Guddat U, Bakken A H, Pieler T
Max-Planck-Institut für Molekulare Genetik, Otto-Warburg-Laboratorium, Berlin, Federal Republic of Germany.
Cell. 1990 Feb 23;60(4):619-28. doi: 10.1016/0092-8674(90)90665-2.
We have analyzed RNP formation and nucleocytoplasmic migration of 5S RNA and 5S RNA variants transcribed from microinjected genes in Xenopus oocytes. Using antisera against three different proteins we find that newly transcribed nuclear 5S rRNA transiently interacts with La antigen. The La protein is then replaced by either ribosomal protein L5 or the 5S gene-specific transcription factor IIIA (TFIIIA), and each of these two RNPs migrates out of the nucleus and accumulates in the cytoplasm. RNA molecules that are impaired in their ability to interact with L5 and TFIIIA are retained in the nucleus. Thus, L5 and TFIIIA define a new functional class of proteins involved in the nuclear export of RNA. In addition, we show that RNP migration depletes the nucleus of TFIIIA, resulting in a loss of transcription competence for newly injected 5S rRNA genes.
我们分析了非洲爪蟾卵母细胞中从显微注射基因转录而来的5S RNA和5S RNA变体的核糖核蛋白(RNP)形成及核质迁移情况。使用针对三种不同蛋白质的抗血清,我们发现新转录的核5S rRNA会与La抗原短暂相互作用。然后La蛋白会被核糖体蛋白L5或5S基因特异性转录因子IIIA(TFIIIA)取代,这两种核糖核蛋白中的每一种都会从细胞核中迁移出来并积聚在细胞质中。与L5和TFIIIA相互作用能力受损的RNA分子会保留在细胞核中。因此,L5和TFIIIA定义了一类参与RNA核输出的新功能蛋白。此外,我们表明RNP迁移会耗尽细胞核中的TFIIIA,导致新注射的5S rRNA基因失去转录能力。