Zanta M A, Belguise-Valladier P, Behr J P
Laboratoire de Chimie Génétique associé Centre National de la Recherche Scientifique/Université Louis Pasteur (Unité Mixte de Recherche 7514), Faculté de Pharmacie de Strasbourg, France.
Proc Natl Acad Sci U S A. 1999 Jan 5;96(1):91-6. doi: 10.1073/pnas.96.1.91.
Translocation of exogenous DNA through the nuclear membrane is a major concern of gene delivery technologies. To take advantage of the cellular import machinery, we have synthesized a capped 3.3-kbp CMVLuciferase-NLS gene containing a single nuclear localization signal peptide (PKKKRKVEDPYC). Transfection of cells with the tagged gene remained effective down to nanogram amounts of DNA. Transfection enhancement (10- to 1,000-fold) as a result of the signal peptide was observed irrespective of the cationic vector or the cell type used. A lysine to threonine mutation of the third NLS amino acid completely abolished these remarkable features, suggesting importin-mediated translocation. Our hypothesis is that the 3-nm-wide DNA present in the cytoplasm is initially docked to and translocated through a nuclear pore by the nuclear import machinery. As DNA enters the nucleus, it is quickly condensed into a chromatin-like structure, which provides a mechanism for threading the remaining worm-like molecule through the pore. A single NLS signal is thus sufficient, whereas many signals on a gene would actually inhibit entry, the same DNA molecule being threaded through adjacent pores.
外源DNA穿过核膜的转运是基因递送技术的一个主要关注点。为了利用细胞的导入机制,我们合成了一个带帽的3.3千碱基对的CMV荧光素酶-NLS基因,其包含一个单核定位信号肽(PKKKRKVEDPYC)。用标记基因转染细胞时,即使DNA用量低至纳克量仍保持有效。无论使用阳离子载体或细胞类型如何,均观察到信号肽导致的转染增强(10至1000倍)。核定位信号第三个氨基酸的赖氨酸到苏氨酸突变完全消除了这些显著特征,提示为输入蛋白介导的转运。我们的假设是,存在于细胞质中的3纳米宽的DNA最初与核输入机制对接并通过核孔转运。随着DNA进入细胞核,它迅速浓缩成类似染色质的结构,这为将剩余的蠕虫状分子穿过核孔提供了一种机制。因此单个核定位信号就足够了,而基因上的多个信号实际上会抑制进入,同一DNA分子通过相邻核孔穿行。