Tripathi Kaushlendra, Parnaik Veena K
Centre for Cellular and Molecular Biology, Hyderabad, India.
J Biosci. 2008 Sep;33(3):345-54. doi: 10.1007/s12038-008-0054-3.
Pre-mRNA splicing factors are enriched in nuclear domains termed interchromatin granule clusters or nuclear speckles. During mitosis, nuclear speckles are disassembled by metaphase and reassembled in telophase in structures termed mitotic interchromatin granules (MIGs). We analysed the dynamics of the splicing factor SC35 in interphase and mitotic cells. In HeLa cells expressing green fluorescent protein (GFP)-SC35, this was localized in speckles during interphase and dispersed in metaphase. In telophase, GFP-SC35 was highly enriched within telophase nuclei and also detected in MIGs. Fluorescence recovery after photobleaching (FRAP) experiments revealed that the mobility of GFP-SC35 was distinct in different mitotic compartments. Interestingly, the mobility of GFP-SC35 was 3-fold higher in the cytoplasm of metaphase cells compared with interphase speckles, the nucleoplasm or MIGs. Treatment of cells with inhibitors of cyclin-dependent kinases (cdks) caused changes in the organization of nuclear compartments such as nuclear speckles and nucleoli, with corresponding changes in the mobility of GFP-SC35 and GFP-fibrillarin. Our results suggest that the dynamics of SC35 are significantly influenced by the organization of the compartment in which it is localized during the cell cycle.
前体mRNA剪接因子在称为染色质间颗粒簇或核斑点的核结构域中富集。在有丝分裂期间,核斑点在中期解体,并在末期重新组装成称为有丝分裂染色质间颗粒(MIG)的结构。我们分析了剪接因子SC35在间期和有丝分裂细胞中的动态变化。在表达绿色荧光蛋白(GFP)-SC35的HeLa细胞中,其在间期定位于斑点中,并在中期分散。在末期,GFP-SC35在末期细胞核中高度富集,并且在MIG中也能检测到。光漂白后荧光恢复(FRAP)实验表明,GFP-SC35在不同的有丝分裂区室中的流动性不同。有趣的是,与间期斑点、核质或MIG相比,GFP-SC35在中期细胞细胞质中的流动性高3倍。用细胞周期蛋白依赖性激酶(cdk)抑制剂处理细胞会导致核区室如核斑点和核仁的组织发生变化,同时GFP-SC35和GFP-原纤维蛋白的流动性也会相应改变。我们的结果表明,SC35的动态变化受到其在细胞周期中所处区室组织的显著影响。