Development of pig oocytes activated by stimulation of an exogenous G protein-coupled receptor

Biology of Reproduction

Volumn 59, Issue 3, 1998, Pages 655-660

  Kim, Jae Hwan ^a   Macháty, Zoltán ^a   Cabot, Ryan A ^a   Han, Yong Mahn ^a   Do, Hyun Jin ^a   Prather, Randall S ^a  

^a UNIVERSITY OF MISSOURI   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLCHOLINE; CHOLINERGIC RECEPTOR; GUANINE NUCLEOTIDE BINDING PROTEIN; MESSENGER RNA; MUSCARINIC RECEPTOR; PROTEIN;

ANIMAL CELL; ARTICLE; BLASTOCYST; EXOCYTOSIS; FEMALE; FERTILIZATION; MITOCHONDRION; NONHUMAN; NUCLEOLUS; OOCYTE; OOCYTE DEVELOPMENT; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PRONUCLEUS; SIGNAL TRANSDUCTION; SWINE; TRANSMISSION ELECTRON MICROSCOPY;

ANIMALIA; SUS SCROFA;

EID: 0031853255     PISSN: 00063363     EISSN: None     Source Type: Journal    
DOI: 10.1095/biolreprod59.3.655     Document Type: Article

References (33)

1. Schultz RM, Kopf GS. Molecular basis of mammalian egg activation. Curr Top Dev Biol 1995; 30:21-62.
2. Stice SL, Robl JM. Activation of mammalian oocytes by a factor obtained from rabbit sperm. Mol Reprod Dev 1990; 25:272-280.
3. Swann K. Calcium oscillations and sensitization of calcium release in unfertilized mouse eggs injected with a sperm factor. Cell Calcium 1994; 15:331-339.
4. Parrington J, Swann K, Shevchenko VI, Sesay AK, Lai FA. Calcium oscillations in mammalian eggs triggered by soluble sperm protein. Nature 1996; 379:364-368.
5. Turner PR, Jaffe LA, Fein A. Regulation of cortical vesicle exocytosis in sea urchin eggs by inositol 1,4,5-trisphosphate and GTP-binding protein. J Cell Biol 1986; 102:70-76.
6. Miyazaki S. Inositol 1,4,5-trisphosphate-induced calcium release and guanine nucleotide-binding protein-mediated periodic calcium rises in golden hamster eggs. J Cell Biol 1988; 106:345-353.
7. Kline D, Kopf GS, Muncy LF, Jaffe LA. Evidence for the involvement of a pertussis toxin-insensitive G-protein in egg activation of the frog, Xenopus laevis. Dev Biol 1991; 143:218-229.
8. Macháty Z, Mayes MA, Prather RS. Parthenogenetic activation of porcine oocytes with guanosine-5′-O-(3′-thiotriphosphate). Biol Reprod 1995; 52:753-758.
9. Kline D, Simoncini L, Mandel G, Maue RA, Kado RT, Jaffe LA. Fertilization events induced by neurotransmitters after injection of mRNA in Xenopus eggs. Science 1988; 241:464-467.
10. f conversion and pronuclear formation in eggs expressing a functional m1 muscarinic receptor. Dev Biol 1992; 151:288-296.
11. Moore GD, Kopf GS, Schultz RM. Complete mouse egg activation in the absence of sperm by stimulation of an exogenous G protein-coupled receptor. Dev Biol 1993; 159:669-678.
12. Machaty Z, Mayes MA, Kovács LG, Balatti PA, Kim J-H, Prather RS. Activation of porcine oocytes via an exogenously introduced rat muscarinic M1 receptor. Biol Reprod 1997; 57:85-91.
13. Bonner TI, Buckley NJ, Young AC, Brann MR. Identification of a family of muscarinic acetylcholine receptor genes. Science 1987; 237: 527-532.
14. Bavister BD, Leibfried ML, Liebermann G. Development of preimplantation embryos of the golden hamster in a defined culture medium. Biol Reprod 1983; 28:235-247.
15. Hafez ESE. Transport and survival of gametes. In: Hafez ESE (ed.), Reproduction in Farm Animals, 5th ed. Philadelphia: Lea & Febiger; 1987: 168-188.
16. Ott RL. An introduction to statistical methods and data analysis. Fourth edition. Belmont, CA: Wadsworth, Inc.; 1993.
17. Hepler JR, Gilman AG. G proteins. TIBS 1992; 17:383-387.
18. Wess J. Molecular basis of muscarinic acetylcholine receptor function. TIPS 1993; 14:308-313.
19. Berridge MJ. Inositol trisphosphate and calcium signalling. Nature 1993; 361:315-325.
20. Felder CC. Muscarinic acetylcholine receptors: signal transduction through multiple effectors. FASEB J 1995; 9:619-625.
21. Kline D, Kline J. Repetitive calcium transients and the role of calcium in exocytosis and cell cycle activation in the mouse egg. Dev Biol 1992; 149:80-89.
22. Uehara T, Yanagimachi R. Activation of hamster eggs by pricking. J Exp Zool 1977; 199:269-274.
23. Cascio SM, Wassarman PM. Program of early development in the mammalian: post-transcriptional control of a class of proteins synthesized by mouse oocytes and early embryos. Dev Biol 1982; 89:397-408.
24. Ding J, Clarke N, Nagai T, Moor RM. Protein and nuclear changes in pig eggs at fertilization. Mol Reprod Dev 1992; 31:287-296.
25. Sun FZ, Hoyland J, Huang X, Mason W, Moor RM. A comparison of intracellular changes in porcine eggs after fertilization and electroactivation. Development 1992; 115:947-956.
26. Macháty Z, Funahashi H, Mayes MA, Day BN, Prather RS. Effects of injecting calcium chloride into in vitro-matured porcine oocytes. Biol Reprod 1996; 54:316-322.
27. Mayes MA, Stogsdill PL, Prather RS. Parthenogenic activation of pig oocytes by protein kinase inhibition. Biol Reprod 1995; 53:270-275.
28. Schoenbeck RA, Peters MS, Rickords LF, Stumpf TT, Prather RS. Characterization of deoxyribonucleic acid synthesis and the transition from maternal to embryonic control in the 4-cell porcine embryo. Biol Reprod 1992; 47:1118-1125.
29. Norberg HS. Ultrastructural aspects of the preattached pig embryo: cleavage and early blastocyst stages. Z Anat Entwicklungsgesch 1973; 143:95-114.
30. Stern S, Biggers JD, Anderson E. Mitochondria and early development of the mouse. J Exp Zool 1971; 176:179-192.
31. Mills RM, Brinster RL. Oxygen consumption of preimplantation mouse embryos. Exp Cell Res 1967; 47:337-344.
32. Wales RG, Biggers JD. The permeability of two- and eight-cell mouse embryos to L-malic acid. J Reprod Fertil 1968; 15:103-111.
33. Krause WJ, Charlson EJ, Sherman DM, Day BN. Three-dimensional reconstruction using a computer graphics system: application to mitochondrial aggregates in porcine oocytes, zygotes, and early embryos using a personal computer. Zool Anz 1992; 229:21-36.