Eckner R, Ellmeier W, Birnstiel M L
Research Institute of Molecular Pathology, Vienna, Austria.
EMBO J. 1991 Nov;10(11):3513-22. doi: 10.1002/j.1460-2075.1991.tb04915.x.
We have analysed nucleocytoplasmic export of mRNAs in primate cells with the aim of identifying signals promoting RNA transport. Our results demonstrate that sequences directing either histone mRNA 3' processing or cleavage/polyadenylation of mRNA stimulate nucleocytoplasmic RNA transport. To elucidate the nature of this stimulation, we engineered test gene transcripts which could obtain a mature histone 3' end by the RNA cleaving activity of a cis-acting ribozyme, thus circumventing the cellular 3' end processing machinery. However, such transcripts were found to be transport deficient and accumulated in the nuclear compartment. Our experiments provide genetic evidence that there is a linkage between 3' end formation and the export of RNA transcripts from the nucleus. Analysis of a similar series of histone mRNAs in which the mature 3' end was generated by means of ribozyme cleavage led to the discovery of a second export mechanism which relies on features specific for mature histone RNA and which can be uncoupled from the cellular processing machinery. The presence of histone mRNA sequences and of the highly conserved histone hairpin structure, positioned close to the 3' terminus, are critical determinants for this export mechanism.
我们分析了灵长类细胞中mRNA的核质输出,目的是识别促进RNA转运的信号。我们的结果表明,指导组蛋白mRNA 3'加工或mRNA切割/聚腺苷酸化的序列会刺激核质RNA转运。为了阐明这种刺激的本质,我们构建了测试基因转录本,这些转录本可以通过顺式作用核酶的RNA切割活性获得成熟的组蛋白3'末端,从而避开细胞的3'末端加工机制。然而,发现这类转录本存在转运缺陷,并在核区室中积累。我们的实验提供了遗传学证据,表明3'末端形成与RNA转录本从细胞核输出之间存在联系。对一系列类似的组蛋白mRNA进行分析,其中成熟的3'末端是通过核酶切割产生的,这导致发现了第二种输出机制,该机制依赖于成熟组蛋白RNA特有的特征,并且可以与细胞加工机制分离。靠近3'末端的组蛋白mRNA序列和高度保守的组蛋白发夹结构的存在是这种输出机制的关键决定因素。