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Analysis of mRNA Associated Factors During Bovine Oocyte Maturation and Early Embryonic Development

机译:牛卵母细胞成熟和早期胚胎发育过程中的mRNA相关因素分析

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Regulation of gene expression at the translational level is particularly essential during developmental periods, when transcription is impaired. According to the closed-loop model of translational initiation, we have analyzed components of the 5'-mRNA cap-binding complex eIF4F (eIF4E, eIF4G, eIF4A), the eIF4E repressor 4E-BP1, and 3'-mRNA poly-(A) tail-associated proteins (PABP1 and 3, PAIP1 and 2, CPEB1, Maskin) during in vitro maturation of bovine oocytes and early embryonic development up to the 16-cell stage. Furthermore, we have elucidated the activity of distinct kinases which are potentially involved in their phosphorylation. Major phosphorylation of specific target sequences of PKA, PKB, PKC, CDKs, ATM/ATR, and MAPK were observed in M II stage oocytes. Furthermore, main changes in the abundance and/or phosphorylation of distinct mRNA-binding factors occur at the transition from M II stage oocytes to 2-cell embryos. In conclusion, the results indicate that, at the transition from oocyte to embryonic development, translational initiation is regulated by striking differences in the abundance and/or phosphorylation of 5'-end and 3'-end mRNA associated factors, mainly the poly-(A) bindings proteins PABP1 and 3, their repressor PAIP2 and a Maskin-like protein with distinct eIF4E-binding properties which prevents eIF4E/cap binding and eIF4F formation in vitro. Nevertheless, from the M II stage to 16-cell embryos a substantial amount of eIF4E and, to a lesser extent, of eIF4G was precipitated by (7)m-GTP-Separose indicating eIF4F complex formation. Therefore, it is likely that in general the reduction in PABP1 and 3 abundance represses overall translation during early embryonic development.
机译:在转录水平受损的发育阶段,在翻译水平上调节基因表达尤为重要。根据翻译起始的闭环模型,我们分析了5'-mRNA帽结合复合物eIF4F(eIF4E,eIF4G,eIF4A),eIF4E阻遏物4E-BP1和3'-mRNA poly-(A )牛卵母细胞的体外成熟和直至16细胞阶段的早期胚胎发育过程中的尾巴相关蛋白(PABP1和3,PAIP1和2,CPEB1和Maskin)。此外,我们阐明了可能参与其磷酸化的独特激酶的活性。在M II期卵母细胞中观察到PKA,PKB,PKC,CDK,ATM / ATR和MAPK的特定靶序列的主要磷酸化。此外,不同的mRNA结合因子的丰度和/或磷酸化的主要变化发生在从M II期卵母细胞到2细胞胚胎的过渡中。总之,结果表明,在从卵母细胞到胚胎发育的过渡过程中,翻译起始受5'-端和3'-端mRNA相关因子(主要是聚-( A)结合蛋白PABP1和3,其阻遏物PAIP2和具有独特eIF4E结合特性的Maskin样蛋白,从而阻止eIF4E /帽结合和eIF4F体外形成。然而,从M II阶段到16细胞胚胎,大量的eIF4E和较小程度的eIF4G被(7)m-GTP-琼脂糖沉淀,表明形成eIF4F复合体。因此,一般来说,PABP1和3丰度的降低可能会抑制早期胚胎发育期间的整体翻译。

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