Huang S, Deerinck T J, Ellisman M H, Spector D L
Department of Cell and Molecular Biology, Northwestern University Medical School, Chicago, Illinois 60611, USA.
J Cell Biol. 1998 Oct 5;143(1):35-47. doi: 10.1083/jcb.143.1.35.
The perinucleolar compartment (PNC) is a unique nuclear structure localized at the periphery of the nucleolus. Several small RNAs transcribed by RNA polymerase III and two hnRNP proteins have been localized in the PNC (Ghetti, A., S. Piñol-Roma, 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; Timchenko, L.T., J.W. Miller, N.A. Timchenko, D.R. DeVore, K.V. Datar, L. Lin, R. Roberts, C.T. Caskey, and M.S. Swanson. 1996. Nucleic Acids Res. 24: 4407-4414; Huang, S., T. Deerinck, M.H. Ellisman, and D.L. Spector. 1997. J. Cell Biol. 137:965-974). In this report, we show that the PNC incorporates Br-UTP and FITC-conjugated CTP within 5 min of pulse labeling. Selective inhibition of RNA polymerase I does not appreciably affect the nucleotide incorporation in the PNC. Inhibition of all RNA polymerases by actinomycin D blocks the incorporation completely, suggesting that Br-UTP incorporation in the PNC is due to transcription by RNA polymerases II and/or III. Treatment of cells with an RNA polymerase II and III inhibitor induces a significant reorganization of the PNC. In addition, double labeling experiments showed that poly(A) RNA and some of the factors required for pre-mRNA processing were localized in the PNC in addition to being distributed in their previously characterized nucleoplasmic domains. Fluorescence recovery after photobleaching (FRAP) analysis revealed a rapid turnover of polypyrimidine tract binding protein within the PNC, demonstrating the dynamic nature of the structure. Together, these findings suggest that the PNC is a functional compartment involved in RNA metabolism in the cell nucleus.
核仁周边区(PNC)是一种位于核仁周边的独特核结构。由RNA聚合酶III转录的几种小RNA以及两种异质性核糖核蛋白(hnRNP)已定位在PNC中(Ghetti, A., S. Piñol-Roma, W.M. Michael, C. Morandi, and G. Dreyfuss. 1992. 《核酸研究》20:3671 - 3678;Matera, A.G., M.R. Frey, K. Margelot, and S.L. Wolin. 1995. 《细胞生物学杂志》129:1181 - 1193;Timchenko, L.T., J.W. Miller, N.A. Timchenko, D.R. DeVore, K.V. Datar, L. Lin, R. Roberts, C.T. Caskey, and M.S. Swanson. 1996. 《核酸研究》24: 4407 - 4414;Huang, S., T. Deerinck, M.H. Ellisman, and D.L. Spector. 1997. 《细胞生物学杂志》137:965 - 974)。在本报告中,我们表明PNC在脉冲标记5分钟内就会掺入溴尿苷三磷酸(Br - UTP)和异硫氰酸荧光素(FITC)偶联的胞苷三磷酸(CTP)。对RNA聚合酶I的选择性抑制对PNC中的核苷酸掺入没有明显影响。放线菌素D对所有RNA聚合酶的抑制会完全阻断掺入,这表明PNC中Br - UTP的掺入是由于RNA聚合酶II和/或III的转录。用RNA聚合酶II和III抑制剂处理细胞会导致PNC发生显著的重新组织。此外,双重标记实验表明,聚腺苷酸(poly(A))RNA和一些前体mRNA加工所需的因子除了分布在其先前已确定的核质区域外,也定位在PNC中。光漂白后荧光恢复(FRAP)分析显示PNC内的多嘧啶序列结合蛋白有快速周转,证明了该结构的动态性质。总之,这些发现表明PNC是细胞核中参与RNA代谢的一个功能区室。