Dynamics of maturation-promoting factor and its constituent proteins during in vitro maturation of bovine oocytes

Biology of Reproduction

Volumn 56, Issue 1, 1997, Pages 253-259

  Wu, Bin ^a,c   Ignotz, George ^a   Currie, W Bruce ^a   Yang, Xiangzhong ^a,b  

^a Department of Obstetrics Gynecology   (United States)

^b UNIVERSITY OF CONNECTICUT   (United States)

^c UNIVERSITY OF GUELPH   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CYCLIN DEPENDENT KINASE; MATURATION PROMOTING FACTOR;

ANAPHASE; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CELL MATURATION; ENZYME ACTIVITY; GERMINAL VESICLE; IMMUNOBLOTTING; IMMUNOPRECIPITATION; MEIOSIS; MITOSIS; NONHUMAN; OOCYTE MATURATION; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN SYNTHESIS; TELOPHASE;

ANIMALS; CATTLE; CYCLIN-DEPENDENT KINASES; CYCLINS; FEMALE; MATURATION-PROMOTING FACTOR; MEIOSIS; OOCYTES; PROTEIN KINASES;

EID: 0031012063     PISSN: 00063363     EISSN: None     Source Type: Journal    
DOI: 10.1095/biolreprod56.1.253     Document Type: Article

References (65)

