首页> 外文期刊>The Journal of Reproduction and Development >Inhibition of Mitogen Activated Protein Kinase Activity Induces Parthenogenetic Activation and Increases Cyclin B Accumulation during Porcine Oocyte Maturation
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Inhibition of Mitogen Activated Protein Kinase Activity Induces Parthenogenetic Activation and Increases Cyclin B Accumulation during Porcine Oocyte Maturation

机译:猪卵母细胞成熟过程中丝裂原活化蛋白激酶活性的抑制诱导孤雌激活并增加细胞周期蛋白B的积累。

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摘要

The inhibition of mitogen activated protein kinase (MAPK) activation during porcine oocyte maturation leads to decreased maturation promoting factor (MPF) activity and to the induction of parthenogenetic activation. In the present study, in order to analyze the mechanism underlying the suppression of MPF activity in MAPK-inhibited porcine oocytes, we injected mRNA of SASA-MEK, a dominant negative MAPK kinase, or antisense RNA of c-mos, a MAPK kinase kinase, into immature porcine oocyte cytoplasm. Theinjection of SASA-MEK mRNA or c-mos antisense RNA inhibited the MAPK activity partially or completely, respectively, decreased the MPF activity slightly or significantly, respectively, and induced parthenogenetic activation in 17.1% or 96.6% of mature oocytes, respectively, although no parthenogenetic activation was observed in the control oocytes. Immunoblotting experiments revealed that cyclin B accumulation in these MAPK-suppressed porcine oocytes was increased significantly after 50 h of culture and that a considerable amount of MPF was converted into inactive pre-MPF by hyperphosphorylation. These results indicate that the inhibition of MAPK activity in porcine oocytes did not promote cyclin B degradation but rather suppressed it; also the decrease in MPF activity in MAPK-suppressed porcine oocytes correlated with the conversion of active MPF into inactive pre-MPF.
机译:猪卵母细胞成熟过程中对促分裂原活化蛋白激酶(MAPK)激活的抑制导致成熟促进因子(MPF)活性降低,并诱导孤雌生殖激活。在本研究中,为了分析抑制MAPK抑制的猪卵母细胞中MPF活性抑制的机制,我们注射了SASA-MEK mRNA(一种显性负MAPK激酶)或c-mos反义RNA(一种MAPK激酶激酶) ,进入未成熟的猪卵母细胞的细胞质。注射SASA-MEK mRNA或c-mos反义RNA分别部分或完全抑制MAPK活性,分别轻微或显着降低MPF活性,并分别诱导17.1%或96.6%的成熟卵母细胞孤雌生殖活化,尽管没有。在对照卵母细胞中观察到孤雌生殖激活。免疫印迹实验表明,培养50 h后,这些受MAPK抑制的猪卵母细胞中细胞周期蛋白B的积累显着增加,并且大量的MPF通过高磷酸化转化为非活性的MPF前体。这些结果表明,抑制猪卵母细胞中MAPK活性不会促进细胞周期蛋白B的降解,反而会抑制细胞周期蛋白B的降解。 MAPK抑制的猪卵母细胞中MPF活性的降低也与活性MPF转化为无活性的MPF前相关。

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