首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Induction of the Ly-6A/E gene by interferon alpha/beta and gamma requires a DNA element to which a tyrosine-phosphorylated 91-kDa protein binds.
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Induction of the Ly-6A/E gene by interferon alpha/beta and gamma requires a DNA element to which a tyrosine-phosphorylated 91-kDa protein binds.

机译:干扰素α/β和γ诱导Ly-6A / E基因需要与酪氨酸磷酸化的91-kDa蛋白结合的DNA元件。

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摘要

The murine Ly-6A/E gene is transcriptionally induced in cells exposed to interferon alpha/beta or gamma (IFN-alpha/beta or IFN-gamma). Analysis of the 5' flanking sequence using reporter plasmids that contain upstream elements of the Ly-6E gene has previously identified an approximately 850-base-pair IFN-responsive region that lacked an IFN-alpha-stimulated response element (ISRE), the element present and required for an IFN-alpha response of a number of genes. Analysis by deletion and stable transfection of the IFN-responsive region of the Ly-6E promoter has defined an 80-base-pair region containing an IFN-gamma activation site (GAS) but no ISRE that allows IFN-gamma and IFN-alpha inducibility of the Ly-6E gene. As tested by specific antiserum, a 91-kDa protein known to be activated in IFN-alpha- or IFN-gamma-treated cells binds to the GAS element from the Ly-6E promoter. The 91-kDa protein exists as an inactive cytoplasmic precursor and depends on tyrosine phosphorylation for its activation. Thus the same 91-kDa protein appears to act in the signal transduction pathways of both types of IFN for the Ly-6-A/E gene.
机译:在暴露于干扰素α/β或γ(IFN-α/β或IFN-γ)的细胞中,鼠Ly-6A / E基因被转录诱导。使用含有Ly-6E基因上游元件的报告质粒对5'侧翼序列进行分析,先前已鉴定出约850个碱基对的IFN反应区域,该区域缺少IFN-α刺激的反应元件(ISRE)。存在并且是许多基因的IFN-α应答所必需的。通过删除和稳定转染Ly-6E启动子的IFN反应区的分析确定了一个80个碱基对的区域,其中包含IFN-γ激活位点(GAS),但没有ISRE允许IFN-γ和IFN-α诱导Ly-6E基因。通过特定的抗血清测试,已知在IFN-α或IFN-γ处理的细胞中被激活的91-kDa蛋白与Ly-6E启动子的GAS元件结合。 91-kDa蛋白以无活性的细胞质前体形式存在,并依赖酪氨酸磷酸化来激活。因此,相同的91-kDa蛋白似乎在Ly-6-A / E基因的两种类型的IFN的信号转导途径中起作用。

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