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首页> 外文期刊>Nucleic acids research >Characterization of the human β‐globin downstream promoter region
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Characterization of the human β‐globin downstream promoter region

机译:人类β-珠蛋白下游启动子区域的表征

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摘要

The human β‐globin gene is abundantly expressed specifically in adult erythroid cells. Stage‐specific transcription is regulated principally by promoter proximal cis‐regulatory elements. The basal promoter contains a non‐canonical TATA‐like motif as well as an initiator element. These two elements have been shown to interact with the TFII‐D complex. Here we show that in addition to the TATA and initiator elements, conserved E‐box motifs are located in the β‐globin downstream promoter. One of the E‐box motifs overlaps the initiator and this composite element interacts with USF1 and TFII‐I in vitro. Another E‐box, located 60 bp 3′ to the transcription initiation site, interacts with USF1 and USF2. Mutations of either the initiator or the downstream E‐box impair transcription of the β‐globin gene in vitro. Mutations of a putative NF‐E2‐binding site in the downstream promoter region do not affect transcription in vitro. USF1, USF2, TFII‐I and p45 can be crosslinked to a β‐globin promoter fragment in MEL cells in vivo, whereas only TFII‐I and USF2 crosslink to the β‐globin gene in K562 cells. The summary data demonstrate that in addition to the well‐characterized interactions of the TFII‐D complex with the basal promoter, E‐box motifs contribute to the efficient formation of transcription complexes on the adult β‐globin gene.
机译:人β-珠蛋白基因在成年红系细胞中大量表达。阶段特异性转录主要受启动子近端顺式调控元件调控。基础启动子包含非经典的TATA样基序以及启动子元件。已显示这两个元素与TFII-D复合体相互作用。在这里,我们表明,除了TATA和启动子元件外,保守的E-box基序也位于β-珠蛋白下游启动子中。 E-box主题之一与引发剂重叠,并且该复合元素在体外与USF1和TFII-I相互作用。另一个E-box位于转录起始位点3 bp处,与USF1和USF2相互作用。启动子或下游E-box的突变会在体外损害β-珠蛋白基因的转录。下游启动子区域假定的NF-E2结合位点的突变不会影响体外转录。 USF1,USF2,TFII-I和p45可以在MEL细胞中与体内的β-珠蛋白启动子片段交联,而只有TFII-1和USF2与K562细胞中的β-珠蛋白基因交联。汇总数据表明,除了TFII-D复合物与基础启动子的良好表征相互作用外,E-box基序还有助于在成人β-珠蛋白基因上有效形成转录复合物。

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