首页> 美国卫生研究院文献>Nucleic Acids Research >Reciprocal regulation of expression of the human adenosine 5′-triphosphate binding cassette sub-family A transporter 2 (ABCA2) promoter by the early growth response-1 (EGR-1) and Sp-family transcription factors
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Reciprocal regulation of expression of the human adenosine 5′-triphosphate binding cassette sub-family A transporter 2 (ABCA2) promoter by the early growth response-1 (EGR-1) and Sp-family transcription factors

机译:早期生长应答1(EGR-1)和Sp家族转录因子对人腺苷5-三磷酸结合盒亚家族A转运蛋白2(ABCA2)启动子表达的相互调节

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摘要

The human ABCA2 transporter gene encodes a member of a large family of ATP-binding proteins that transport a variety of macromolecules across biological membranes. We have performed luciferase reporter gene assays with promoter constructs comprising the 5′-flanking region to identify cis-regulatory DNA elements and have mapped the minimal promoter region to 321 bp upstream of the translation start site. We have discovered a functional role for two GC-boxes located in the proximal promoter of the ABCA2 gene that contain overlapping sites for the EGR-1 and Sp1 transcription factors. We observed that oligonucleotides containing overlapping EGR-1/Sp1 sites bind the Sp1, Sp3 and Sp4 transcription factors. When BE(2)-M17 cells were treated with phorbol 12-myristate 13-acetate, we observed inducible expression and binding of the EGR-1 transcription factor to the two GC-boxes. Transfection of Sp1, Sp3 or Sp4 expression constructs into Drosophila S2 induced a dose-dependent increase in transcriptional activation of the ABCA2 promoter, but transfection of EGR-1 alone failed to activate transcription. When increasing amounts of EGR-1 were transfected into the BE(2)-M17 neuroblastoma cells we observed a dose-dependent decrease in expression of the ABCA2 promoter, although expression of the endogenous ABCA2 gene increased following transfection of EGR-1.
机译:人ABCA2转运蛋白基因编码一大类ATP结合蛋白的成员,该蛋白可跨生物膜转运各种大分子。我们已经用包含5'侧翼区的启动子构建体进行了荧光素酶报告基因分析,以鉴定顺式调控DNA元件,并将最小启动子区定位到翻译起始位点上游321 bp。我们发现位于ABCA2基因近端启动子中的两个GC框具有功能性作用,其中两个框包含EGR-1和Sp1转录因子的重叠位点。我们观察到包含重叠的EGR-1 / Sp1位点的寡核苷酸结合Sp1,Sp3和Sp4转录因子。当用佛波醇12-肉豆蔻酸酯13-乙酸酯处理BE(2)-M17细胞时,我们观察到了EGR-1转录因子与两个GC-box的诱导表达和结合。 Sp1,Sp3或Sp4表达构建体转染到果蝇S2中会诱导ABCA2启动子的转录激活呈剂量依赖性增加,但仅EGR-1的转染未能激活转录。当越来越多的EGR-1转染到BE(2)-M17神经母细胞瘤细胞中时,我们观察到了ABCA2启动子表达的剂量依赖性降低,尽管内源ABCA2基因的表达在EGR-1转染后增加了。

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