Calomme Claire, Nguyen Thi Lien-Anh, de Launoit Yvan, Kiermer Veronique, Droogmans Louis, Burny Arsene, Van Lint Carine
Université Libre de Bruxelles, Institut de Biologie et de Médecine Moléculaires, Service de Chimie Biologique, Laboratoire de Virologie Moléculaire, Rue des Profs Jeener et Brachet 12, 6041 Gosselies, Belgium.
J Biol Chem. 2002 Mar 15;277(11):8775-89. doi: 10.1074/jbc.M107441200. Epub 2001 Dec 10.
The bovine leukemia virus (BLV) promoter is located in its 5'-long terminal repeat and is composed of the U3, R, and U5 regions. BLV transcription is regulated by cis-acting elements located in the U3 region, including three 21-bp enhancers required for transactivation of the BLV promoter by the virus-encoded transactivator Tax(BLV). In addition to the U3 cis-acting elements, both the R and U5 regions contain stimulatory sequences. To date, no transcription factor-binding site has been identified in the R region. Here sequence analysis of this region revealed the presence of a potential E box motif (5'-CACGTG-3'). By competition and supershift gel shift assays, we demonstrated that the basic helix-loop-helix transcription factors USF1 and USF2 specifically interacted with this R region E box motif. Mutations abolishing upstream stimulatory factor (USF) binding caused a reproducible decrease in basal or Tax-activated BLV promoter-driven gene expression in transient transfection assays of B-lymphoid cell lines. Cotransfection experiments showed that the USF1 and USF2a transactivators were able to act through the BLV R region E box. Taken together, these results physically and functionally characterize a USF-binding site in the R region of BLV. This E box motif located downstream of the transcription start site constitutes a new positive regulatory element involved in the transcriptional activity of the BLV promoter and could play an important role in virus replication.
牛白血病病毒(BLV)启动子位于其5'-长末端重复序列中,由U3、R和U5区域组成。BLV转录受位于U3区域的顺式作用元件调控,包括病毒编码的反式激活因子Tax(BLV)反式激活BLV启动子所需的三个21bp增强子。除U3顺式作用元件外,R和U5区域均含有刺激序列。迄今为止,尚未在R区域鉴定出转录因子结合位点。在此,对该区域的序列分析揭示了一个潜在的E盒基序(5'-CACGTG-3')。通过竞争和超迁移凝胶迁移试验,我们证明碱性螺旋-环-螺旋转录因子USF1和USF2与该R区域E盒基序特异性相互作用。在B淋巴细胞系的瞬时转染试验中,消除上游刺激因子(USF)结合的突变导致基础或Tax激活的BLV启动子驱动的基因表达可重复性降低。共转染实验表明,USF1和USF2a反式激活因子能够通过BLV R区域E盒发挥作用。综上所述,这些结果从物理和功能上对BLV R区域中的一个USF结合位点进行了表征。这个位于转录起始位点下游的E盒基序构成了一个参与BLV启动子转录活性的新的正调控元件,可能在病毒复制中发挥重要作用。