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核因子κB2是活化的Notch-1通过重组信号结合蛋白Jκ(RBP-Jκ)的一个假定靶基因。

NF-kappaB2 is a putative target gene of activated Notch-1 via RBP-Jkappa.

作者信息

Oswald F, Liptay S, Adler G, Schmid R M

机构信息

Department of Internal Medicine, University of Ulm, Germany.

出版信息

Mol Cell Biol. 1998 Apr;18(4):2077-88. doi: 10.1128/MCB.18.4.2077.

Abstract

NF-kappaB2 (p100/p52), a member of the NF-kappaB/Rel family of transcription factors, is involved in the regulation of a variety of genes important for immune function. Previously, we have shown that the NF-kappaB2 gene is regulated in a positive and a negative manner. Two kappaB elements within the NF-kappaB2 promoter mediate tumor necrosis factor alpha-inducible transactivation. In addition, we have shown that there exists a transcriptional repression in the absence of NF-kappaB. To identify a DNA binding activity responsible for this transcriptional repression, we have partially purified a nuclear complex, named Rep-kappaB. Here we further analyze this putative repressive binding activity. Detailed examination of Rep-kappaB-DNA interaction revealed the sequence requirements for binding to be almost identical to those of recombination signal binding protein Jkappa (RBP-Jkappa), the mammalian homolog of the protein encoded by Drosophila suppressor of hairless [Su(H)]. In addition, in electromobility shift assays, Rep-kappaB binding activity is recognized by an antibody directed against RBP-Jkappa. By performing transient-transfection assays, we show that human RBP-Jkappa represses basal as well as RelA (p65)-stimulated NF-kappaB2 promoter activity. Studies in Drosophila melanogaster have shown that Su(H) is implicated in the Notch signaling pathway regulating cell fate decisions. In transient-transfection assays we show that truncated Notch-1 strongly induces NF-kappaB2 promoter activity. In summary, our data clearly demonstrate that Rep-kappaB is closely related or identical to RBP-Jkappa. RBP-Jkappa is a strong transcriptional repressor of NF-kappaB2. Moreover, this repression can be overcome by activated Notch-1, suggesting that NF-kappaB2 is a novel putative Notch target gene.

摘要

核因子-κB2(p100/p52)是核因子-κB/Rel转录因子家族的成员之一,参与调控多种对免疫功能至关重要的基因。此前,我们已经表明核因子-κB2基因受到正向和负向调控。核因子-κB2启动子内的两个κB元件介导肿瘤坏死因子α诱导的反式激活。此外,我们还表明在缺乏核因子-κB的情况下存在转录抑制。为了鉴定负责这种转录抑制的DNA结合活性,我们部分纯化了一种名为Rep-κB的核复合物。在此我们进一步分析这种假定的抑制性结合活性。对Rep-κB与DNA相互作用的详细研究揭示,其结合的序列要求与重组信号结合蛋白Jκ(RBP-Jκ)几乎相同,RBP-Jκ是果蝇无翅抑制因子[Su(H)]编码蛋白的哺乳动物同源物。此外,在电泳迁移率变动分析中,Rep-κB结合活性可被针对RBP-Jκ的抗体识别。通过进行瞬时转染分析,我们发现人RBP-Jκ可抑制基础以及RelA(p65)刺激的核因子-κB2启动子活性。对黑腹果蝇的研究表明,Su(H)参与Notch信号通路调控细胞命运决定。在瞬时转染分析中我们发现,截短的Notch-1强烈诱导核因子-κB2启动子活性。总之,我们的数据清楚地表明Rep-κB与RBP-Jκ密切相关或相同。RBP-Jκ是核因子-κB2的强转录抑制因子。此外,这种抑制可被激活的Notch-1克服,这表明核因子-κB2是一个新的假定的Notch靶基因。

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