Giovannangéli C, Thuong N T, Hélène C
Laboratoire de Biophysique, Muséum National d'Histoire Naturelle, INSERM U 201, CNRS UA 481, Paris, France.
Nucleic Acids Res. 1992 Aug 25;20(16):4275-81. doi: 10.1093/nar/20.16.4275.
The HIV proviral genome contains two copies of a 16 bp homopurine.homopyrimidine sequence which overlaps the recognition and cleavage site of the Dra I restriction enzyme. Psoralen was attached to the 16-mer homopyrimidine oligonucleotide, d5'(TTTTCT-TTTCCCCCCT)3', which forms a triple helix with this HIV proviral sequence. Two plasmids, containing part of the HIV proviral DNA, with either one (pLTR) or two (pBT1) copies of the 16-bp homopurine.homopyrimidine sequence and either 4 or 14 Dra I cleavage sites, respectively, were used as substrates for the psoralen-oligonucleotide conjugate. Following UV irradiation the two strands of the DNA targeted sequence were cross-linked at the triplex-duplex junction. The psoralen-oligonucleotide conjugate selectively inhibited Dra I enzymatic cleavage at sites overlapping the two triple helix-forming sequences. A secondary triplex-forming site of 8 contiguous base pairs was observed on the pBT1 plasmid when binding of the 16 base-long oligonucleotide was allowed to take place at high oligonucleotide concentrations. Replacement of a stretch of six cytosines in the 16-mer oligomer by a stretch of six guanines increased binding to the primary sites and abolished binding to the secondary site under physiological conditions. These results demonstrate that oligonucleotides can be designed to selectively recognize and modify specific sequences in HIV proviral DNA.
HIV前病毒基因组包含两个16bp的同型嘌呤-同型嘧啶序列拷贝,该序列与Dra I限制酶的识别和切割位点重叠。补骨脂素连接到16聚体同型嘧啶寡核苷酸d5'(TTTTCT-TTTCCCCCCT)3'上,该寡核苷酸与该HIV前病毒序列形成三链螺旋。两个质粒,分别含有HIV前病毒DNA的一部分,一个(pLTR)或两个(pBT1)16bp同型嘌呤-同型嘧啶序列拷贝,分别有4个或14个Dra I切割位点,用作补骨脂素-寡核苷酸缀合物的底物。紫外线照射后,DNA靶向序列的两条链在三链体-双链体连接处交联。补骨脂素-寡核苷酸缀合物在与两个形成三链螺旋的序列重叠的位点选择性抑制Dra I酶切。当在高寡核苷酸浓度下允许16个碱基长的寡核苷酸结合时,在pBT1质粒上观察到一个由8个连续碱基对组成的二级三链体形成位点。在16聚体寡聚物中用一段6个鸟嘌呤取代一段6个胞嘧啶,增加了与主要位点的结合,并在生理条件下消除了与次要位点的结合。这些结果表明,可以设计寡核苷酸来选择性识别和修饰HIV前病毒DNA中的特定序列。