Kuhen K L, Samuel C E
Interdepartmental Program of Biochemistry and Molecular Biology, University of California, Santa Barbara, California, 93106, USA.
Virology. 1997 Jan 6;227(1):119-30. doi: 10.1006/viro.1996.8306.
The RNA-dependent protein kinase (PKR) is inducible by interferon (IFN) and is implicated in the antiviral and antiproliferative actions of IFN. We have now isolated human genomic clones that contain the promoter region required for transcription of the Pkr gene. Transient transfection analyses, using chloramphenicol acetyltransferase (CAT) as the reporter in constructs possessing various 5'-flanking fragments of the Pkr gene, led to the identification of a functional TATA-less promoter that directed IFN-inducible transcription of CAT. Sequence determination and deletion analysis of the promoter region revealed an element (5'GGAAAACGAAACT3') involved in IFN inducibility that corresponds to the consensus sequence of the IFN-stimulated response element (ISRE). Comparison of the promoter sequence of the human Pkr gene to that of the mouse homolog identified a novel element (5'GGGAAGGCGGAGTCC3') immediately upstream of the ISRE element which so far is unique to the human and mouse Pkr gene promoters. We have designated this new motif as KCS, for kinase conserved sequence. Deletion and substitution mutants of the Pkr promoter region showed that the ISRE element was required for transcriptional induction by type I IFN, whereas the KCS motif increased promoter activity mediated by the ISRE. Additional potential regulatory cis-elements were identified in the human Pkr promoter that are commonly associated with growth control regulation and differentiation. Other than the ISRE and novel KCS elements, the overall organization of potential binding sites for transcription factors was not well conserved between the IFN-inducible promoters of the human and mouse Pkr genes. The strict conservation of sequence, distance, and position of KCS, relative to ISRE, together with mutagenesis results, suggest an important functional role for the newly recognized KCS motif.
RNA依赖性蛋白激酶(PKR)可被干扰素(IFN)诱导,并参与IFN的抗病毒和抗增殖作用。我们现已分离出包含Pkr基因转录所需启动子区域的人类基因组克隆。使用氯霉素乙酰转移酶(CAT)作为报告基因,对含有Pkr基因各种5'侧翼片段的构建体进行瞬时转染分析,从而鉴定出一个功能性的无TATA启动子,该启动子可指导CAT的IFN诱导型转录。对启动子区域进行序列测定和缺失分析,发现了一个与IFN诱导性有关的元件(5'GGAAAACGAAACT3'),它与IFN刺激反应元件(ISRE)的共有序列相对应。将人类Pkr基因的启动子序列与小鼠同源物的启动子序列进行比较,在ISRE元件上游紧邻处发现了一个新元件(5'GGGAAGGCGGAGTCC3'),该元件迄今为止是人类和小鼠Pkr基因启动子所特有的。我们将这个新基序命名为KCS,即激酶保守序列。Pkr启动子区域的缺失和替代突变体表明,I型IFN转录诱导需要ISRE元件,而KCS基序可增强由ISRE介导的启动子活性。在人类Pkr启动子中还鉴定出了其他一些潜在的调控顺式元件,它们通常与生长控制调节和分化相关。除了ISRE和新的KCS元件外,人类和小鼠Pkr基因的IFN诱导型启动子之间,转录因子潜在结合位点的总体组织情况并不保守。KCS相对于ISRE在序列、距离和位置上的严格保守性,以及诱变结果,表明新识别出的KCS基序具有重要的功能作用。