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Updated: Aug 19, 2026

Xenopus laevis as a Model to Identify Translation Impairment
Published on: September 27, 2015
Requirement of the c-mos protein kinase for murine meiotic maturation
Abstract:
Anti-sense mos oligonucleotides have been shown to block steps required for meiotic maturation of oocytes. In Xenopus oocytes, the block prevents germinal vesicle breakdown (GVBD), an early step in oocyte maturation. In mice the block induced by anti-sense mos occurs at a later step in oocyte maturation concerned with the first polar body emission. Here, we show that mouse oocyte maturation is blocked by introduction of anti-mos antibodies into immature functional oocytes. Antibodies that inhibit the mos kinase blocked GVBD. In contrast, anti-mos antibodies that permit the mos kinase to function do not block GVBD, but interfere with polar body formation. Antibodies pre-reacted with excess cognate peptide had no observable effects on maturation. These results indicate that the c-mos kinase function is required for activation of maturation-promoting factor (MPF) during meiosis. These findings are also consistent with our previous studies which show that the mos kinase directly phosphorylates cyclin B2, a component of MPF (Roy et al., 1990).
Insights
Anti-mos antibodies block mouse oocyte maturation by inhibiting mos kinase activity, preventing germinal vesicle breakdown (GVBD) and polar body formation. This highlights the essential role of mos kinase in meiotic maturation.
Area of Science:
- Cell Biology
- Developmental Biology
- Molecular Biology
Background:
- Anti-sense mos oligonucleotides inhibit oocyte maturation.
- In Xenopus, this block prevents germinal vesicle breakdown (GVBD).
- In mice, the block occurs later, affecting polar body emission.
Purpose of the Study:
- To investigate the role of mos kinase in mouse oocyte maturation.
- To determine the specific stage of maturation affected by mos kinase inhibition.
Main Methods:
- Introduction of anti-mos antibodies into immature mouse oocytes.
- Utilizing antibodies that either inhibit or permit mos kinase function.
- Observing effects on GVBD and polar body formation.
Main Results:
- Antibodies inhibiting mos kinase blocked GVBD.
- Antibodies allowing mos kinase function interfered with polar body formation.
- Pre-reacted antibodies showed no effect, confirming specificity.
Conclusions:
- c-mos kinase function is essential for maturation-promoting factor (MPF) activation during meiosis.
- Mos kinase directly phosphorylates cyclin B2, a key MPF component.
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