首页> 外文期刊>Nucleic Acids Research >INCREASING BINDING OF A TRANSCRIPTION FACTOR IMMEDIATELY DOWNSTREAM OF THE CAP SITE OF A CYTOMEGALOVIRUS GENE REPRESSES EXPRESSION
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INCREASING BINDING OF A TRANSCRIPTION FACTOR IMMEDIATELY DOWNSTREAM OF THE CAP SITE OF A CYTOMEGALOVIRUS GENE REPRESSES EXPRESSION

机译:转录因子的结合立即降低了巨细胞病毒基因帽位的表达

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摘要

A closely related family of ubiquitous DNA binding proteins, called MDBP, binds with high affinity to two 14 base pair (bp) sites within the human cytomegalovirus immediate early gene 1 (CMV IE1) enhancer and with low affinity to one site beginning 5 bp downstream of the CMV IE1 transcription start point (+5 site). Unlike several cap position downstream MDBP sites in mammalian genes, these MDBP sites do not require cytosine methylation for optimal binding, Mutation of one of the enhancer MDBP sites to prevent MDBP recognition modestly increased the function of a neighboring CREB binding site in a transient transfection assay in the context of one promoter construct, A much larger effect on reporter gene expression (a 10-fold reduction) was seen when the low affinity MDBP recognition sequence at position +5 was converted to a high affinity site in a plasmid containing the CMV IE1 promoter upstream of the reporter gene, Evidence that the increased binding of MDBP at the mutant site is largely responsible for the observed results was provided by transfection experiments with this high affinity MDBP +5 site re-mutated to a non-binding site and by in vitro transcription assays.
机译:一个紧密相关的无处不在的DNA结合蛋白家族,称为MDBP,与人类巨细胞病毒即早基因1(CMV IE1)增强子中的两个14个碱基对(bp)位点具有高亲和力,而与下游5 bp开始的一个位点具有低亲和力CMV IE1转录起始点(+5位)。与哺乳动物基因中几个帽位下游的MDBP位点不同,这些MDBP位点不需要胞嘧啶甲基化即可实现最佳结合。在瞬时转染测定中,增强MDMD位点之一的突变可阻止MDBP的识别,从而适度增加了相邻CREB结合位点的功能在一个启动子构建体的背景下,当在包含CMV IE1的质粒中将位置+5处的低亲和力MDBP识别序列转换为高亲和力位点时,发现对报告基因表达的影响更大(降低了10倍)报告基因上游的启动子启动子,MDBP在突变位点的结合增加是观察结果的主要证据是通过将高亲和力MDBP +5位点重新突变为非结合位点的转染实验提供的。体外转录测定。

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