Israel A, Kimura A, Fournier A, Fellous M, Kourilsky P
Nature. 1986;322(6081):743-6. doi: 10.1038/322743a0.
The expression of class I transplantation antigens encoded in the major histocompatibility complex (H-2 in mouse, HLA in man) can be induced by alpha-, beta- and gamma-interferons. Both transcriptional and post-transcriptional mechanisms have been postulated. Recently, a common sequence has been found in the promoter region of several human genes responsive to IFN-alpha. The promoters of H-2Kb and several other mouse class I genes contain a similar interferon response sequence. We show here, in a transient assay, that the H-2Kb promoter can be induced by all three types of interferon and that the interferon response sequence is necessary for induction to occur. However, the response sequence is active only when associated with a functional enhancer sequence which we have recently identified in the promoter of H-2Kb and other class I genes. The combination of these two sequences can render a heterologous promoter responsive to interferon, irrespective of its orientation relative to the cap site.
主要组织相容性复合体(小鼠为H - 2,人类为HLA)编码的I类移植抗原的表达可由α、β和γ干扰素诱导。转录和转录后机制都已被提出。最近,在几个对IFN - α有反应的人类基因的启动子区域发现了一个共同序列。H - 2Kb和其他几个小鼠I类基因的启动子含有类似的干扰素反应序列。我们在此通过瞬时分析表明,H - 2Kb启动子可被所有三种类型的干扰素诱导,且干扰素反应序列是诱导发生所必需的。然而,该反应序列仅在与我们最近在H - 2Kb和其他I类基因启动子中鉴定出的功能性增强子序列相关联时才具有活性。这两个序列的组合可使异源启动子对干扰素产生反应,而不论其相对于帽位点的方向如何。