N., Watanabe N., Vande Woude W. G., Ikawa Y. The c-mos proto-oncogene product is a cytostatic factor responsible for meiotic arrest in vertebrate eggs. Nature. 342:1989;512-518.
44. Shibuya E. K., Ruderman J. V. Mos induces thein vitro. Mol. Biol. Cell. 4:1993;781-790.
45. Sudakin V., Ganoth D., Dahan A., Heller H., Hershko J., Luca F. C., Ruderman J. V., Hersko A. The cyclosome, a large complex containing cyclin-selective ubiquitin ligase activity, targets cyclins for destruction at the end of mitosis. Mol. Biol. Cell. 6:1995;185-197.
46. Taylor M. A., Smith L. D. Accumulation of free amino acids in growingXenopus laevis. Dev. Biol. 124:1987;287-290.
47. Thibier C., Denoulet P., Jessus C., Ozon R. A predominant basic α-tubulin isoform present in prophaseXenopus. Biol. Cell. 75:1992;173-180.
48. Tugendreich S., Tomkiel J., Earnshaw W., Hieter P. CDC27Hs colocalizes with CDC16Hs to the centrosome and mitotic spindle and is essential for the metaphase to anaphase transition. Cell. 81:1995;261-268.
49. Verlhac M-H., Kubiak J. Z., Weber M., Géraud G., Colledge W. H., Evans M. J., Maro B. Mos is required for MAP kinase activation and is involved in microtubule organization during meiotic maturation in the mouse. Development. 122:1996;815-822.
50. Wasserman W. J., Masui Y. Effects of cycloheximide on a cytoplasmic factor initiating meiotic maturation inXenopus. Exp. Cell Res. 91:1975;381-388.
51. Watanabe N., Vande Woude G. F., Ikawa Y., Sagata N. Specific proteolysis of the c-mos proto-oncogene product by calpain on fertilization ofXenopus. Nature. 342:1989;505-511.