Gavis E R, Lunsford L, Bergsten S E, Lehmann R
Whitehead Institute for Biomedical Research, Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge 02142, USA.
Development. 1996 Sep;122(9):2791-800. doi: 10.1242/dev.122.9.2791.
Correct formation of the Drosophila body plan requires restriction of nanos activity to the posterior of the embryo. Spatial regulation of nanos is achieved by a combination of RNA localization and localization-dependent translation such that only posteriorly localized nanos RNA is translated. Cis-acting sequences that mediate both RNA localization and translational regulation lie within the nanos 3' untranslated region. We have identified a discrete translational control element within the nanos 3' untranslated region that acts independently of the localization signal to mediate translational repression of unlocalized nanos RNA. Both the translational regulatory function of the nanos 3'UTR and the sequence of the translational control element are conserved between D. melanogaster and D. virilis. Furthermore, we show that the RNA helicase Vasa, which is required for nanos RNA localization, also plays a critical role in promoting nanos translation. Our results specifically exclude models for translational regulation of nanos that rely on changes in polyadenylation.
果蝇身体模式的正确形成需要将纳米斯(nanos)活性限制在胚胎的后部。纳米斯的空间调控是通过RNA定位和定位依赖性翻译的组合来实现的,使得只有位于后部的纳米斯RNA被翻译。介导RNA定位和翻译调控的顺式作用序列位于纳米斯3'非翻译区内。我们在纳米斯3'非翻译区内鉴定出一个离散的翻译控制元件,它独立于定位信号起作用,介导未定位的纳米斯RNA的翻译抑制。纳米斯3'UTR的翻译调控功能和翻译控制元件的序列在黑腹果蝇和拟果蝇之间是保守的。此外,我们表明,纳米斯RNA定位所需的RNA解旋酶瓦萨(Vasa)在促进纳米斯翻译中也起着关键作用。我们的结果特别排除了依赖于多聚腺苷酸化变化的纳米斯翻译调控模型。