Piccioni Federica, Zappavigna Vincenzo, Verrotti Arturo C
CEINGE-Biotecnologie Avanzate, Via Comunale Margherita 482, 80145 Naples, Italy.
C R Biol. 2005 Oct-Nov;328(10-11):863-81. doi: 10.1016/j.crvi.2005.05.006. Epub 2005 Jun 8.
Metazoans rely on the regulated translation of select maternal mRNAs to control oocyte maturation and the initial stages of embryogenesis. These transcripts usually remain silent until their translation is temporally and spatially required during early development. Different translational regulatory mechanisms, varying from cytoplasmic polyadenylation to localization of maternal mRNAs, have evolved to assure coordinated initiation of development. A common feature of these mechanisms is that they share a few key trans-acting factors. Increasing evidence suggest that ubiquitous conserved mRNA-binding factors, including the eukaryotic translation initiation factor 4E (eIF4E) and the cytoplasmic polyadenylation element binding protein (CPEB), interact with cell-specific molecules to accomplish the correct level of translational activity necessary for normal development. Here we review how capping and polyadenylation of mRNAs modulate interaction with multiple regulatory factors, thus controlling translation during oogenesis and early development.
后生动物依靠对特定母体mRNA的调控翻译来控制卵母细胞成熟和胚胎发育的初始阶段。这些转录本通常保持沉默,直到在早期发育过程中其翻译在时间和空间上被需要。从细胞质聚腺苷酸化到母体mRNA定位等不同的翻译调控机制已经进化出来,以确保发育的协调启动。这些机制的一个共同特征是它们共享一些关键的反式作用因子。越来越多的证据表明,包括真核翻译起始因子4E(eIF4E)和细胞质聚腺苷酸化元件结合蛋白(CPEB)在内的普遍保守的mRNA结合因子,与细胞特异性分子相互作用,以实现正常发育所需的正确水平的翻译活性。在这里,我们综述了mRNA的加帽和聚腺苷酸化如何调节与多种调控因子的相互作用,从而在卵子发生和早期发育过程中控制翻译。