Kanda K, Hu H M, Zhang L, Grandchamps J, Boxer L M
Center for Molecular Biology in Medicine, Veterans Affairs Palo Alto Health Care System and the Department of Medicine, Stanford University School of Medicine, Stanford, California 94305, USA.
J Biol Chem. 2000 Oct 13;275(41):32338-46. doi: 10.1074/jbc.M004148200.
The c-myc gene is translocated to one of the immunoglobulin genes in Burkitt's lymphoma resulting in deregulated expression of c-myc. Several enhancers have been shown to be important for expression of the immunoglobulin heavy chain gene. Four enhancer regions (murine-hypersensitive sites (MHS) 1, 2, 3, and 4) located 3' of the murine immunoglobulin heavy chain gene play a role in activating expression of the translocated c-myc gene. The enhancer regions also result in a shift in transcriptional initiation from the P2 promoter to P1 that is characteristic of the translocated c-myc allele. We found that the most 3' enhancer region (MHS4) activated the c-myc promoter by 46-fold in the Raji Burkitt's lymphoma cell line, and it was the most active enhancer in these cells. The addition of enhancer regions MHS1,2 and 3 to MHS4 increased c-myc transcription by an additional 3-fold and resulted in the full promoter shift from P2 to P1. By deletion analysis of enhancer region MHS4, we located a region that was critical for the transcriptional activity of MHS4. Electrophoretic mobility shift assay analysis revealed that NF-kappaB/Rel family members bound to this region. Mutation of the NF-kappaB binding site abolished both the enhancer activity and the promoter shift activity of MHS4. An active NF-kappaB site was also identified in the human HS4 enhancer. Inhibition of c-myc promoter activity driven by the immunoglobulin enhancers was observed with expression of a super-repressor IkappaBalpha construct. These results indicate that the NF-kappaB/Rel transcription factors play an important role in the deregulation of the translocated c-myc gene in Burkitt's lymphoma and suggest that interference with NF-kappaB function may represent a new approach to the treatment of Burkitt's lymphoma.
在伯基特淋巴瘤中,c-myc基因易位至免疫球蛋白基因之一,导致c-myc表达失调。已有研究表明,几种增强子对免疫球蛋白重链基因的表达很重要。位于小鼠免疫球蛋白重链基因3'端的四个增强子区域(小鼠超敏位点(MHS)1、2、3和4)在激活易位的c-myc基因表达中发挥作用。这些增强子区域还导致转录起始从P2启动子转变为P1,这是易位的c-myc等位基因的特征。我们发现,最3'端的增强子区域(MHS4)在Raji伯基特淋巴瘤细胞系中使c-myc启动子活性增强了46倍,并且它是这些细胞中最活跃的增强子。将增强子区域MHS1、2和3添加到MHS4中,可使c-myc转录额外增加3倍,并导致启动子完全从P2转变为P1。通过对增强子区域MHS4进行缺失分析,我们定位到了一个对MHS4转录活性至关重要的区域。电泳迁移率变动分析表明,NF-κB/Rel家族成员与该区域结合。NF-κB结合位点的突变消除了MHS4的增强子活性和启动子转变活性。在人HS4增强子中也鉴定出了一个活性NF-κB位点。用超抑制性IkappaBα构建体的表达可观察到免疫球蛋白增强子驱动的c-myc启动子活性受到抑制。这些结果表明,NF-κB/Rel转录因子在伯基特淋巴瘤中易位的c-myc基因失调中起重要作用,并提示干扰NF-κB功能可能代表一种治疗伯基特淋巴瘤的新方法。