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小鼠白细胞介素-5基因启动子顺式调控元件的定义。活化T细胞核因子相关因子参与白细胞介素-5的表达。

Definition of cis-regulatory elements of the mouse interleukin-5 gene promoter. Involvement of nuclear factor of activated T cell-related factors in interleukin-5 expression.

作者信息

Lee H J, Masuda E S, Arai N, Arai K, Yokota T

机构信息

Department of Molecular and Developmental Biology, University of Tokyo, Japan.

出版信息

J Biol Chem. 1995 Jul 21;270(29):17541-50. doi: 10.1074/jbc.270.29.17541.

DOI:10.1074/jbc.270.29.17541
PMID:7615560
Abstract

We have previously reported that the promoter region of the mouse interleukin-5 (IL-5) gene, extending from a nucleotide position about -1,200 to +33 relative to the transcription initiation site, can mediate transcriptional stimulation by phorbol 12-myristate 13-acetate and dibutyryl cAMP (Bt2cAMP) in mouse thymoma EL-4 cells. Here, we describe identification of four cis-regulatory elements necessary for full activity of the IL-5 promoter, using deletion and mutation analyses. We designated these elements as IL-5A (-948 approximately -933), IL-5P (-117 approximately -92), IL-5C (-74 approximately -56), and IL-5CLE0 (-55 approximately -38). We found that IL-5P bears homology to the binding site for the nuclear factor of activated T cells (NF-AT) and interacted with protein factors in nuclear extracts prepared from EL-4 cells stimulated with phorbol 12-myristate 13-acetate and Bt2cAMP (designated NFIL-5P). NFIL-5P complex was inhibited in the presence of an excess NF-AT and AP1 oligonucleotides and super-shifted by antisera raised against NF-ATp, c-Fos, and c-Jun. It thus seems likely that an NF-AT-related factor is involved in the regulation of IL-5 gene transcription.

摘要

我们先前曾报道,小鼠白细胞介素5(IL-5)基因的启动子区域,从相对于转录起始位点约-1200至+33的核苷酸位置延伸,可在小鼠胸腺瘤EL-4细胞中介导佛波醇12-肉豆蔻酸酯13-乙酸酯和二丁酰环磷腺苷(Bt2cAMP)的转录刺激。在此,我们通过缺失和突变分析描述了IL-5启动子完全活性所需的四个顺式调控元件的鉴定。我们将这些元件命名为IL-5A(-948至-933)、IL-5P(-117至-92)、IL-5C(-74至-56)和IL-5CLE0(-55至-38)。我们发现IL-5P与活化T细胞核因子(NF-AT)的结合位点具有同源性,并与用佛波醇12-肉豆蔻酸酯13-乙酸酯和Bt2cAMP刺激的EL-4细胞制备的核提取物中的蛋白质因子相互作用(命名为NFIL-5P)。在过量的NF-AT和AP1寡核苷酸存在下,NFIL-5P复合物受到抑制,并被针对NF-ATp、c-Fos和c-Jun产生的抗血清超迁移。因此,似乎一个与NF-AT相关的因子参与了IL-5基因转录的调控。

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