首页> 外文期刊>Molecular and Cellular Biology >The intracisternal A-particle upstream element interacts with transcription factor YY1 to activate transcription: pleiotropic effects of YY1 on distinct DNA promoter elements.
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The intracisternal A-particle upstream element interacts with transcription factor YY1 to activate transcription: pleiotropic effects of YY1 on distinct DNA promoter elements.

机译:颅内A粒子上游元素与转录因子YY1相互作用以激活转录:YY1对不同DNA启动子元素的多效作用。

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Murine intracisternal A-particle long terminal repeats contain an intracisternal A-particle upstream enhancer (IUE) element that binds to a 65-kDa IUE binding protein (IUEB) present in both undifferentiated F9 embryonal carcinoma cells and differentiated parietal endoderm-like PYS-2 cells. This IUE element confers a CpG methylation-sensitive IUEB binding and enhancer activity. Using gel retardation, methylation interference, CpG methylation sensitivity binding, and cotransfection assays, we have now identified the 65-kDa IUEB as YY1 (also called NF-E1, delta, or UCRBP), a zinc finger protein related to the Krüppel family. YY1 binds to a number of similar but distinct DNA motifs, and cotransfection assays indicate that these motifs have different enhancer potentials in PYS-2 cells. The relative strengths of these elements are as follows: IUE > kappa E3' from the human immunoglobulin kappa light-chain 3' enhancer > upstream conserved region from the Moloney murine leukemia virus promoter. Results of DNA binding assays suggest that the differences in enhancer potentials are due to the different binding affinities of YY1 to the various motifs and the binding of two other transcription factors to the IUE sequence.
机译:小鼠脑池内A颗粒长末端重复序列包含一个脑池内A颗粒上游增强子(IUE)元件,该元件与未分化的F9胚胎癌细胞和分化的壁内胚层样PYS-2中均存在的65 kDa IUE结合蛋白(IUEB)结合细胞。此IUE元素赋予CpG甲基化敏感性IUEB结合和增强子活性。使用凝胶阻滞,甲基化干扰,CpG甲基化敏感性结合和共转染测定,我们现在已将65 kDa IUEB鉴定为YY1(也称为NF-E1,δ或UCRBP),这是与Krüppel家族相关的锌指蛋白。 YY1与许多相似但截然不同的DNA基序结合,共转染实验表明这些基序在PYS-2细胞中具有不同的增强子电位。这些元素的相对强度如下:IUE>来自人免疫球蛋白Kappa轻链3'增强子的Kappa E3'> Moloney鼠白血病病毒启动子的上游保守区。 DNA结合测定的结果表明,增强子电位的差异是由于YY1与各种基序的结合亲和力不同以及两个其他转录因子与IUE序列的结合所致。

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