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对位于黑腹果蝇hsp70启动子中TATA元件下游的核心启动子序列的分析。

Analysis of core promoter sequences located downstream from the TATA element in the hsp70 promoter from Drosophila melanogaster.

作者信息

Wu C H, Madabusi L, Nishioka H, Emanuel P, Sypes M, Arkhipova I, Gilmour D S

机构信息

Center for Gene Regulation, Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.

出版信息

Mol Cell Biol. 2001 Mar;21(5):1593-602. doi: 10.1128/MCB.21.5.1593-1602.2001.

Abstract

TFIID recognizes multiple sequence elements in the hsp70 promoter of Drosophila. Here, we investigate the function of sequences downstream from the TATA element. A mutation in the initiator was identified that caused an eightfold reduction in binding of TFIID and a fourfold reduction in transcription in vitro. Another mutation in the +24 to +29 region was somewhat less inhibitory, but a mutation in the +14 to +19 region had essentially no effect. The normal promoter and the mutants in the initiator and the +24 to +29 region were transformed into flies by P element-mediated transformation. The initiator mutation reduced expression an average of twofold in adult flies, whereas the mutation in the +24 to +29 region had essentially no effect. In contrast, a promoter combining the two mutations was expressed an average of sixfold less than the wild type. The results suggest that the initiator and the +24 to +29 region could serve overlapping functions in vivo. Protein-DNA cross-linking was used to identify which subunits of TFIID contact the +24 to +29 region and the initiator. No specific subunits were found to cross-link to the +24 to +29 region. In contrast, the initiator cross-linked exclusively to dTAF230. Remarkably, dTAF230 cross-links approximately 10 times more efficiently to the nontranscribed strand than to the transcribed strand at the initiator.

摘要

TFIID可识别果蝇hsp70启动子中的多个序列元件。在此,我们研究TATA元件下游序列的功能。我们鉴定出起始子中的一个突变,该突变导致TFIID结合减少八倍,体外转录减少四倍。+24至+29区域的另一个突变抑制作用稍小,但+14至+19区域的突变基本没有影响。通过P元件介导的转化,将正常启动子以及起始子和+24至+29区域的突变体导入果蝇。起始子突变使成年果蝇中的表达平均降低两倍,而+24至+29区域的突变基本没有影响。相反,结合了这两个突变的启动子的表达比野生型平均低六倍。结果表明,起始子和+24至+29区域在体内可能具有重叠功能。采用蛋白质-DNA交联法来鉴定TFIID的哪些亚基与+24至+29区域和起始子发生接触。未发现有特定亚基与+24至+29区域发生交联。相反,起始子仅与dTAF230发生交联。值得注意的是,在起始子处,dTAF230与非转录链的交联效率比与转录链的交联效率高约10倍。

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