Thanos D, Gregoriou M, Stravopodis D, Liapaki K, Makatounakis T, Papamatheakis J
Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology, Crete, Greece.
Nucleic Acids Res. 1993 Dec 25;21(25):6010-9. doi: 10.1093/nar/21.25.6010.
The 5' proximal region of the E beta gene was studied with respect to B lymphoid expression and responsiveness to cytokines, revealing a complex array of general and cell type specific cis-elements and factors. Full lymphoid activity and response to interferon-gamma (IFN-gamma) is generated by the concerted action of the MHC boxes (H, X and Y) and additional elements. Combinatorial interactions between elements and their cognate factors are indicated by several lines of evidence. Thus, mutations within the X box in the promoter context are strongly deleterious to both B lymphoid activity and IFN-gamma regulation. However, the X box alone has minimal lymphoid activity upon heterologous promoters. Data from deletion, insertion and site directed mutagenesis demonstrate that sequences extending approximately 35 bp 5' of the X box (designated as Cytokine Response Sequence--CRS) have a dual role: they are required for cytokine-regulated expression as well as serving as an enhancer element for cell-specific constitutive expression. A region that carries X and CRS permits both lymphoid activity and IFN-gamma response. In contrast, sequences that include X and the downstream Y box are constitutively active in all cell types tested. Combination of the sequences both upstream and downstream of the X box results in a tissue-specific and cytokine-regulated enhancer of full strength. In vivo competition studies show that titratable trans-acting factors, shared by Class I and Class II promoters, mediate the CRS-dependent IFN-gamma response. We report here the identification of novel nuclear complexes that bind to the CRS and recognize sites which correlate with its negative or positive elements. One of these complexes is present in B lymphoid cells only. Three other CRS complexes that are upregulated by either IFN-alpha and IFN-gamma are competed by a non-Class II, IFN-alpha stimulated response element (ISRE), providing evidence for the functional interconnection of these cytokines.
对Eβ基因的5'近端区域进行了关于B淋巴细胞表达和细胞因子反应性的研究,揭示了一系列复杂的通用和细胞类型特异性顺式元件及因子。主要组织相容性复合体(MHC)框(H、X和Y)以及其他元件的协同作用产生了完全的淋巴细胞活性和对干扰素-γ(IFN-γ)的反应。多条证据表明元件与其相关因子之间存在组合相互作用。因此,启动子环境中X框内的突变对B淋巴细胞活性和IFN-γ调节均有强烈的有害影响。然而,单独的X框在异源启动子上具有最小的淋巴细胞活性。缺失、插入和定点诱变的数据表明,X框5'端大约延伸35 bp的序列(称为细胞因子反应序列——CRS)具有双重作用:它们是细胞因子调节表达所必需的,同时还作为细胞特异性组成型表达的增强子元件。携带X和CRS的区域允许淋巴细胞活性和IFN-γ反应。相比之下,包括X和下游Y框的序列在所有测试的细胞类型中均组成性活跃。X框上下游序列的组合产生了一个具有完全强度的组织特异性和细胞因子调节的增强子。体内竞争研究表明,I类和II类启动子共有的可滴定反式作用因子介导了CRS依赖性IFN-γ反应。我们在此报告鉴定了与CRS结合并识别与其阴性或阳性元件相关位点的新型核复合物。其中一种复合物仅存在于B淋巴细胞中。另外三种被IFN-α和IFN-γ上调的CRS复合物被非II类IFN-α刺激反应元件(ISRE)竞争,这为这些细胞因子的功能相互联系提供了证据。