Gunkel N, Yano T, Markussen F H, Olsen L C, Ephrussi A
European Molecular Biology Laboratory (EMBL), Developmental Biology Programme, 69117 Heidelberg, Germany.
Genes Dev. 1998 Jun 1;12(11):1652-64. doi: 10.1101/gad.12.11.1652.
The precise restriction of proteins to specific domains within a cell plays an important role in early development and differentiation. An efficient way to localize and concentrate proteins is by localization of mRNA in a translationally repressed state, followed by activation of translation when the mRNA reaches its destination. A central issue is how localized mRNAs are derepressed. In this study we demonstrate that, when oskar mRNA reaches the posterior pole of the Drosophila oocyte, its translation is derepressed by an active process that requires a specific element in the 5' region of the mRNA. We demonstrate that this novel type of element is a translational derepressor element, whose functional interaction with the previously identified repressor region in the oskar 3' UTR is required for activation of oskar mRNA translation at the posterior pole. The derepressor element only functions at the posterior pole, suggesting that a locally restricted interaction between trans-acting factors and the derepressor element may be the link between mRNA localization and translational activation. We also show specific interaction of two proteins with the oskar mRNA 5' region; one of these also recognizes the 3' repressor element. We discuss the possible involvement of these factors as well as known genes in the process of localization-dependent translation.
蛋白质精确地定位于细胞内的特定区域,这在早期发育和分化过程中起着重要作用。一种定位和浓缩蛋白质的有效方法是将处于翻译抑制状态的mRNA进行定位,然后当mRNA到达其目的地时激活翻译。一个核心问题是定位的mRNA如何解除抑制。在本研究中,我们证明,当osk基因mRNA到达果蝇卵母细胞的后极时,其翻译通过一个活跃的过程被解除抑制,该过程需要mRNA 5'区域中的一个特定元件。我们证明这种新型元件是一种翻译去抑制元件,其与osk基因3'UTR中先前鉴定的抑制区域的功能相互作用是osk基因mRNA在后极翻译激活所必需的。该去抑制元件仅在后极发挥作用,这表明反式作用因子与去抑制元件之间局部受限的相互作用可能是mRNA定位与翻译激活之间的联系。我们还展示了两种蛋白质与osk基因mRNA 5'区域的特异性相互作用;其中一种蛋白质也能识别3'抑制元件。我们讨论了这些因子以及已知基因在定位依赖性翻译过程中的可能作用。