1. Smith LD. The induction of oocyte maturation: transmembrane signaling events and regulation of the cell cycle. Development 1989; 107: 685-699.
2. Masui Y, Marken CL. Cytoplasmic control of nuclear behavior during meiotic maturation of frog oocytes. J Exp Zool 1971; 177:129-146.
3. Smith LD, Ecker RE. Regulatory processes in the maturation and early cleavage of amphibian eggs. Curr Top Dev Biol 1971; 5:1-38.
4. Lohka MJ, Hayes MK, Maller JL. Purification of maturation-promoting factor, an intracellular regulator of early mitotic events. Proc Natl Acad Sci USA 1988; 85:3009-3013.
5. Gautier J, Minshull J, Lohka M, Giotzer M, Hunt T, Maller JL. Cyclin is a component of maturation-promoting factor from Xenopus. Cell 1990; 60:487-494.
6. Murray AW. Creative blocks: cell-cycle checkpoints and feedback controls. Nature 1992; 359:599-604.
7. Kishimoto T, Kanatani H. Cytoplasmic factor responsible for germinal vesicle breakdown and meiotic maturation in starfish oocytes. Nature 1976; 221:273-274.
8. Murray AW, Kirschner MW. Domineos and clocks: the union of two views of the cell cycle. Science 1989; 246:614-621.
9. Murray AW, Solomon MJ, Kirschner MW. The role of cyclin synthesis and degradation in the control of maturation promoting factor activity. Nature 1989; 339:280-286.
10. Nurse P. Universal control mechanism regulating onset of M-phase. Nature 1990; 344:503-507.
11. Motlik J, Kubelka M. Cell-cycle aspects of growth and maturation of mammalian oocytes. Mol Reprod Dev 1990; 27:366-375.
12. Parrish JJ, Kim CI, Bae IH. Current concepts of cell-cycle regulation and its relationship to oocyte maturation, fertilization and embryo development. Theriogenology 1992; 38:277-296.
13. Lewin B. Driving the cell cycle: M phase kinase, its partners and substrates. Cell 1990; 61:743-752.
14. Norbury C, Nurse P. Animal cell cycle and their control. Annu Rev Biochem 1992; 61:441-470.
15. Yew N, Strobel M, Vande Woude GF. Mos and cell cycle: the molecular basis of the transformed phenotype. Curr Opin Genet Dev 1993; 3:19-25.
16. Homa ST. Calcium and meiotic maturation of the mammalian oocyte. Mol Reprod Dev 1995; 40:122-134.
17. Arion D, Meijer L, Brizuela L, Beach D. cdc2 is a component of the M phase-specific histone H1 kinase: evidence for identity with MPF. Cell 1988; 55:371-378.
18. Draetta G, Luca F, Westendorf J, Brizuela L, Ruderman J, Beach D. cdc2 protein kinase is complexed with both cyclin A and B: evidence for proteolytic inactivation of MPF. Cell 1989; 56:829-838.
19. Moor R, Hutchings A, Hawkins C, Jung T. Towards a molecular understanding of meiosis in domestic animals. In: Lauria A, Gandolfi F (eds.), Embryonic Development and Manipulation in Animal Production Trends in Research and Applications. London: Portland Press; 1992: 1-15.
20. Hashimoto N, Kishimoto T. Regulation of meiotic metaphase by a cytoplasmic maturation-promoting factor during mouse oocyte maturation. Dev Biol 1988; 126:242-252.
21. Fulka J Jr, Flechon JE, Motlik J, Fulka J. Does autocatalytic amplification of maturating-promoting factor (MPF) exist in mammalian oocytes? Gamete Res 1988; 21:185-192.
22. Fulka J Jr, Jung T, Moor RM. The fall of biological maturation promoting factor (MPF) and histone H1 kinase activity during anaphase and telophase in mouse oocytes. Mol Reprod Dev 1992; 32:378-382.
23. Mattioli M, Galeati G, Bacci ML, Barboni B. Change in maturation-promoting activity in the cytoplasm of pig oocytes throughout maturation. Mol Reprod Dev 1991; 30:119-125.
24. Naito K, Toyoda Y. Fluctuation of histone H1 kinase activity during meiotic maturation in porcine oocytes. J Reprod Fertil 1991; 93:467-473.
25. Christmann L, Jung T, Moor RM. MPF components and meiotic competence in growing pig oocytes. Mol Reprod Dev 1994; 38:85-90.
26. Kikuchi K, Naito K, Daen FP, Izaike Y, Toyoda Y. Histone H1 kinase activity during in vitro fertilization of pig follicular oocytes matured in vitro. Theriogenology 1995; 43:523-532.
27. Jelinkova L, Kubelka M, Motlik J, Guerrier P. Chromatin condensation and histone H1 kinase activity during growth and maturation of rabbit oocytes. Mol Reprod Dev 1994; 37:210-215.
28. Campbell KHS, Ritchie WA, Wilmut I. Nuclear-cytoplasmic interactions during the first cell cycle of nuclear transfer reconstructed bovine embryos: implications for deoxyribonucleic acid replication and development. Biol Reprod 1993; 49:933-942.
29. Collas P, Sullivan EJ, Barnes FL. Histone H1 activity in bovine oocytes following calcium stimulation. Mol Reprod Dev 1993; 34:224-231.
30. Evans T, Rosenthal ET, Youngblom J, Distel D, Hunt T. Cyclin: a protein specified by maternal mRNA in sea urchin eggs that is destroyed at each cleavage division. Cell 1983; 33:389-396.
31. Hunter T. Oncogenes and cell proliferation. Curr Opin Genet Dev 1993; 3:1-4.
32. 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 in Xenopus laevis. J Cell Biol 1991; 114: 755-765.
