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首页> 外文期刊>The Biochemical Journal >Functional analysis of the promoter region of the human phosphotyrosine phosphatase activator gene: Yin Yang 1 is essential for core promoter activity.
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Functional analysis of the promoter region of the human phosphotyrosine phosphatase activator gene: Yin Yang 1 is essential for core promoter activity.

机译:人磷酸酪氨酸磷酸酶激活基因的启动子区域的功能分析:阴阳1对于核心启动子活性至关重要。

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The phosphotyrosine phosphatase activator (PTPA) has been isolated as an in vitro regulator of protein phosphatase 2A. Human PTPA is encoded by a single gene, the structure and chromosomal localization of which have been determined in our previous work. Here we describe the further isolation, sequencing and functional characterization of the PTPA promoter region. In agreement with its ubiquitous expression, the PTPA promoter displays several characteristics of housekeeping genes: it lacks both a TATA-box and a CAAT-box, it is very GC-rich and it contains an unmethylated CpG island surrounding the transcription initiation site. Transient transfection experiments in different cell types with several truncated chimaeric luciferase reporter gene plasmids revealed the importance of the region between positions -67 and -39 for basal promoter activity. This region coincides remarkably well with the determined CpG island. Further analysis of this region demonstrated the presence of a Yin Yang 1 (YY1) binding motif at positions -52 to -44. Binding of YY1 to this sequence is demonstrated in bandshift and DNase I footprinting experiments. Another YY1 binding motif is found in the 5' untranslated region, at positions +27 to +35. Mutations in either of these sites, abolishing YY1 binding in vitro, have differential effects on promoter activity. Point mutations in both sites completely abolish promoter activity. Moreover, induction of promoter activity by co-transfection with a YY1 expression plasmid is fully dependent upon the presence of both intact YY1 binding sites. Thus YY1 apparently mediates basal transcription of the human PTPA gene through two binding sites within its proximal promoter.
机译:磷酸酪氨酸磷酸酶激活剂(PTPA)已被分离为蛋白质磷酸酶2A的体外调节剂。人PTPA由单个基因编码,其结构和染色体定位已在我们先前的工作中确定。在这里,我们描述了PTPA启动子区域的进一步分离,测序和功能表征。与它的普遍表达相一致,PTPA启动子显示出管家基因的几个特征:它既没有TATA框又没有CAAT框,富含GC,并且在转录起始位点周围包含一个未甲基化的CpG岛。用几种截短的嵌合荧光素酶报告基因基因质粒在不同细胞类型中进行的瞬时转染实验揭示了-67和-39位之间的区域对于基础启动子活性的重要性。该区域与确定的CpG岛非常吻合。对该区域的进一步分析表明,在位置-52至-44处存在阴阳1(YY1)结合基序。在带移和DNase I足迹实验中证明了YY1与该序列的结合。在5'非翻译区的+27至+35位发现了另一个YY1结合基序。这些位点中的任何一个都在体外取消了YY1结合的突变,对启动子活性具有不同的影响。两个位点中的点突变完全消除了启动子活性。而且,通过与YY1表达质粒共转染诱导启动子活性完全取决于两个完整的YY1结合位点的存在。因此,YY1显然通过其近端启动子内的两个结合位点介导人PTPA基因的基础转录。

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