Fomproix N, Gébrane-Younès J, Hernandez-Verdun D
Institut Jacques Monod, Paris, France.
J Cell Sci. 1998 Feb;111 ( Pt 3):359-72. doi: 10.1242/jcs.111.3.359.
During mitosis some nuclear complexes are relocalized at the chromosome periphery and are then reintegrated into the re-forming nuclei in late telophase. To address questions concerning translocation from the chromosome periphery to nuclei, the dynamics of one nucleolar perichromosomal protein which is involved in the ribosomal RNA processing machinery, fibrillarin, was followed. In the same cells, the onset of the RNA polymerase I (RNA pol I) activity and translocation of fibrillarin were simultaneously investigated. In PtK1 cells, RNA pol I transcription was first detected at anaphase B. At the same mitotic stage, fibrillarin formed foci of increasing size around the chromosomes, these foci then gathered into prenucleolar bodies (PNBs) and later PNBs were targeted into the newly formed nucleoli. Electron microscopy studies enabled the visualization of the PNBs forming the dense fibrillar component (DFC) of new nucleoli. Anti-fibrillarin antibodies microinjected at different periods of mitosis blocked fibrillarin translocation at different steps, i.e. the formation of large foci, foci gathering in PNBs or PNB targeting into nucleoli, and thereby modified the ultrastructural organization of the nucleoli as well as of the PNBs. In addition, antibody-bound fibrillarin seemed localized with blocks of condensed chromatin in early G1 nuclei. It has been found that blocking fibrillarin translocation reduced or inhibited RNA pol I transcription. It is postulated that when translocation of proteins belonging to the processing machinery is inhibited or diminished, a negative feed-back effect is induced on nucleolar reassembly and transcriptional activity.
在有丝分裂期间,一些核复合物重新定位到染色体周边,然后在末期晚期重新整合到重新形成的细胞核中。为了解决有关从染色体周边向细胞核转运的问题,研究了一种参与核糖体RNA加工机制的核仁染色体周边蛋白原纤维蛋白的动态变化。在同一细胞中,同时研究了RNA聚合酶I(RNA pol I)活性的起始和原纤维蛋白的转运。在PtK1细胞中,RNA pol I转录首先在后期B期被检测到。在同一有丝分裂阶段,原纤维蛋白在染色体周围形成大小不断增加的聚集点,这些聚集点随后聚集成前核仁体(PNB),之后PNB靶向进入新形成的核仁。电子显微镜研究能够观察到形成新核仁致密纤维成分(DFC)的PNB。在有丝分裂的不同时期显微注射抗原纤维蛋白抗体,在不同步骤阻断原纤维蛋白的转运,即大聚集点的形成、聚集点聚集成PNB或PNB靶向进入核仁,从而改变了核仁以及PNB的超微结构组织。此外,抗体结合的原纤维蛋白似乎在G1早期细胞核中与浓缩染色质块共定位。已发现阻断原纤维蛋白的转运会降低或抑制RNA pol I转录。据推测,当属于加工机制的蛋白质转运受到抑制或减少时,会对核仁重新组装和转录活性产生负反馈效应。