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本文引用的文献

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pH, EF-1alpha and the cytoskeleton.pH值、延伸因子1α与细胞骨架
Trends Cell Biol. 1996 May;6(5):168-71. doi: 10.1016/0962-8924(96)20013-3.
2
Transcription factor Sp1 is essential for early embryonic development but dispensable for cell growth and differentiation.转录因子Sp1对早期胚胎发育至关重要,但对细胞生长和分化并非必需。
Cell. 1997 May 16;89(4):619-28. doi: 10.1016/s0092-8674(00)80243-3.
3
Role of the stimulatory proteins Sp1 and Sp3 in the regulation of transcription of the rat pyruvate kinase M gene.刺激蛋白Sp1和Sp3在大鼠丙酮酸激酶M基因转录调控中的作用
Eur J Biochem. 1997 Apr 1;245(1):174-81. doi: 10.1111/j.1432-1033.1997.00174.x.
4
The ability of C/EBP beta but not C/EBP alpha to synergize with an Sp1 protein is specified by the leucine zipper and activation domain.亮氨酸拉链和激活结构域决定了C/EBPβ而非C/EBPα与Sp1蛋白协同作用的能力。
Mol Cell Biol. 1997 Apr;17(4):2038-47. doi: 10.1128/MCB.17.4.2038.
5
Sp3 is a bifunctional transcription regulator with modular independent activation and repression domains.Sp3是一种具有模块化独立激活和抑制结构域的双功能转录调节因子。
J Biol Chem. 1997 Feb 14;272(7):4021-6. doi: 10.1074/jbc.272.7.4021.
6
Involvement of the Sp3 transcription factor in induction of p21Cip1/WAF1 in keratinocyte differentiation.Sp3转录因子参与角质形成细胞分化过程中p21Cip1/WAF1的诱导。
J Biol Chem. 1997 Jan 10;272(2):1308-14. doi: 10.1074/jbc.272.2.1308.
7
The general transcription factors of RNA polymerase II.RNA聚合酶II的通用转录因子。
Genes Dev. 1996 Nov 1;10(21):2657-83. doi: 10.1101/gad.10.21.2657.
8
An inhibitor domain in Sp3 regulates its glutamine-rich activation domains.Sp3中的一个抑制结构域调节其富含谷氨酰胺的激活结构域。
EMBO J. 1996 Oct 15;15(20):5659-67.
9
The role of general initiation factors in transcription by RNA polymerase II.通用起始因子在RNA聚合酶II转录中的作用。
Trends Biochem Sci. 1996 Sep;21(9):327-35.
10
Transcriptional regulation of the SIS/PDGF-B gene in human osteosarcoma cells by the Sp family of transcription factors.转录因子Sp家族对人骨肉瘤细胞中SIS/PDGF-B基因的转录调控
J Biol Chem. 1996 May 17;271(20):11792-7. doi: 10.1074/jbc.271.20.11792.

不同的Sp1家族成员对人类延伸因子1A-1基因启动子的转录有不同影响。

Different Sp1 family members differentially affect transcription from the human elongation factor 1 A-1 gene promoter.

作者信息

Nielsen S J, Praestegaard M, Jorgensen H F, Clark B F

机构信息

Department of Biostructural Chemistry, Institute of Molecular and Structural Biology, University of Aarhus, Gustav Wieds Vej 10C, Forskerparken, Arhus, Denmark.

出版信息

Biochem J. 1998 Aug 1;333 ( Pt 3)(Pt 3):511-7. doi: 10.1042/bj3330511.

DOI:10.1042/bj3330511
PMID:9677307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1219611/
Abstract

The GC box is an important transcriptional regulatory element present in the promoters of many mammalian genes. In the present study we examine the effect of known GC-box-binding proteins on the promoter of the human elongation factor 1 A-1 (hEF1A-1) gene in human HeLa cells and Drosophila SL2 cells. In HeLa cells co-transfection with the GC-box-binding protein BTEB resulted in a 4-10-fold increase in hEF1A-1 promoter activity. This stimulation was dependent on a single GC box located between positions -69 and -50 of the promoter. Little or no effect was observed of other GC-box-binding proteins including Sp1, Sp3, Sp4 and BTEB2. In SL2 cells stimulation by Sp1 and Sp3 through the single GC box of the proximal promoter led to 13-fold and 21-fold increases respectively in promoter activity. Inclusion of further upstream sequences resulted in high levels of expression when Sp1 or Sp3 was co-transfected with the reporter plasmid. In this setting Sp1 stimulated transcription by 750-fold, whereas Sp3 was even more potent, yielding a 1150-fold stimulation. Mobility-shift assays performed with the promoter-proximal GC box demonstrated the binding of Sp1, Sp3 and Sp4 to this sequence. To our knowledge, the present study represents the first comparison of all known GC-box-binding proteins on a natural promoter.

摘要

GC框是许多哺乳动物基因启动子中存在的一种重要转录调控元件。在本研究中,我们检测了已知的GC框结合蛋白对人HeLa细胞和果蝇SL2细胞中人延伸因子1A-1(hEF1A-1)基因启动子的影响。在HeLa细胞中,与GC框结合蛋白BTEB共转染导致hEF1A-1启动子活性增加4至10倍。这种刺激依赖于位于启动子-69至-50位之间的单个GC框。未观察到其他GC框结合蛋白(包括Sp1、Sp3、Sp4和BTEB2)有明显影响。在SL2细胞中,Sp1和Sp3通过近端启动子的单个GC框进行刺激,分别导致启动子活性增加13倍和21倍。当Sp1或Sp3与报告质粒共转染时,加入更多上游序列会导致高水平表达。在这种情况下,Sp1刺激转录750倍,而Sp3的作用更强,产生1150倍的刺激。用启动子近端GC框进行的迁移率变动分析证明Sp1、Sp3和Sp4与该序列结合。据我们所知,本研究是对天然启动子上所有已知GC框结合蛋白的首次比较。