Yamaoka S, Courtois G, Bessia C, Whiteside S T, Weil R, Agou F, Kirk H E, Kay R J, Israël A
Unité de Biologie Moléculaire de l'Expression Génique, URA 1773 CNRS, Institut Pasteur, Paris, France.
Cell. 1998 Jun 26;93(7):1231-40. doi: 10.1016/s0092-8674(00)81466-x.
We have characterized a flat cellular variant of HTLV-1 Tax-transformed rat fibroblasts, 5R, which is unresponsive to all tested NF-kappaB activating stimuli, and we report here its genetic complementation. The recovered full-length cDNA encodes a 48 kDa protein, NEMO (NF-kappaB Essential MOdulator), which contains a putative leucine zipper motif. This protein is absent from 5R cells, is part of the high molecular weight IkappaB kinase complex, and is required for its formation. In vitro, NEMO can homodimerize and directly interacts with IKK-2. The NEMO cDNA was also able to complement another NF-kappaB-unresponsive cell line, 1.3E2, in which the protein is also absent, allowing us to demonstrate that this factor is required not only for Tax but also for LPS, PMA, and IL-1 stimulation of NF-kappaB activity.
我们已对人嗜T淋巴细胞病毒1型(HTLV-1)Tax转化的大鼠成纤维细胞的一种扁平细胞变体5R进行了特性分析,该变体对所有测试的NF-κB激活刺激均无反应,我们在此报告其基因互补情况。回收的全长cDNA编码一种48 kDa的蛋白质,即NEMO(NF-κB必需调节因子),它含有一个假定的亮氨酸拉链基序。该蛋白质在5R细胞中不存在,是高分子量IκB激酶复合物的一部分,并且是其形成所必需的。在体外,NEMO可以同二聚化并直接与IKK-2相互作用。NEMO cDNA还能够互补另一种NF-κB无反应性细胞系1.3E2,该细胞系中也不存在这种蛋白质,这使我们能够证明该因子不仅是Tax激活NF-κB活性所必需的,也是脂多糖(LPS)、佛波酯(PMA)和白细胞介素-1(IL-1)激活NF-κB活性所必需的。