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首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >Characterization of Ribosomal S6 Protein Kinase p90rsk During Meiotic Maturation and Fertilization in Pig Oocytes: Mitogen-Activated Protein Kinase-Associated Activation and Localization.
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Characterization of Ribosomal S6 Protein Kinase p90rsk During Meiotic Maturation and Fertilization in Pig Oocytes: Mitogen-Activated Protein Kinase-Associated Activation and Localization.

机译:猪卵母细胞减数分裂成熟和受精过程中核糖体S6蛋白激酶p90rsk的特征:丝裂原活化蛋白激酶相关的活化和定位。

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摘要

Mitogen-activated protein kinase (MAPK) becomes activated during the meiotic maturation of pig oocytes, but its physiological substrate is unknown. The 90-kDa ribosome S6 protein kinase (p90rsk) is the best known MAPK substrate in Xenopus and mouse oocytes. The present study was designed to investigate the expression, phosphorylation, subcellular localization, and possible roles of p90rsk in porcine oocytes during meiotic maturation, fertilization, and parthenogenetic activation. This kinase was partially phosphorylated in oocytes at germinal vesicle (GV) stage through a MAPK-independent mechanism, but its full phosphorylation is dependent on MAPK activity. After fertilization or electrical activation, p90rsk was dephosphorylated shortly before pronucleus formation, which coincided with the inactivation of MAPK. A protein phosphatase inhibitor, okadaic acid, accelerated the phosphorylation of p90rsk during meiotic maturation and induced its rephosphorylation in activated eggs. MAPK kinase (MAPKK or MEK) inhibitor U0126 inhibited the activation of MAPK and p90rsk in both cumulus-enclosed and denuded pig oocytes, but prevented GV breakdown (GVBD) only in cumulus-enclosed oocytes. Active MAPK and p90rsk were detected in pig cumulus cells, and U0126 induced their dephosphorylation. In meiosis II arrested eggs, U0126 led to the inactivation of MAPK and p90rsk, as well as the interphase transition of the eggs. P90rsk was distributed evenly in GV oocytes, but it accumulated in the nucleus before GVBD. It was localized to the meiotic spindle after GVBD and concentrated in the spindle mid zone during emission of the polar bodies. All these results suggest that p90rsk is downstream of MAPK and plays functional roles in the regulation of nuclear status and microtubule organization. Although MAPK and p90rsk activity are not essential for the spontaneous meiotic resumption in denuded oocytes, activation of this cascade in cumulus cells is indispensable for the gonadotropin-induced meiotic resumption of pig oocytes.
机译:丝裂原激活的蛋白激酶(MAPK)在猪卵母细胞减数分裂成熟期间被激活,但其生理底物尚不清楚。 90 kDa核糖体S6蛋白激酶(p90rsk)是非洲爪蟾和小鼠卵母细胞中最著名的MAPK底物。本研究旨在研究减数分裂成熟,受精和孤雌生殖激活过程中p90rsk在猪卵母细胞中的表达,磷酸化,亚细胞定位以及可能的作用。该激酶通过不依赖MAPK的机制在生小泡(GV)阶段在卵母细胞中被部分磷酸化,但其完全磷酸化依赖于MAPK活性。受精或电激活后,p90rsk在原核形成前不久被去磷酸化,这与MAPK失活相吻合。蛋白磷酸酶抑制剂冈田酸可在减数分裂成熟过程中加速p90rsk的磷酸化,并在活化的卵中诱导其重新磷酸化。 MAPK激酶(MAPKK或MEK)抑制剂U0126抑制卵母细胞包埋和裸露的卵母细胞中MAPK和p90rsk的活化,但仅在卵母细胞包埋的卵母细胞中阻止GV分解(GVBD)。在猪卵丘细胞中检测到活跃的MAPK和p90rsk,U0126诱导了它们的去磷酸化。在减数分裂II捕获的卵中,U0126导致MAPK和p90rsk失活,以及卵的相变。 P90rsk在GV卵母细胞中均匀分布,但在GVBD前聚集在细胞核中。它在GVBD之后定位于减数分裂纺锤体,并在发射极体时集中在纺锤体中间区域。所有这些结果表明,p90rsk位于MAPK的下游,并在调节核状态和微管组织中发挥功能性作用。尽管MAPK和p90rsk活性对于裸露的卵母细胞自发减数分裂恢复不是必需的,但对于促性腺激素诱导的猪卵母细胞减数分裂恢复,卵丘细胞中级联的激活是必不可少的。

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