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小鼠白细胞介素4基因的最佳转录需要四个P样元件:一组不同的活化T细胞核因子和激活蛋白-1家族蛋白的参与。

Four P-like elements are required for optimal transcription of the mouse IL-4 gene: involvement of a distinct set of nuclear factor of activated T cells and activator protein-1 family proteins.

作者信息

Takemoto N, Koyano-Nakagawa N, Arai N, Arai K, Yokota T

机构信息

Department of Stem Cell Regulation, Institute of Medical Science, University of Tokyo, Japan.

出版信息

Int Immunol. 1997 Sep;9(9):1329-38. doi: 10.1093/intimm/9.9.1329.

Abstract

We previously identified the P sequence as a critical regulatory element of the human IL-4 promoter. In the mouse IL-4 promoter, there are five elements homologous to the human P sequence designated conserved lymphokine element 0 (CLE0), P, P2, P3 and P4. To characterize the role of these P-like elements and their binding factors in the native promoter, we did transient transfection and electrophoretic mobility shift assays (EMSA). Transfection of EL-4 cells with the IL-4 promoter-reporter constructs carrying mutated P-like elements showed that four P-like elements, CLE0, P, P2 and P4, but not P3, were required for optimal activation of the IL-4 promoter. EMSA showed that both constitutive and inducible complexes bound to CLE0, P, P2 and P4, whereas only a constitutive complex bound to P3. In competition and antibody supershift assays in EMSA, complexes formed with P or P2 proved to contain nuclear factor of activated T cells (NFAT) family proteins as major components. Activator protein (AP)-1 family proteins interacted with CLE0, P, P2 and P4. NFAT/AP-1 complex formed only with P and P2. Cross-competition assays among the P-like elements revealed element-specific and common complexes. Six tandem repeats of the P element linked to the SV40 promoter responded to phorbol 12-myristate 13-acetate, while that of other elements did not. It would thus appear that components of each P-like element-binding complexes are not identical and may coordinately contribute to transcriptional activity.

摘要

我们之前将P序列鉴定为人白细胞介素-4(IL-4)启动子的关键调控元件。在小鼠IL-4启动子中,有五个与人类P序列同源的元件,分别命名为保守淋巴因子元件0(CLE0)、P、P2、P3和P4。为了表征这些类P元件及其结合因子在天然启动子中的作用,我们进行了瞬时转染和电泳迁移率变动分析(EMSA)。用携带突变类P元件的IL-4启动子-报告基因构建体转染EL-4细胞,结果表明,四个类P元件,即CLE0、P、P2和P4,而非P3,是IL-4启动子最佳激活所必需的。EMSA显示,组成型和诱导型复合物均与CLE0、P、P2和P4结合,而只有组成型复合物与P3结合。在EMSA的竞争和抗体超迁移分析中,与P或P2形成的复合物被证明主要包含活化T细胞核因子(NFAT)家族蛋白。激活蛋白(AP)-1家族蛋白与CLE0、P、P2和P4相互作用。NFAT/AP-1复合物仅与P和P2形成。类P元件之间的交叉竞争分析揭示了元件特异性和共同的复合物。与SV40启动子相连的P元件的六个串联重复序列对佛波醇12-肉豆蔻酸酯13-乙酸酯有反应,而其他元件的则没有。因此,每个类P元件结合复合物的成分似乎并不相同,可能协同促进转录活性。

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