Mesika Adi, Kiss Vladimir, Brumfeld Vlad, Ghosh Gourisankar, Reich Ziv
Department of Biological Chemistry, Weizmann Institute of Science, Rehovot 76100, Israel.
Hum Gene Ther. 2005 Feb;16(2):200-8. doi: 10.1089/hum.2005.16.200.
The use of synthetic gene delivery systems in human gene transfer is hampered by poor transfection efficiencies, largely because of the inability of DNA to translocate across the nuclear pore complex. A means to overcome this barrier is to bind the DNA to nuclear localization signals (NLSs), which are recognized by shuttling receptors of the nuclear import machinery. Here, we studied the intracellular transport of plasmid DNA microinjected into HeLa cell cytoplasm, alone or as a complex with intact or NLS-deleted NFkappaB p50, using confocal microscopy imaging. We found that association of NLS-carrying p50 with DNA facilitated not only nuclear entry of the DNA but also its migration through the cytoplasm toward the nucleus. Facilitated transport of p50-DNA complexes in the cytoplasm proceeded along microtubules in a dynein-dependent manner and is mediated by the heterodimeric nuclear transport receptor that recognizes the p50-born NLS.
合成基因递送系统在人类基因转移中的应用受到转染效率低下的阻碍,这主要是因为DNA无法穿过核孔复合体。克服这一障碍的一种方法是将DNA与核定位信号(NLSs)结合,核定位信号可被核输入机制的穿梭受体识别。在这里,我们使用共聚焦显微镜成像研究了微注射到HeLa细胞质中的质粒DNA的细胞内运输,该质粒DNA单独存在或与完整的或缺失NLS的NFκB p50形成复合物。我们发现携带NLS的p50与DNA的结合不仅促进了DNA进入细胞核,还促进了其在细胞质中向细胞核的迁移。p50-DNA复合物在细胞质中的易化运输以动力蛋白依赖的方式沿着微管进行,并由识别p50携带的NLS的异二聚体核运输受体介导。