33. Chapman DL, Wolgemuth DJ. Isolation of the murine cyclin B2 cDNA and characterization of the lineage and temporal specificity of expression of the B1 and B2 cyclins during oogenesis, spermatogenesis and early embryogenesis. Development 1993; 118:229-240.
34. Westendorf JM, Swenson KI, Ruderman JV. The role of cyclin B in meiosis I. J Cell Biol 1989; 108:1431-1444.
35. Minshull J. Cyclin synthesis: who needs it? Bioessays 1993; 15:149-155.
36. Yang X, Jiang S, Foote RH. Bovine oocyte development following different oocyte maturation and sperm capacitation procedures. Mol Reprod Dev 1993; 34:94-100.
37. Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 1970; 277:680-685.
38. Towbin H, Staehelin T, Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci USA 1979; 76:4350-4354.
39. Harlow E, Lane D. Immunoprecipitation. In: Antibody, A Laboratory Manual. New York: Cold Spring Harbor Laboratory; 1988: 421-469.
40. Bonner WM, Laskey RA. A film detection method for tritium labelled proteins and nucleic acids in polyacrylamide gels. Eur J Biochem 1974; 46:83-88.
41. 14C in polyacrylamide gels by fluorography. Eur J Biochem 1975; 56:335-341.
42. Sirard MA, Florman HM, Leibfried-Rutledge ML, Barnes FL, Sims ML, First NL. Timing of nuclear progression and protein synthesis necessary for meiotic maturation of bovine oocytes. Biol Reprod 1989; 40:1257-1263.
43. Shamsuddin M, Larsson B, Rodriguez-Martinez H. Maturation-related changes in bovine oocytes under different culture conditions. Anim Reprod Sci 1993; 31:49-60.
44. Nagai T. Parthenogenetic activation of cattle follicular oocytes in vitro with ethanol. Gamete Res 1987; 16:243-249.
45. Ware CB, Barnes FL, Maiki-Laurila M, First NL. Age dependence of bovine oocyte activation. Gamete Res 1989; 22:265-275.
46. Yang X, Jiang S, Kovacs A, Foote RH. Age dependent activation, enucleation and nuclear transfer of bovine oocytes matured in vitro and in vivo. Biol Reprod 1991; 44(suppl 1):141.
47. Hampl A, Eppig JJ. Translation regulation of the gradual increase in histone H1 kinase activity in maturating mouse oocytes. Mol Reprod Dev 1995; 40:9-15.
48. Kubelka M, Rimkevicava Z, Guerrier P, Motlik J. Inhibition of protein synthesis affects histone H1 kinase, but not chromosome condensation activity, during the first meiotic division of pig oocytes. Mol Reprod Dev 1995; 41:63-69.
49. Levesque JT, Sirard MA. Effects of different kinases and phosphatases on nuclear and cytoplasmic maturation of bovine oocytes. Mol Reprod Dev 1995; 42:114-121.
50. Talemoto H, Terada T. Activation of p34cdc2 kinase around the meiotic resumption in bovine oocytes cultured in vitro. Theriogenology 1996; 45:427-437.
51. Levesque JT, Sirard MA. Meiotic resumption is mediated by the accumulation of cyclin B in bovine immature oocytes. Theriogenology 1996; 45:188.
52. cdc2 protein kinase activity in meiotic and mitotic cell cycle in mouse oocytes and embryos. Development 1991; 113: 789-795.
53. Minshull J, Blow JJ, Hunt T. Translation of cyclin mRNA is necessary for extracts of activated Xenopus eggs to enter mitosis. Cell 1989; 56: 947-956.
54. Murray AW. The cell cycle as a cdc2 cycle. Nature 1989; 342:14-15.
55. Hampl A, Eppig JJ. Analysis of the mechanism(s) of metaphase I arrest in maturing mouse oocytes. Development 1995; 121:925-933.
56. Tatemoto H, Horiuchi T. Requirement for protein synthesis during the onset of meiosis in bovine oocytes and its involvement in the autocatalytic amplification of maturation-promoting factor. Mol Reprod Dev 1995; 41:47-53.
57. Gould KL, Nurse P. Tyrosine phosphorylation of the fission yeast cdc2 protein kinase regulates entry into mitosis. Nature 1988; 342:39-45.
58. cdc2. Cell 1990; 63:1013-1024.
59. Sagata N, Watanabe N, Vande Woude GF, Ikawa Y. The products of the mos proto-oncogene product is a cytostatic factor responsible for meiosis arrest in vertebrate eggs. Nature 1989; 342:512-518.
60. Sagata N. Meiotic metaphase arrest in animal oocytes: its mechanisms and biological significance. Trends Cell Biol 1996; 6:22-28.
61. cdc2 and P33CDK2 in regulation of metaphase II arrest in bovine oocytes. Theriogenology 1996; 45:157.
62. Wu B, Ignotz GG, Currie BW, Yang X. Identification of c-mos protooncoprotein and its association with β-tubulin in mature bovine oocytes. Theriogenology 1995; 43:356.
63. Tatemoto H, Terada T. On the c-mos proto-oncogene product during meiotic maturation in bovine oocytes culture in vitro. J Exp Zool 1995; 272:159-162.
64. Watanabe N, Vande Woude GF, Ikawa Y, Sagata N. Specific proteolysis of the c-mos proto-oncogene product by calpain on fertilization of Xenopus eggs. Nature 1989; 342:505-511.
65. Wu B, Ignotz G, Currie WB, Yang X. Expression of Mos proto-oncoprotein in bovine oocytes during maturation in vitro. Biol Reprod 1997; 56:260-265.