CAPACITY OF MOUSE OOCYTES TO BECOME ACTIVATED DEPENDS ON COMPLETION OF CYTOPLASMIC BUT NOT NUCLEAR MEIOTIC MATURATION

被引:18
作者
MCCONNELL, JML
CAMPBELL, L
VINCENT, C
机构
[1] Department of Anatomy, University of Cambridge, Cambridge
关键词
ACTIVATION; CALCIUM IONOPHORE; MOUSE OOCYTE;
D O I
10.1017/S0967199400002379
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The ability of mouse oocytes to become activated after exposure to the calcium ionophore A23187 has been investigated at different stages of meiotic maturation. The potential to respond to ionophore has been studied in relation to the time since resumption of meiotic maturation, the chromosomal conformation of the DNA within each cell and the protein synthetic profile of the maturing oocyte. Our studies demonstrate that when maturing oocytes from an MF1 strain of mice were treated with A23187 activation occurred only in oocytes which had reached second meiotic metaphase (MII). However, development of the ability to respond to ionophore was not dependent on an orderly progression through normal chromosomal rearrangements such as separation at metaphase I (MI) and subsequent polar body extrusion, since these processes could be prevented and the capacity to be activated became apparent in such oocytes at a time when control cells had reached MII. These data suggest that the ability to respond to ionophore depends on the development of a cytoplasmic component or complex capable of monitoring the time since initiation of germinal vesicle breakdown. Metabolic radiolabelling of oocytes which were able to respond to calcium ionophore, even though they had been prevented from undergoing normal chromosomal rearrangements, showed them to be synthesising a group of proteins known as the 35 kDa complex.
引用
收藏
页码:45 / 55
页数:11
相关论文
共 23 条
[1]  
Cascio S.M., Wassarman P.M., Program of early development in the mammal: post-transcriptional control of a class of proteins synthesized by mouse oocytes and early embryos, Dev. Biol., 89, pp. 397-408, (1982)
[2]  
Clarke H.J., Masui Y., The induction of reversible and irreversible chromosome decondensation by protein synthesis inhibition during meiotic maturation, Dev. Biol., 97, pp. 291-301, (1983)
[3]  
Clarke H.J., Rossant J., Masui Y., Suppression of chromosome condensation during meiotic maturation induces parthenogenic development of mouse oocytes, Development, 104, pp. 97-103, (1988)
[4]  
Gautier J., Norbury C., Lohka M., Nurse P., Mailer J., Purified maturation-promoting factor contains the product of a Xenopus homolog of the fission yeast cell cycle control gene cdc2+, Cell, 54, pp. 433-439, (1988)
[5]  
Gautier J., Minshull J., Lohka M.G., Glotzer M., Hunt T., Mailer J.L., Cyclin is a component of maturation promoting factor from Xenopus, Cell, 60, pp. 487-494, (1990)
[6]  
Howlett S.K., A set of proteins showing cell cycle dependent modifications in the early mouse embryo, Cell, 45, pp. 387-389, (1986)
[7]  
Hunt T., Under arrest in the cell cycle, Nature, 342, pp. 483-484, (1989)
[8]  
Kilmartin J., Wright B., Milstein C., Rat monoclonal anti-tubulin antibodies derived by using a new nonsecreting rat cell line, J. Cell Biol., 22, pp. 699-707, (1982)
[9]  
Kubiak J.Z., Mouse oocytes gradually develop the capacity for activation during the metaphase II arrest, Dev. Biol., 136, pp. 537-545, (1989)
[10]  
Kubiak J.Z., Weber M., Pennart H., Winston N.J., Maro B., The metaphase II arrest in mouse oocyte is controlled through microtubule dependent destruction of cyclin B in the presence of CSF, EMBO j., 12, pp. 3773-3778, (1993)