Lasko P, Cho P, Poulin F, Sonenberg N
Department of Biology, McGill University, 1205 Avenue Docteur Penfield, Montréal, QC, Canada H3A 1B1.
Biochem Soc Trans. 2005 Dec;33(Pt 6):1544-6. doi: 10.1042/BST0331544.
Translational control is a key genetic regulatory mechanism underlying the initial establishment of the major spatial axes of the Drosophila embryo. Many translational control mechanisms target eIF4E (eukaryotic initiation factor 4E), an initiation factor that recognizes the 5'-cap structure of the mRNA. Cap recognition by eIF4E, in complex with eIF4G, is essential for recruitment of the mRNA to the small ribosomal subunit. One established mechanism for repressing translation involves eIF4E-binding proteins, which competitively inhibit the eIF4E-eIF4G interaction. Our group has uncovered a novel mechanism for repression in which an eIF4E cognate protein called d4EHP, which cannot bind eIF4G, binds to the 5'-cap structure of cad mRNA thus rendering it translationally inactive. These two related, but distinct, mechanisms are discussed and contrasted in this review.
翻译控制是果蝇胚胎主要空间轴初始建立背后的关键基因调控机制。许多翻译控制机制靶向真核生物起始因子4E(eIF4E),这是一种识别mRNA 5'端帽结构的起始因子。eIF4E与eIF4G形成复合物识别帽结构,对于将mRNA招募到小核糖体亚基至关重要。一种已确立的抑制翻译的机制涉及eIF4E结合蛋白,其竞争性抑制eIF4E-eIF4G相互作用。我们的研究小组发现了一种新的抑制机制,其中一种名为d4EHP的eIF4E同源蛋白不能结合eIF4G,它与cad mRNA的5'端帽结构结合,从而使其翻译失活。在这篇综述中讨论并对比了这两种相关但不同的机制。