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增强子A在核因子κB对经典和非经典HLA I类基因的位点特异性反式激活中的作用。

The role of enhancer A in the locus-specific transactivation of classical and nonclassical HLA class I genes by nuclear factor kappa B.

作者信息

Gobin S J, Keijsers V, van Zutphen M, van den Elsen P J

机构信息

Department of Immunohematology and Blood Bank, Leiden University Medical Center, The Netherlands.

出版信息

J Immunol. 1998 Sep 1;161(5):2276-83.

PMID:9725221
Abstract

HLA class I expression is tightly controlled at the transcriptional level by several conserved regulatory elements in the proximal promoter region. In this study, the two putative kappa B motifs of enhancer A (kappa B1 and kappa B2) of the classical and nonclassical HLA class I genes were investigated for their binding properties of transcription factors and tested for their contribution to the NF-kappa B-induced route of transactivation. It was shown that NF-kappa B-induced transactivation through enhancer A is most important for the HLA-A locus, which contains two NF-kappa B binding sites. Although the enhancer A of HLA-B contains only one NF-kappa B binding site (kappa B1), there was still a moderate transactivation by NF-kappa B. Since HLA-F, which also possesses one NF-kappa B binding site but lacks protein binding to its KB2 site, was not transactivated by NF-kappa B, the NF-kappa B-mediated transactivation through the kappa B1 motif in HLA-B is most probably facilitated by binding of the transcription factor Spl to the upstream kappa B2 site. Thus, transcriptional regulation of HLA class I genes by NF-kappa B is restricted to the HLA-A and HLA-B loci.

摘要

HLA I类分子的表达在转录水平上受到近端启动子区域中几个保守调控元件的严格控制。在本研究中,对经典和非经典HLA I类基因增强子A的两个假定κB基序(κB1和κB2)进行了转录因子结合特性研究,并测试了它们对NF-κB诱导的反式激活途径的贡献。结果表明,通过增强子A由NF-κB诱导的反式激活对含有两个NF-κB结合位点的HLA-A基因座最为重要。虽然HLA-B的增强子A仅含有一个NF-κB结合位点(κB1),但NF-κB仍有适度的反式激活作用。由于HLA-F虽然也有一个NF-κB结合位点但其KB2位点缺乏蛋白质结合,因此不被NF-κB反式激活,所以HLA-B中通过κB1基序由NF-κB介导的反式激活很可能是由转录因子Spl与上游κB2位点的结合所促进的。因此,NF-κB对HLA I类基因的转录调控仅限于HLA-A和HLA-B基因座。

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