Click here to close
Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly.
We suggest using a current version of Chrome,
FireFox, or Safari.
Cycling of intracellular pH during cell division of Xenopus embryos is a cytoplasmic activity depending on protein synthesis and phosphorylation.
Grandin N
,
Charbonneau M
.
Abstract
In Xenopus embryos, the successive and rapid cell divisions that follow fertilization are accompanied by periodic oscillations of intracellular pH (pHi). Cycling of pHi occurs in phase with several other oscillatory activities, namely nuclear divisions, M phase-promoting factor (MPF) activity, and surface contraction waves (SCWs). We report that treatments that abolish cycling of MPF activity and the SCWs also suppress the pHi oscillations, whereas those that block cell division without affecting neither MPF activity nor the SCWs do not suppress the pHi oscillations. Experiments on enucleated oocytes, matured in vitro and activated, demonstrated that the activity governing the rhythmicity of the pHi oscillations resided in the cytoplasm of the oocyte. In this respect, the activity responsible for the pHi oscillations was different from that which drives the SCWs, which necessitated the presence of the oocytegerminal vesicle (Ohsumi et al., 1986), but more closely resembled MPF activity that did not require the presence of the oocytegerminal vesicle (Dabauvalle et al., 1988). In mature eggs enucleated at the time of egg activation, the pHi oscillations were similar to those in control nucleated eggs, whereas the period between two peaks of SCWs was 35-60 min vs. 20-35 min in nucleated control eggs. Previous studies had shown that the periodicity of SCWs was larger in anucleate egg fragments than in their nucleate counterparts (Sakai and Kubota, 1981), the difference being on the order of 6-15 min (Shinagawa, 1983). However, in these previous studies, enucleation was performed 30-50 min after fertilization. Our results clearly demonstrate that the periodicity of the SCWs is lengthened when the interval between egg activation and enucleation is shortened, thereby providing an easier way to assess the nuclear dependency of the SCWs. Finally, the various possibilities concerning the role of pHi cycling during cell division are discussed.
Ammann,
Neutral carrier based hydrogen ion selective microelectrode for extra- and intracellular studies.
1981, Pubmed
Ammann,
Neutral carrier based hydrogen ion selective microelectrode for extra- and intracellular studies.
1981,
Pubmed
Arion,
cdc2 is a component of the M phase-specific histone H1 kinase: evidence for identity with MPF.
1988,
Pubmed
,
Xenbase
Arion,
M-phase-specific protein kinase from mitotic sea urchin eggs: cyclic activation depends on protein synthesis and phosphorylation but does not require DNA or RNA synthesis.
1989,
Pubmed
Dabauvalle,
Role of nuclear material in the early cell cycle of Xenopus embryos.
1988,
Pubmed
,
Xenbase
Dreyer,
Differential accumulation of oocyte nuclear proteins by embryonic nuclei of Xenopus.
1987,
Pubmed
,
Xenbase
Dumont,
Oogenesis in Xenopus laevis (Daudin). I. Stages of oocyte development in laboratory maintained animals.
1972,
Pubmed
,
Xenbase
Felix,
A post-ribosomal supernatant from activated Xenopus eggs that displays post-translationally regulated oscillation of its cdc2+ mitotic kinase activity.
1989,
Pubmed
,
Xenbase
Ford,
A method for enucleating oocytes of Xenopus laevis.
1977,
Pubmed
,
Xenbase
Gerhart,
Cell cycle dynamics of an M-phase-specific cytoplasmic factor in Xenopus laevis oocytes and eggs.
1984,
Pubmed
,
Xenbase
Grandin,
Intracellular pH and the increase in protein synthesis accompanying activation of Xenopus eggs.
1989,
Pubmed
,
Xenbase
Hara,
A cytoplasmic clock with the same period as the division cycle in Xenopus eggs.
1980,
Pubmed
,
Xenbase
Kimelman,
The events of the midblastula transition in Xenopus are regulated by changes in the cell cycle.
1987,
Pubmed
,
Xenbase
Labbe,
Purification of MPF from starfish: identification as the H1 histone kinase p34cdc2 and a possible mechanism for its periodic activation.
1989,
Pubmed
,
Xenbase
Lee,
Observations on intracellular pH during cleavage of eggs of Xenopus laevis.
1981,
Pubmed
,
Xenbase
Masui,
Cytoplasmic control of nuclear behavior during meiotic maturation of frog oocytes.
1971,
Pubmed
Neant,
6-Dimethylaminopurine blocks starfish oocyte maturation by inhibiting a relevant protein kinase activity.
1988,
Pubmed
Ohsumi,
Periodic changes in the rigidity of activated anuran eggs depend on germinal vesicle materials.
1986,
Pubmed
,
Xenbase
Rebhun,
Cleavage inhibition in marine eggs by puromycin and 6-dimethylaminopurine.
1973,
Pubmed
Richter,
SDS-polyacrylamide gel electrophoresis of isolated cortices of Xenopus laevis eggs.
1980,
Pubmed
,
Xenbase
Sawai,
Cyclic changes in the cortical layer of non-nucleated fragments of the newt's egg.
1979,
Pubmed
Shinagawa,
The interval of the cytoplasmic cycle observed in non-nucleate egg fragments is longer than that of the cleavage cycle in normal eggs of Xenopus laevis.
1983,
Pubmed
,
Xenbase
Wallace,
Protein incorporation by isolated amphibian oocytes. 3. Optimum incubation conditions.
1973,
Pubmed
,
Xenbase
Webb,
Direct measurement of intracellular pH changes in Xenopus eggs at fertilization and cleavage.
1981,
Pubmed
,
Xenbase