Yu M, Yang X Y, Schmidt T, Chinenov Y, Wang R, Martin M E
Department of Biochemistry, University of Missouri at Columbia, Columbia, Missouri 65212, USA.
J Biol Chem. 1997 Nov 14;272(46):29060-7. doi: 10.1074/jbc.272.46.29060.
Many eukaryotic RNA polymerase II promoters contain initiator elements which direct accurate transcription in a TATA-independent manner. The PEA3/Ets-binding site (PEA3/EBS) is a common enhancer element in eukaryotic genes and is also found near the transcriptional start sites of many TATA-less promoters. We demonstrate that two PEA3/EBSs driving expression of the luciferase reporter gene, function as a minimal transcriptional initiator element. Maximal levels of transcription was achieved when two PEA3/EBSs, in either orientation, were located on the same face of the DNA helix, and the sites could be separated by up to three helical turns. In vitro transcription start sites directed by PEA3/EBS elements were clustered on either side of the upstream PEA3/EBS and were abolished by immunodepletion of GA-binding protein (GABP) from FM3A cell nuclear extracts. In vivo, co-transfection of GABPalpha and GABPbeta expression vectors enhanced reporter gene expression driven from PEA3/EBS initiator elements. Like other initiator elements, the PEA3/EBS elements were activated synergistically by upstream Sp1-binding sites. Thus, our results establish GABP as both a transcriptional activator factor and as an initiator factor.
许多真核生物RNA聚合酶II启动子包含起始元件,这些元件以不依赖TATA的方式指导精确转录。PEA3/Ets结合位点(PEA3/EBS)是真核基因中常见的增强子元件,在许多无TATA启动子的转录起始位点附近也能发现。我们证明,驱动荧光素酶报告基因表达的两个PEA3/EBS作为最小转录起始元件发挥作用。当两个PEA3/EBS以任意方向位于DNA螺旋的同一面上时,可实现最大转录水平,且两个位点之间最多可相隔三个螺旋圈。由PEA3/EBS元件指导的体外转录起始位点聚集在上游PEA3/EBS的两侧,并且通过从FM3A细胞核提取物中免疫去除GA结合蛋白(GABP)而被消除。在体内,共转染GABPα和GABPβ表达载体可增强由PEA3/EBS起始元件驱动的报告基因表达。与其他起始元件一样,PEA3/EBS元件被上游Sp1结合位点协同激活。因此,我们的结果确立了GABP既是转录激活因子又是起始因子。