Quensel Christina, Friedrich Beate, Sommer Thomas, Hartmann Enno, Kohler Matthias
Osteeklinik Damp GmbH, Sente-Deern-Ring 30, 24351 Osteebad Damp, Germany.
Mol Cell Biol. 2004 Dec;24(23):10246-55. doi: 10.1128/MCB.24.23.10246-10255.2004.
The "classical" nuclear import pathway depends on importins alpha and beta. Humans have only one importin beta, while six alpha importins have been described. Whether or not distinct alpha importins are essential for specific import pathways in living human cells is unclear. We used RNA interference technology to specifically down-regulate the expression of ubiquitously expressed human alpha importins in HeLa cells. Down-regulation of importins alpha3, alpha5, alpha7, and beta strongly inhibited HeLa cell proliferation, while down-regulation of importins alpha1 and alpha4 had only a minor effect or no effect. Nucleoplasmin import was not prevented by down-regulation of any alpha importin, indicating that the importin alpha/beta pathway was generally not affected. In contrast, importin alpha3 or alpha5 down-regulation specifically inhibited the nuclear import of the Ran guanine nucleotide exchange factor, RCC1. Coinjection of recombinant alpha importins and RCC1 into down-regulated cells demonstrated that these transport defects were specifically caused by the limited availability of importin alpha3 in both cases. Thus, importin alpha3 is the only alpha importin responsible for the classical nuclear import of RCC1 in living cells.
“经典”核输入途径依赖于输入蛋白α和β。人类只有一种输入蛋白β,而已描述的输入蛋白α有六种。在活的人类细胞中,不同的输入蛋白α对于特定的输入途径是否必不可少尚不清楚。我们使用RNA干扰技术在HeLa细胞中特异性下调普遍表达的人类输入蛋白α的表达。下调输入蛋白α3、α5、α7和β强烈抑制HeLa细胞增殖,而下调输入蛋白α1和α4只有轻微影响或没有影响。核质蛋白的输入不会因任何输入蛋白α的下调而受到阻碍,这表明输入蛋白α/β途径通常不受影响。相比之下,下调输入蛋白α3或α5会特异性抑制Ran鸟嘌呤核苷酸交换因子RCC1的核输入。将重组输入蛋白α和RCC1共注射到下调的细胞中表明,在这两种情况下,这些转运缺陷都是由输入蛋白α3的可用性有限特异性导致的。因此,输入蛋白α3是活细胞中负责RCC1经典核输入的唯一输入蛋白α。