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白细胞介素-4、白细胞介素-13和γ干扰素通过共享的DNA结合基序激活基因转录。

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

作者信息

Köhler I, Alliger P, Rieber E P

机构信息

Institute for Immunology, Ludwig-Maximilians-University, München, Germany.

出版信息

Behring Inst Mitt. 1995 Jun(96):78-86.

PMID:7575355
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.

摘要

白细胞介素-4(IL-4)和白细胞介素-13(IL-13)均可诱导转录因子NF-IL4(核因子IL-4),该因子以无活性形式预先存在,并与IL-4/IL-13依赖性基因启动子区域中的IL-4反应元件(IL-4RE)结合。紫外线交联和SDS凝胶电泳表明,NF-IL4至少由两个50 kDa和100 - 130 kDa的DNA结合成分组成。IL-4反应元件也被一种干扰素-γ(IFN-γ)诱导的DNA结合蛋白识别,该蛋白的分子量已确定为50 kDa。不同转录因子的共同DNA结合基序可能为IL-4/IL-13与IFN-γ之间频繁观察到的功能拮抗提供基础。IL-4/IL-13和IFN-γ对转录因子的激活可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,这表明这些细胞因子具有相关的信号转导途径。

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