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IGH minisatellite suppression of USF-binding-site- and Eμ-mediated transcriptional activation of the adenovirus major late promoter

机译:IGH微卫星抑制腺病毒主要晚期启动子的USF结合位点和Eμ介导的转录激活

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摘要

The 50bp repeat unit of the minisatellite within the DH JH interval of the human immunoglobulin heavy chain locus binds a nuclear factor present in a wide variety of cell types. The binding site contains the myc/HLH motif, CACGTG, and represents a 15 of 17 base match for the USF/WLTF binding site adjacent to the adenovirus major late promoter (MLP). Unlike the USF/MLTF site, the IGH minisatellite possesses no enhancer activity. However, it can significantly suppress, in cis and in trans, USF-site-mediated transcriptional activation of the MLP. In murine myeloma cells, the IGH minisatellite can suppress, in trans, MLP activation by the murine heavy chain gene enhancer, Eμ. These activities potentially represent a DNA-based form of squelching.
机译:在人类免疫球蛋白重链基因座的D J H 区间内,小卫星的50bp重复单元与存在于多种细胞类型中的核因子结合。该结合位点包含myc / HLH基序CACGTG,并且代表与腺病毒主要晚期启动子(MLP)相邻的USF / WLTF结合位点的17个碱基匹配中的15个。与USF / MLTF站点不同,IGH小卫星不具有增强子活性。但是,它可以在顺式和反式中显着抑制USF位点介导的MLP转录激活。在鼠骨髓瘤细胞中, IGH 小卫星可以反过来抑制鼠重链基因增强子Eμ激活MLP。这些活动可能代表了基于DNA的静噪形式。

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