Wharton R P, Sonoda J, Lee T, Patterson M, Murata Y
Howard Hughes Medical Institute, Department of Genetics, Duke University Medical Center, Durham, North Carolina 27710, USA.
Mol Cell. 1998 May;1(6):863-72. doi: 10.1016/s1097-2765(00)80085-4.
Posterior patterning in the Drosophila embryo requires the action of Nanos (Nos) and Pumilio (Pum), which collaborate to regulate the translation of maternal hunchback (hb) mRNA. Previous work demonstrated that Pum recognizes sites in the 3' UTR of hb mRNA. In this report, we first define the RNA-binding domain of Pum and then show that residues essential for translational repression are embedded within this domain. We also show that Nos and Pum can repress cap-independent translation from an internal ribosome entry site (IRES) in vivo, suggesting that they act downstream of the initial steps of normal, cap-dependent translation.
果蝇胚胎的后部模式形成需要Nanos(Nos)和Pumilio(Pum)的作用,它们协同调节母体驼背(hb)mRNA的翻译。先前的研究表明,Pum识别hb mRNA 3'UTR中的位点。在本报告中,我们首先定义了Pum的RNA结合结构域,然后表明翻译抑制所必需的残基嵌入在该结构域内。我们还表明,Nos和Pum可以在体内从内部核糖体进入位点(IRES)抑制不依赖帽的翻译,这表明它们在正常的依赖帽的翻译的初始步骤下游起作用。