MAP激酶和p34cdc2/cyclin B在非洲爪蟾卵母细胞减数分裂成熟过程中的激活。

A Palmer, A R Nebreda
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引用次数: 56

摘要

孕激素刺激可诱导g2阻滞爪蟾卵母细胞进入减数分裂m期。这一过程被称为减数分裂成熟,需要激活p34cdc2/cyclin B复合物(pre-MPF),这是由储存在卵母细胞中的特异性母体mrna的预先翻译带来的。其中一种mrna编码蛋白激酶Mos,该蛋白激酶在卵母细胞成熟中起重要作用,很可能是由于其激活MAP激酶(MAPK)的能力。在这里,我们回顾了我们目前对Mos/MAPK信号通路的了解,以及最近发现的MAPK激活的p90rsk与p34cdc2抑制激酶Myt1之间的联系。我们还讨论了一种涉及蛋白激酶Plx1并导致磷酸酶Cdc25激活的途径,以及可能在卵母细胞成熟中起作用的p34cdc2/cyclin B活性的其他调节因子。
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The activation of MAP kinase and p34cdc2/cyclin B during the meiotic maturation of Xenopus oocytes.

G2-arrested Xenopus oocytes are induced to enter M-phase of meiosis by progesterone stimulation. This process, known as meiotic maturation, requires the activation of p34cdc2/cyclin B complexes (pre-MPF) which is brought about by the prior translation of specific maternal mRNAs stored in the oocyte. One of these mRNAs encodes for the protein kinase Mos which has an essential role in oocyte maturation, most likely due to its ability to activate MAP kinase (MAPK). Here we review our current knowledge on the Mos/MAPK signalling pathway and a recently found connection between MAPK-activated p90rsk and the p34cdc2 inhibitory kinase Myt1. We also discuss a pathway that involves the protein kinase Plx1 and leads to the activation of the phosphatase Cdc25, as well as other regulators of p34cdc2/cyclin B activity which may have a role in oocyte maturation.

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