Changes in maturation‐promoting activity in the cytoplasm of pig oocytes throughout maturation
- 1 October 1991
- journal article
- research article
- Published by Wiley in Molecular Reproduction and Development
- Vol. 30 (2) , 119-125
- https://doi.org/10.1002/mrd.1080300208
Abstract
Maturation‐promoting factor (MPF) was examined in maturing pig oocytes by electrofusing them with germinal vesicle (GV) oocytes. Oocytes containing high levels of MPF (MI or MII stages) induced the breakdown of the GV introduced by fusion and the formation of the metaphase plate in 1 hr. A similar effect was seen when two or three GV oocytes were fused with a MII oocyte and then incubated for 1 hr in the presence of cycloheximide (a specific protein synthesis inhibitor), indicating that high levels of preformed MPF are present at the metaphase stage. During the maturation in vitro of cumulus‐enclosed oocytes, a first sharp rise in MPF was seen between 26 and 29 hr of culture (MI stage); MPF declined after 2 hr (AI‐TI stages) and again reached high levels at 35 hr, where it remained for the rest of maturation. Denuded oocytes showed a similar behavior, but MPF appeared 9 hr earlier and the rise, due to the asynchronous maturation of these oocytes, was not as sharp as in cumulus enclosed oocytes. Cycloheximide was used to study protein synthesis requirements for oocyte maturation. Intact GV were observed after 44 hr of culture when cycloheximide was added at 26 hr or earlier, and chromosome decondensation and pronuclear formation were observed when the drug was added at 32 hr. Transcriptional requirements were investigated by treating the oocytes with α‐amanitin, an RNA polymerase inhibitor. This drug could completely inhibit the maturation of cumulus‐enclosed oocytes, but this was a somatic cell‐mediated effect since denuded oocytes were insensitive to this treatment. Enucleated oocytes exhibited an increase in MPF after 24 hr of culture, and low levels of this factor were seen after 40 h of maturation. These data indicate that both rises in MPF require active protein synthesis, whereas transcription is not necessary for the resumption of meiotic cycle. Nuclear activity may be required for the second rise in MPF.Keywords
This publication has 26 references indexed in Scilit:
- Purified maturation promoting factor phosphorylates pp60c-src at the sites phosphorylated during fibroblast mitosisCell, 1989
- Inhibition by dibutyryl cyclic AMP of the transition to metaphase of mouse oocyte nuclei and its reversal by cell fusion to metaphase oocytesDevelopmental Biology, 1985
- Effect of follicle cells on the maturation and developmental competence of ovine oocytes matured outside the follicleGamete Research, 1984
- Generality of the action of various maturation-promoting factorsExperimental Cell Research, 1982
- Evidence for the involvement of H1 histone phosphorylation in chromosome condensationNature, 1980
- Induction of maturation in small oocytes from sexually immature mice by fusion with meiotic or mitotic cellsExperimental Cell Research, 1978
- Qualitative patterns of protein synthesis in the mouse oocyteJournal of Experimental Zoology, 1976
- A cytostatic factor in amphibian oocytes: Its extraction and partial characterizationJournal of Experimental Zoology, 1974
- The interaction of steroids with Rana pipiens oocytes in the induction of maturationDevelopmental Biology, 1971
- MEIOSIS AND INHIBITION OF OVULATION IN MOUSE EGGS TREATED WITH ACTINOMYCIN DThe Journal of cell biology, 1969