Activation of gene transcription by IL-4, IL-13 and IFN-gamma through a shared DNA binding motif.

Behring Institute Mitteilungen Pub Date : 1995-06-01
I Köhler, P Alliger, E P Rieber
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引用次数: 0

Abstract

Both interleukin-4 (IL-4) and interleukin-13 (IL-13) induce the transcription factor NF-IL4 (nuclear factor IL-4) which preexists in an inactive form and binds to an IL-4 responsive element (IL-4RE) in the promoter regions of IL-4/IL-13-dependent genes. UV-crosslinking and SDS gel electrophoresis indicate that NF-IL4 consists of at least two DNA-binding components of 50 kDa and 100-130 kDa. The IL-4 responsive element is also recognized by an interferon-gamma (IFN-gamma)-induced DNA binding protein for which a Mr of 50 kDa has been determined. A common DNA binding motif for different transcription factors might provide the basis for the frequently observed functional antagonism between IL-4/IL-13 and IFN-gamma. The activation of transcription factors by IL-4/IL-13 and IFN-gamma could be blocked by inhibitors of tyrosine kinases and ser/thr phosphatases but not by a PKC inhibitor, suggesting related signal transduction pathways for these cytokines.

IL-4、IL-13和ifn - γ通过共享的DNA结合基序激活基因转录。
白细胞介素-4 (IL-4)和白细胞介素-13 (IL-13)都能诱导转录因子NF-IL4(核因子IL-4),该因子以非活性形式存在,并与IL-4/IL-13依赖基因的启动子区域中的IL-4应答元件(IL-4RE)结合。紫外交联和SDS凝胶电泳表明,NF-IL4至少包含50 kDa和100-130 kDa的两种dna结合成分。IL-4响应元件也被干扰素- γ (ifn - γ)诱导的DNA结合蛋白识别,其Mr已确定为50 kDa。不同转录因子的共同DNA结合基序可能为经常观察到的IL-4/IL-13与ifn - γ之间的功能拮抗提供了基础。IL-4/IL-13和ifn - γ对转录因子的激活可以被酪氨酸激酶和丝氨酸/苏氨酸磷酸酶抑制剂阻断,但不能被PKC抑制剂阻断,提示这些细胞因子有相关的信号转导途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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