Hanvey J C, Shimizu M, Wells R D
Department of Biochemistry, School of Medicine, University of Alabama, Birmingham 35294.
Nucleic Acids Res. 1990 Jan 11;18(1):157-61. doi: 10.1093/nar/18.1.157.
The ability of oligopyrimidines to inhibit, through triple helix formation, the specific protein-DNA interactions of the EcoRI restriction and modification enzymes (EcoRI and MEcoRI) with their recognition sequence (GAATTC) was studied. The oligonucleotides (CTT)4 and (CTT)8 formed triplexes in plasmids at (GAA)n repeats containing EcoRI sites. Cleavage and methylation of EcoRI sites within these sequences were specifically inhibited by the oligonucleotides, whereas an EcoRI site adjacent to a (GAA)n sequence was inhibited much less. Also, other EcoRI sites within the plasmid, or in exogenously added lambda DNA, were not inhibited. These results demonstrate the potential of using triplex-forming oligonucleotides to block protein-DNA interactions at specific sites, and thus this technique may be useful in chromosome mapping and in the modulation of gene expression.
研究了寡嘧啶通过形成三链螺旋抑制EcoRI限制与修饰酶(EcoRI和MEcoRI)与其识别序列(GAATTC)的特异性蛋白质-DNA相互作用的能力。寡核苷酸(CTT)4和(CTT)8在含有EcoRI位点的(GAA)n重复序列的质粒中形成三链体。这些序列内EcoRI位点的切割和甲基化被寡核苷酸特异性抑制,而与(GAA)n序列相邻的EcoRI位点受到的抑制要少得多。此外,质粒内或外源添加的λDNA中的其他EcoRI位点未受到抑制。这些结果证明了使用形成三链体的寡核苷酸在特定位点阻断蛋白质-DNA相互作用的潜力,因此该技术可能在染色体图谱绘制和基因表达调控中有用。