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在一种小鼠巨噬细胞系中,γ干扰素和肿瘤坏死因子α对II类基因调控所需的顺式作用序列。

cis-acting sequences required for class II gene regulation by interferon gamma and tumor necrosis factor alpha in a murine macrophage cell line.

作者信息

Freund Y R, Dedrick R L, Jones P P

机构信息

Department of Immunology and Infectious Diseases, Palo Alto Medical Foundation, California 94301.

出版信息

J Exp Med. 1990 Apr 1;171(4):1283-99. doi: 10.1084/jem.171.4.1283.

Abstract

In this report, we have demonstrated that IFN-gamma and TNF-alpha increase expression of both the I-A and I-E region gene products on the surface of the myelomonocytic cell line WEHI-3, and that they mediate this increase via an increase in A alpha transcription. Constructs containing 5' deletion mutations of the A alpha promoter attached to the bacterial chloramphenicol acetyl transferase gene were used to delineate the minimum 5' flanking sequences required for promoter activity, and for inducibility by IFN-gamma and TNF-alpha. Approximately 115 bp of 5' sequences are required for minimum induction by IFN-gamma or TNF-alpha when the cytokines are present separately. This includes the three conserved promoter elements, the X, Y, and H boxes. Nested linker-scanner mutations demonstrated that additional regions were also critical for optimal induction by IFN-gamma or TNF-alpha. These include the kappa B-like enhancer and a TNF-alpha-specific sequence that we have tentatively called the T box. The T box sequence was also found in the promoter regions of the human HLA-DQ alpha and rat RT1.B alpha genes. Although the entire T box sequence element was not found in the other mouse class II genes, all class II alpha genes contained the SV40 core enhancer element in the regions included by the T box. Mouse class II beta genes appear to contain neither the T box nor the core enhancer element in this region, suggesting differential regulation of class II alpha and beta genes by TNF-alpha.

摘要

在本报告中,我们已证明,γ干扰素(IFN-γ)和肿瘤坏死因子-α(TNF-α)可增加骨髓单核细胞系WEHI-3表面I-A和I-E区基因产物的表达,且它们通过增加Aα转录来介导这种增加。含有与细菌氯霉素乙酰转移酶基因相连的Aα启动子5'缺失突变的构建体被用于确定启动子活性以及IFN-γ和TNF-α诱导所需的最小5'侧翼序列。当细胞因子单独存在时,IFN-γ或TNF-α的最小诱导需要约115 bp的5'序列。这包括三个保守的启动子元件,即X、Y和H盒。嵌套的接头扫描突变表明,其他区域对于IFN-γ或TNF-α的最佳诱导也至关重要。这些区域包括κB样增强子和一个我们暂称为T盒的TNF-α特异性序列。在人HLA-DQα和大鼠RT1.Bα基因的启动子区域中也发现了T盒序列。虽然在其他小鼠II类基因中未发现完整的T盒序列元件,但所有II类α基因在T盒所包含的区域中都含有SV40核心增强子元件。小鼠II类β基因在该区域似乎既不含有T盒也不含有核心增强子元件,这表明TNF-α对II类α和β基因的调控存在差异。

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