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Sp1和Sp3调节人类载脂蛋白B编辑酶催化多肽样蛋白3G(APOBEC3G)基因的基础转录。

Sp1 and Sp3 regulate basal transcription of the human APOBEC3G gene.

作者信息

Muckenfuss Heide, Kaiser Julia K, Krebil Erika, Battenberg Marion, Schwer Christina, Cichutek Klaus, Münk Carsten, Flory Egbert

机构信息

Division of Medical Biotechnology, Paul-Ehrlich-Institut, Paul-Ehrlich-Strasse 51-59, D-63225 Langen, Germany.

出版信息

Nucleic Acids Res. 2007;35(11):3784-96. doi: 10.1093/nar/gkm340. Epub 2007 May 21.

DOI:10.1093/nar/gkm340
PMID:17517765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1920263/
Abstract

APOBEC3G (A3G), a member of the recently discovered family of human cytidine deaminases, is expressed in peripheral blood lymphocytes and has been shown to be active against HIV-1 and other retroviruses. To gain new insights into the transcriptional regulation of this restriction factor, we cloned and characterized the promoter region of A3G. Transcriptional start sites were identified by 5'-rapid amplification of cDNA ends analysis. Luciferase reporter assays demonstrated that a 1025 bp A3G promoter sequence (from -959 to +66 relative to the major transcriptional start site) displayed constitutive promoter activity. In T cells, the A3G promoter was not inducible by mitogenic stimulation, interferon treatment or expression of HIV-1 proteins. Using a series of 5' deletion promoter constructs in luciferase reporter assays, we identified a 180 bp region that was sufficient for full promoter activity. Transcriptional activity of this A3G core promoter was dependent on a GC-box (located at position -87/-78 relative to the major transcriptional start site) and was abolished after mutation of this DNA element. Electrophoretic mobility shift assays and chromatin immunoprecipitation assays demonstrated that the identified GC-box represented a binding site for the ubiquitous transcription factors specificity protein (Sp) 1 and Sp3.

摘要

载脂蛋白B mRNA编辑酶催化多肽样蛋白3G(APOBEC3G或A3G)是最近发现的人类胞苷脱氨酶家族的成员之一,在外周血淋巴细胞中表达,并已证明对HIV-1和其他逆转录病毒具有活性。为了深入了解这种限制因子的转录调控机制,我们克隆并鉴定了A3G的启动子区域。通过5'-cDNA末端快速扩增分析确定转录起始位点。荧光素酶报告基因检测表明,一段1025bp的A3G启动子序列(相对于主要转录起始位点从-959到+66)具有组成型启动子活性。在T细胞中,A3G启动子不受促有丝分裂刺激、干扰素处理或HIV-1蛋白表达的诱导。通过荧光素酶报告基因检测中一系列5'缺失启动子构建体,我们鉴定出一个180bp的区域,该区域足以实现完整的启动子活性。该A3G核心启动子的转录活性依赖于一个GC盒(相对于主要转录起始位点位于-87/-78位置),并且在该DNA元件发生突变后被消除。电泳迁移率变动分析和染色质免疫沉淀分析表明,鉴定出的GC盒代表了普遍存在的转录因子特异性蛋白(Sp)1和Sp3的结合位点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/42837ca34f76/gkm340f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/4a132a582c5f/gkm340f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/ebbe30731838/gkm340f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/2d5221f4f52c/gkm340f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/e1cdd1e5f5cb/gkm340f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/d26e1e6280f5/gkm340f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/a9bb6aab806a/gkm340f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/42837ca34f76/gkm340f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/4a132a582c5f/gkm340f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/ebbe30731838/gkm340f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/2d5221f4f52c/gkm340f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/e1cdd1e5f5cb/gkm340f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/d26e1e6280f5/gkm340f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/a9bb6aab806a/gkm340f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c885/1920263/42837ca34f76/gkm340f7.jpg

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