Spicuglia Salvatore, Kumar Sanjeev, Chasson Lionel, Payet-Bornet Dominique, Ferrier Pierre
Centre d'Immunologie de Marseille-Luminy (CIML), INSERM-CNRS-Université de la Méditerranée Case 906, 13288 Marseille cedex 09, France.
J Biochem Biophys Methods. 2004 May 31;59(2):189-94. doi: 10.1016/j.jbbm.2004.01.012.
Potassium permanganate (KMnO4) has widely been used in genomic footprinting assays to map unusual gene structures, including the melting DNA block in transcriptional elongation that results from promoter-proximal pausing of RNA polymerase (Pol) II complexes. Although it has been assumed that DNA-bound proteins do not protect underlying nucleic acids from KMnO4 modifications, we provide evidence herein that this chemical can readily be used to detect nuclear factor loading at a promoter when using optimized conditions. Moreover, by comparing parallel KMnO4 and dimethylsulfate (DMS) in vivo footprintings, we show that the utilization of KMnO4 in combination with another chemical probe maximizes the detection of factor occupancy at a DNA regulatory region, thus providing a better opportunity to define the actual profiles of DNA-protein contacts at given genomic sites in living cells.
高锰酸钾(KMnO4)已广泛应用于基因组足迹分析,以绘制异常基因结构,包括转录延伸过程中由RNA聚合酶(Pol)II复合物启动子近端暂停导致的DNA解链区域。尽管一直认为与DNA结合的蛋白质不能保护其下方的核酸免受KMnO4修饰,但我们在此提供证据表明,在优化条件下,这种化学物质可轻松用于检测启动子处的核因子负载。此外,通过比较体内平行的KMnO4和硫酸二甲酯(DMS)足迹分析,我们表明KMnO4与另一种化学探针结合使用可最大限度地检测DNA调控区域的因子占据情况,从而为确定活细胞中给定基因组位点处DNA-蛋白质相互作用的实际图谱提供更好的机会。