Huang S, Deerinck T J, Ellisman M H, Spector D L
Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 11724, USA.
J Cell Biol. 1997 Jun 2;137(5):965-74. doi: 10.1083/jcb.137.5.965.
The perinucleolar compartment (PNC) is a unique nuclear structure preferentially localized at the periphery of the nucleolus. Several small RNAs transcribed by RNA polymerase III (e.g., the Y RNAs, MRP RNA, and RNase P H1 RNA) and the polypyrimidine tract binding protein (PTB; hnRNP I) have thus far been identified in the PNC (Ghetti, A., S. PinolRoma, W.M. Michael, C. Morandi, and G. Dreyfuss. 1992. Nucleic Acids Res. 20:3671-3678; Matera, A.G., M.R. Frey, K. Margelot, and S.L. Wolin. 1995. J. Cell Biol. 129:1181-1193; Lee, B., A.G. Matera, D.C. Ward, and J. Craft. 1996. Proc. Natl. Acad. Sci. USA. 93: 11471-11476). In this report, we have further characterized this structure in both fixed and living cells. Detection of the PNC in a large number of human cancer and normal cells showed that PNCs are much more prevalent in cancer cells. Analysis through the cell cycle using immunolabeling with a monoclonal antibody, SH54, specifically recognizing PTB, demonstrated that the PNC dissociates at the beginning of mitosis and reforms at late telophase in the daughter nuclei. To visualize the PNC in living cells, a fusion protein between PTB and green fluorescent protein (GFP) was generated. Time lapse studies revealed that the size and shape of the PNC is dynamic over time. In addition, electron microscopic examination in optimally fixed cells revealed that the PNC is composed of multiple strands, each measuring approximately 80-180 nm diam. Some of the strands are in direct contact with the surface of the nucleolus. Furthermore, analysis of the sequence requirement for targeting PTB to the PNC using a series of deletion mutants of the GFP-PTB fusion protein showed that at least three RRMs at either the COOH or NH2 terminus are required for the fusion protein to be targeted to the PNC. This finding suggests that RNA binding may be necessary for PTB to be localized in the PNC.
核仁周边区(PNC)是一种独特的核结构,优先定位于核仁周边。到目前为止,在核仁周边区已鉴定出几种由RNA聚合酶III转录的小RNA(如Y RNA、MRP RNA和核糖核酸酶P H1 RNA)以及多嘧啶序列结合蛋白(PTB;不均一核糖核蛋白I)(Ghetti,A.,S. PinolRoma,W.M. Michael,C. Morandi,和G. Dreyfuss. 1992. 《核酸研究》20:3671 - 3678;Matera,A.G.,M.R. Frey,K. Margelot,和S.L. Wolin. 1995. 《细胞生物学杂志》129:1181 - 1193;Lee,B.,A.G. Matera,D.C. Ward,和J. Craft. 1996. 《美国国家科学院院刊》93: 11471 - 11476)。在本报告中,我们在固定细胞和活细胞中进一步对该结构进行了表征。在大量人类癌细胞和正常细胞中检测核仁周边区表明,核仁周边区在癌细胞中更为普遍。通过使用特异性识别PTB的单克隆抗体SH54进行免疫标记,对细胞周期进行分析,结果表明核仁周边区在有丝分裂开始时解离,并在末期后期在子核中重新形成。为了在活细胞中可视化核仁周边区,构建了PTB与绿色荧光蛋白(GFP)的融合蛋白。延时研究表明,核仁周边区的大小和形状随时间动态变化。此外,对最佳固定细胞进行电子显微镜检查发现,核仁周边区由多条链组成,每条链的直径约为80 - 180 nm。一些链与核仁表面直接接触。此外,使用GFP - PTB融合蛋白的一系列缺失突变体分析将PTB靶向核仁周边区的序列要求,结果表明融合蛋白靶向核仁周边区至少需要COOH或NH2末端的三个RNA识别基序(RRMs)。这一发现表明,RNA结合可能是PTB定位于核仁周边区所必需的。