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非洲爪蟾TFIIIA DNA结合结构域的剖析。5S RNA基因片段与含有三个、四个或五个锌指结构域的TFIIIA N端片段之间特异性复合物的定量DNase I足迹分析。

Dissection of the DNA-binding domain of Xenopus laevis TFIIIA. Quantitative DNase I footprinting analysis of specific complexes between a 5 S RNA gene fragment and N-terminal fragments of TFIIIA containing three, four or five zinc-finger domains.

作者信息

Hansen P K, Christensen J H, Nyborg J, Lillelund O, Thøgersen H C

机构信息

Department of Chemistry, University of Aarhus, Denmark.

出版信息

J Mol Biol. 1993 Sep 20;233(2):191-202. doi: 10.1006/jmbi.1993.1499.

Abstract

Recombinant zinc finger proteins corresponding to N-terminal fragments of Xenopus laevis transcription factor IIIA (TFIIIA) comprising three, four and five fingers produced in Escherichia coli as cleavable hybrid proteins were shown to form specific stoichiometric complexes with DNA fragments containing the internal control region (ICR) of a 5 S RNA gene. The ordered set of DNase I footprints of each of the three proteins on the ICR comprise a nested set of footprints extending upstream from its 3' end (position +96 relative to start of the mature transcript) 20 bp, 20 bp or 34 bp into the ICR, respectively. Quantitative analysis of the footprinting data provided firm evidence that the DNase I footprint, and hence the structure, of the authentic TFIIIA:ICR complex in this region is fully and precisely accounted for by the N-terminal three fingers binding within the +77 to +96 region plus the pair of fingers 4 and 5, both required to extend the footprint upwards from the +77 to the +63 position. A structural interpretation of this set of new footprinting data in view of previous results and data is presented and discussed in terms of a refined model in which the protein-DNA interaction between the ICR and the three N-terminal fingers corresponds closely to that observed in the homologous three-finger zif268:DNA complex, whereas the basic mode of protein-DNA interaction, in which the pair of fingers 4 and 5 is engaged in forming the TFIIIA:ICR complex is of an entirely different, albeit not yet understood nature. To allow assessment of our model in terms of potential specificity-determining H-bonding patterns, a molecular model of the complex between the three-finger TFIIIA fragment and the ICR was constructed, using the zif268:DNA co-ordinates. Eight out of the nine amino acid residues, which according to our model are suitably located for forming hydrogen bonds with the bases, are potential H-bond acceptors or donors.

摘要

在大肠杆菌中作为可切割杂合蛋白产生的、对应于非洲爪蟾转录因子IIIA(TFIIIA)N端片段(包含三个、四个和五个锌指)的重组锌指蛋白,被证明能与含有5S RNA基因内部控制区(ICR)的DNA片段形成特定的化学计量复合物。这三种蛋白在ICR上的有序脱氧核糖核酸酶I足迹集分别包含一组嵌套的足迹,从其3'端(相对于成熟转录本起始位置为+96)向上游延伸20bp、20bp或34bp进入ICR。对足迹数据的定量分析提供了确凿证据,表明该区域真实的TFIIIA:ICR复合物的脱氧核糖核酸酶I足迹以及结构,完全且精确地由结合在+77至+96区域内的N端三个锌指以及4和5这一对锌指来解释,这两个锌指都是将足迹从+77向上延伸至+63位置所必需的。鉴于先前的结果和数据,对这组新的足迹数据进行了结构解释,并根据一个改进模型进行了呈现和讨论。在该模型中,ICR与三个N端锌指之间的蛋白质 - DNA相互作用与在同源的三锌指zif268:DNA复合物中观察到的相互作用密切对应,而4和5这一对锌指参与形成TFIIIA:ICR复合物的蛋白质 - DNA相互作用基本模式则具有完全不同的性质,尽管尚未被理解。为了根据潜在的决定特异性的氢键模式评估我们的模型,利用zif268:DNA坐标构建了三锌指TFIIIA片段与ICR之间复合物的分子模型。根据我们的模型,九个氨基酸残基中有八个位置合适,可与碱基形成氢键,它们都是潜在的氢键受体或供体。

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