Aird W C, Parvin J D, Sharp P A, Rosenberg R D
Department of Biology, Massachusetts Institute of Technology, Cambridge 02136.
J Biol Chem. 1994 Jan 14;269(2):883-9.
The core promoters of the rat platelet factor 4 (PF4), mouse erythropoietin and chicken beta globin genes contain a GATA motif in place of the consensus TATAAA site. In the case of the PF4 gene, this site has been shown to play a critical role in restricting transcription to the megakaryocyte lineage. In order to understand the mechanism of tissue specificity, we investigated the function of the GATA box-containing promoters in vitro. Our studies show that the TATA-binding protein of TFIID is required for initiation of transcription from the GATA box-containing promoters. GATA-1 interacts with the core promoter GATA motif and inhibits generation of preinitiation complexes. The functional significance of the inhibition of preinitiation complexes is supported by in vitro transcription assays in which transcription from the PF4 and erythropoietin core promoters is suppressed by GATA-1. We also demonstrate that GATA-2 inhibits initiation of transcription from the PF4 core promoter. Based on these results, we propose a model in which repression of PF4 expression in nonmegakaryocytes is mediated, in part, by competition between GATA-binding proteins and basal factors for the core promoter.
大鼠血小板因子4(PF4)、小鼠促红细胞生成素和鸡β珠蛋白基因的核心启动子含有一个GATA基序,取代了共有TATAAA位点。就PF4基因而言,该位点已被证明在将转录限制于巨核细胞谱系中起关键作用。为了理解组织特异性的机制,我们在体外研究了含GATA框启动子的功能。我们的研究表明,TFIID的TATA结合蛋白是从含GATA框启动子起始转录所必需的。GATA-1与核心启动子GATA基序相互作用,并抑制起始前复合物的形成。起始前复合物受抑制的功能意义得到了体外转录分析的支持,在该分析中,PF4和促红细胞生成素核心启动子的转录被GATA-1抑制。我们还证明GATA-2抑制PF4核心启动子的转录起始。基于这些结果,我们提出了一个模型,其中非巨核细胞中PF4表达的抑制部分是由GATA结合蛋白和基础因子对核心启动子的竞争介导的。