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Differential Dynamics Of Splicing Factor Sc35 During The Cell Cycle

机译:剪接因子Sc35在细胞周期中的差异动力学

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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.
机译:mRNA前剪接因子富集在称为染色质间颗粒簇或核斑点的核域中。在有丝分裂期间,核斑点通过中期分裂,并在末期重新组装在称为有丝分裂染色质间颗粒(MIG)的结构中。我们分析了剪接因子SC35在相间和有丝分裂细胞中的动力学。在表达绿色荧光蛋白(GFP)-SC35的HeLa细胞中,其在相间定位于斑点,并在中期分散。在末期,GFP-SC35在末期细胞核内高度富集,并在MIG中检测到。光漂白(FRAP)实验后的荧光恢复表明,GFP-SC35的迁移率在不同的有丝分裂区室中是不同的。有趣的是,与相间斑点,核质或MIG相比,GFP-SC35在中期细胞的细胞质中的迁移率高3倍。用细胞周期蛋白依赖性激酶(cdks)抑制剂处理细胞会导致核区室(如核斑和核仁)的组织变化,以及GFP-SC35和GFP-纤蛋白的迁移率发生相应变化。我们的研究结果表明,SC35的动力学受到细胞周期中局部区域的组织的显着影响。

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