首页> 外文期刊>Nucleic Acids Research >Nrf1 in a complex with fosB, c-jun, junD and ATF2 forms the AP1 component at the TNF alpha promoter in stimulated mast cells.
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Nrf1 in a complex with fosB, c-jun, junD and ATF2 forms the AP1 component at the TNF alpha promoter in stimulated mast cells.

机译:与fosB,c-jun,junD和ATF2形成复合体的Nrf1在受刺激的肥大细胞中的TNFα启动子处形成AP1组分。

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摘要

Cap 'n' collar-basic leucine zipper (CNC-bZIP) proteins are widely implicated in developmental processes throughout different species. Evidence is accumulating that some of them are also participating in induced gene expression in the adult. Here we show that the three CNC-bZIP members NF-E2, Nrf1 and Nrf2 are constitutively expressed in the murine mast cell line CPII and that they form transcription factor complexes with several AP1 binding proteins. Upon induction, complexes are observed at the 2 x NF-E2 consensus binding site and the extended kappa3/AP1(+) site of the TNFalpha promoter. The interaction of Nrf1 with c -jun, junD, fosB and ATF2 in mast cells is in contrast to the recently reported binding of Nrf1 alone at the kappa3/AP1(-) site in dendritic cells. We speculated that this may be the result of the expression of isoforms of Nrf1 in mast cells. Using a PCR cloning strategy, we have isolated six novel splice variants of this transcription factor. Some of them have deleted the translational stop codon, resulting in an Nrf1 protein with an altered leucine zipper region. Expression of this altered binding/interaction domain interferes with TNFalpha induction, indicating an interaction of this splice variant with the active AP1/NF-AT complex at this promoter.
机译:Cap'n'衣领碱性亮氨酸拉链(CNC-bZIP)蛋白广泛涉及整个物种的发育过程。越来越多的证据表明,其中一些也参与了成年人的诱导基因表达。在这里,我们显示了三个CNC-bZIP成员NF-E2,Nrf1和Nrf2在鼠肥大细胞系CPII中组成性表达,它们与几种AP1结合蛋白形成转录因子复合物。诱导后,在2个NF-E2共有结合位点和TNFalpha启动子的扩展kappa3 / AP1(+)位点观察到复合物。 Nrf1与肥大细胞中c-jun,junD,fosB和ATF2的相互作用与树突状细胞中最近报道的Nrf1在kappa3 / AP1(-)位点的结合形成了对比。我们推测这可能是肥大细胞中Nrf1亚型表达的结果。使用PCR克隆策略,我们已经分离出该转录因子的六个新颖的剪接变体。其中一些已经删除了翻译终止密码子,导致Nrf1蛋白的亮氨酸拉链区域发生了变化。该改变的结合/相互作用域的表达干扰TNFα的诱导,表明该剪接变体与该启动子处的活性AP1 / NF-AT复合物的相互作用。

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