Brown P M, Fox K R
Division of Biochemistry and Molecular Biology, School of Biological Sciences, University of Southhampton, UK.
Eur J Biochem. 1999 Apr;261(1):301-10. doi: 10.1046/j.1432-1327.1999.00279.x.
We have used DNase I footprinting to examine the formation of intermolecular triplexes on DNA fragments which have been complexed with nucleosome core particles. We have prepared five DNA fragments, based on the 160-bp tyrT sequence, which contain different length oligopurine tracts (up to 25 bp) at two different positions along the fragment, and have examined their availability for triple-helix formation after reconstituting onto nucleosome core particles. These results are compared with the formation of shorter triplexes in the same regions. In general we find that increasing the length of the complex does not facilitate nucleosomal triplex formation and that the most important factor affecting triplex formation is the position of the target site within the nucleosome-bound fragment. In some instances we find that longer oligonucleotides inhibit triplex formation. Although successful triplex formation was achieved on the longest nucleosome-bound oligopurine tracts, this was accompanied by changes in cleavage pattern that suggest oligonucleotide-induced changes in nucleosome structure.
我们利用DNA酶I足迹法来检测与核小体核心颗粒复合的DNA片段上分子间三链体的形成情况。我们基于160bp的tyrT序列制备了五个DNA片段,这些片段在片段上的两个不同位置含有不同长度的寡聚嘌呤序列(最长达25bp),并在重构到核小体核心颗粒上后检测了它们形成三链体的可能性。将这些结果与相同区域中较短三链体的形成情况进行了比较。总体而言,我们发现增加复合物的长度并不会促进核小体三链体的形成,影响三链体形成的最重要因素是靶位点在与核小体结合的片段中的位置。在某些情况下,我们发现较长的寡核苷酸会抑制三链体的形成。虽然在与核小体结合的最长寡聚嘌呤序列上成功形成了三链体,但这伴随着切割模式的变化,表明寡核苷酸诱导了核小体结构的改变。