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转录起始由原生动物寄生虫溶组织内阿米巴的hgl5基因中的三个核心启动子元件控制。

Transcription initiation is controlled by three core promoter elements in the hgl5 gene of the protozoan parasite Entamoeba histolytica.

作者信息

Singh U, Rogers J B, Mann B J, Petri W A

机构信息

Department of Medicine, University of Virginia, Charlottesville, VA 22908, USA.

出版信息

Proc Natl Acad Sci U S A. 1997 Aug 5;94(16):8812-7. doi: 10.1073/pnas.94.16.8812.

Abstract

Entamoeba histolytica is a single cell eukaryote that is the etiologic agent of amoebic colitis. Core promoter elements of E. histolytica protein encoding genes include a TATA-like sequence (GTATTTAAAG/C) at -30, a novel element designated GAAC (GAACT) that has a variable location between TATA and the site of transcription initiation, and a putative initiator (Inr) element (AAAAATTCA) overlying the site of transcription initiation. The presence of three separate conserved sequences in a eukaryotic core promoter is unprecedented and prompted examination of their roles in regulating transcription initiation. Alterations of all three regions in the hgl5 gene decreased reporter gene activity with the greatest effect seen by mutation of the GAAC element. Positional analysis of the TATA box demonstrated that transcription initiated consistently 30-31 bases downstream of the TATA region. Mutation of either the TATA or GAAC elements resulted in the appearance of new transcription start sites upstream of +1 in the promoter of the hgl5 gene. Mutation of the Inr element resulted in no change in the site of transcription initiation; however, in the presence of a mutated TATA and GAAC regions, the Inr element controlled the site of transcription initiation. We conclude that all three elements play a role in determining the site of transcription initiation. The variable position of the GAAC element relative to the site of transcription initiation, and the multiple transcription initiations that resulted from its mutation, indicate that the GAAC element has an important and apparently novel role in transcriptional control in E. histolytica.

摘要

溶组织内阿米巴是一种单细胞真核生物,是阿米巴性结肠炎的病原体。溶组织内阿米巴蛋白质编码基因的核心启动子元件包括位于-30处的类似TATA的序列(GTATTTAAAG/C)、一个新元件GAAC(GAACT),其在TATA和转录起始位点之间的位置可变,以及一个覆盖转录起始位点的假定起始子(Inr)元件(AAAAATTCA)。真核生物核心启动子中存在三个独立的保守序列是前所未有的,这促使人们研究它们在调节转录起始中的作用。hgl5基因中所有三个区域的改变均降低了报告基因活性,其中GAAC元件突变的影响最大。TATA框的定位分析表明,转录在TATA区域下游30-31个碱基处一致起始。TATA或GAAC元件的突变导致hgl5基因启动子中+1上游出现新的转录起始位点。Inr元件的突变导致转录起始位点没有变化;然而,在存在突变的TATA和GAAC区域的情况下,Inr元件控制转录起始位点。我们得出结论,所有这三个元件在确定转录起始位点中都起作用。GAAC元件相对于转录起始位点的可变位置,以及其突变导致的多个转录起始,表明GAAC元件在溶组织内阿米巴的转录控制中具有重要且明显新颖的作用。

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