Gavis E R, Lehmann R
Whitehead Institute for Biomedical Research, Howard Hughes Medical Institute, Department of Biology, Massachusetts Institute of Technology, Cambridge 02142.
Cell. 1992 Oct 16;71(2):301-13. doi: 10.1016/0092-8674(92)90358-j.
Anterior-posterior polarity of the Drosophila embryo is initiated during oogenesis through differential maternal RNA localization. The RNA of the anterior morphogen bicoid is localized to the anterior pole of the embryo, where bicoid protein controls head and thorax development. The RNA of the posterior morphogen nanos is localized to the posterior pole, where nanos protein is required for abdomen formation. Here we show that the nanos 3' untranslated region, like that of the bicoid RNA, is sufficient for RNA localization. We have used the bicoid RNA localization signal to mislocalize nanos, producing embryos with two sources of nanos protein. Such embryos form two abdomens with mirror image symmetry. Embryos with nanos RNA localized only to the anterior have greater nanos gene activity than embryos with nanos RNA localized posteriorly. We propose a role for RNA localization in regulating nanos activity.
果蝇胚胎的前后极性在卵子发生过程中通过母体RNA的差异定位而启动。前部形态发生素双尾的RNA定位于胚胎的前极,双尾蛋白在那里控制头部和胸部的发育。后部形态发生素纳米的RNA定位于后极,腹部形成需要纳米蛋白。我们在此表明,纳米的3'非翻译区与双尾RNA的3'非翻译区一样,足以实现RNA定位。我们利用双尾RNA定位信号使纳米异位定位,产生具有两个纳米蛋白来源的胚胎。这样的胚胎形成两个呈镜像对称的腹部。纳米RNA仅定位于前部的胚胎比纳米RNA定位于后部的胚胎具有更高的纳米基因活性。我们提出RNA定位在调节纳米活性中发挥作用。