Rothenberger S, Bachmann E, Berger C, McQuain C, Odermatt B F, Knecht H
Institut de Pharmacologie et Toxicologie, Université de Lausanne, Switzerland.
Oncogene. 1997 May 1;14(17):2123-6. doi: 10.1038/sj.onc.1201032.
An increasing number of reports shows a link between the Epstein-Barr virus (EBV) and lymphoid neoplasia. The latent membrane protein 1 (LMP1) is likely to play a determinant role in this process since this EBV encoded protein has oncogenic properties and is usually expressed in EBV-associated lymphoproliferative diseases (LPD), except Burkitt's lymphoma. We previously identified in LPD patients mutational hot spots and a 30 bp or 69 bp deletion in the LMP1 gene region coding for the C-terminal domain. These deletions are located in an area shown to be important for the activation of the transcription factor NF-kappaB. These findings lead us to test whether these natural deletion variants may have a functional effect. We measured the stimulation of their activity using a luciferase reporter plasmid containing NF-kappaB responsive elements. We tested the NF-kappaB inducing activity of four naturally occurring LMP1 deletion variants. Our results show that these deletion variants activate NF-kappaB to the same level as the wild-type form, indicating that the crucial residues for NF-kappaB activation are conserved among the variants isolated and lie within the last 32 amino acids of the C-terminal domain of the LMP1 oncogene.
越来越多的报告显示,爱泼斯坦-巴尔病毒(EBV)与淋巴样肿瘤之间存在联系。潜伏膜蛋白1(LMP1)可能在此过程中起决定性作用,因为这种EBV编码蛋白具有致癌特性,通常在EBV相关的淋巴增殖性疾病(LPD)中表达,但不包括伯基特淋巴瘤。我们之前在LPD患者中鉴定出了LMP1基因编码C末端结构域区域的突变热点以及30 bp或69 bp的缺失。这些缺失位于一个对转录因子NF-κB激活很重要的区域。这些发现促使我们测试这些天然缺失变体是否可能具有功能效应。我们使用含有NF-κB反应元件的荧光素酶报告质粒来测量它们活性的刺激情况。我们测试了四种天然存在的LMP1缺失变体诱导NF-κB的活性。我们的结果表明,这些缺失变体激活NF-κB的水平与野生型相同,这表明在分离出的变体中,NF-κB激活的关键残基是保守的,并且位于LMP1癌基因C末端结构域的最后32个氨基酸内。