Lee S, Neumann M, Stearman R, Stauber R, Pause A, Pavlakis G N, Klausner R D
Cell Biology and Metabolism Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, USA.
Mol Cell Biol. 1999 Feb;19(2):1486-97. doi: 10.1128/MCB.19.2.1486.
Mutation of the von Hippel-Lindau tumor suppressor gene (vhl) causes the von Hippel-Lindau cancer syndrome as well as sporadic renal clear cell carcinoma. To pursue our study of the intracellular localization of VHL protein in relation to its function, we fused VHL to the green fluorescent protein (GFP) to produce the VHL-GFP fusion protein. Like VHL, VHL-GFP binds to elongins B and C and Cullin-2 and regulates target gene product levels, including levels of vascular endothelial growth factor and glucose transporter 1. VHL-GFP localizes predominantly to the cytoplasm, with some detectable nuclear signal. Inhibition of transcription by actinomycin D or 5,6-dichlorobenzimidazole riboside (DRB) causes VHL to be redistributed to the nucleus. A cellular fusion assay was used to demonstrate that inhibition of transcription induces a decrease in the nuclear export rate of VHL. The dependence of transcription for trafficking is lost with a deletion of exon 2, a region with a mutation causing a splice defect in the VHL gene in sporadic renal clear cell carcinoma. Addition of a strong nuclear export signal (NES) derived from the Rev protein results in complete nuclear exclusion and abrogates the redistribution of VHL-GFP-NES into the nucleus upon inhibition of transcription. Leptomycin B, which inhibits NES-mediated nuclear export, reverts the distribution of VHL-GFP-NES to that of VHL-GFP and restores sensitivity to actinomycin D and DRB. Uncoupling of VHL-GFP trafficking to transcription either by an exon 2 deletion or fusion to NES abolishes VHL function. We suggest that VHL function requires not only nuclear or cytoplasmic localization, but also exon 2-mediated transcription-dependent trafficking between these two cellular compartments.
冯·希佩尔-林道肿瘤抑制基因(vhl)的突变会导致冯·希佩尔-林道癌症综合征以及散发性肾透明细胞癌。为了开展关于VHL蛋白细胞内定位与其功能关系的研究,我们将VHL与绿色荧光蛋白(GFP)融合,以产生VHL-GFP融合蛋白。与VHL一样,VHL-GFP与延伸蛋白B和C以及Cullin-2结合,并调节靶基因产物水平,包括血管内皮生长因子和葡萄糖转运蛋白1的水平。VHL-GFP主要定位于细胞质,有一些可检测到的核信号。放线菌素D或5,6-二氯苯并咪唑核糖核苷(DRB)抑制转录会导致VHL重新分布到细胞核。细胞融合试验用于证明转录抑制会导致VHL的核输出率降低。外显子2缺失后,转录对转运的依赖性丧失,外显子2区域的突变会导致散发性肾透明细胞癌中VHL基因出现剪接缺陷。添加源自Rev蛋白的强核输出信号(NES)会导致完全核排斥,并消除转录抑制时VHL-GFP-NES向细胞核的重新分布。抑制NES介导的核输出的雷帕霉素B会使VHL-GFP-NES的分布恢复为VHL-GFP的分布,并恢复对放线菌素D和DRB的敏感性。通过外显子2缺失或与NES融合使VHL-GFP转运与转录解偶联会消除VHL功能。我们认为,VHL功能不仅需要核定位或细胞质定位,还需要外显子2介导的这两个细胞区室之间的转录依赖性转运。