Faruqi A F, Datta H J, Carroll D, Seidman M M, Glazer P M
Department of Therapeutic Radiology, Yale University School of Medicine, New Haven, Connecticut 06520-8040, USA.
Mol Cell Biol. 2000 Feb;20(3):990-1000. doi: 10.1128/MCB.20.3.990-1000.2000.
The ability to stimulate recombination in a site-specific manner in mammalian cells may provide a useful tool for gene knockout and a valuable strategy for gene therapy. We previously demonstrated that psoralen adducts targeted by triple-helix-forming oligonucleotides (TFOs) could induce recombination between tandem repeats of a supF reporter gene in a simian virus 40 vector in monkey COS cells. Based on work showing that triple helices, even in the absence of associated psoralen adducts, are able to provoke DNA repair and cause mutations, we asked whether intermolecular triplexes could stimulate recombination. Here, we report that triple-helix formation itself is capable of promoting recombination and that this effect is dependent on a functional nucleotide excision repair (NER) pathway. Transfection of COS cells carrying the dual supF vector with a purine-rich TFO, AG30, designed to bind as a third strand to a region between the two mutant supF genes yielded recombinants at a frequency of 0.37%, fivefold above background, whereas a scrambled sequence control oligomer was ineffective. In human cells deficient in the NER factor XPA, the ability of AG30 to induce recombination was eliminated, but it was restored in a corrected subline expressing the XPA cDNA. In comparison, the ability of triplex-directed psoralen cross-links to induce recombination was only partially reduced in XPA-deficient cells, suggesting that NER is not the only pathway that can metabolize targeted psoralen photoadducts into recombinagenic intermediates. Interestingly, the triplex-induced recombination was unaffected in cells deficient in DNA mismatch repair, challenging our previous model of a heteroduplex intermediate and supporting a model based on end joining. This work demonstrates that oligonucleotide-mediated triplex formation can be recombinagenic, providing the basis for a potential strategy to direct genome modification by using high-affinity DNA binding ligands.
以位点特异性方式刺激哺乳动物细胞中重组的能力,可能为基因敲除提供一种有用的工具,并为基因治疗提供一种有价值的策略。我们之前证明,三链体形成寡核苷酸(TFO)靶向的补骨脂素加合物,可在猴COS细胞的猿猴病毒40载体中诱导supF报告基因串联重复序列之间的重组。基于表明三链体即使在没有相关补骨脂素加合物的情况下也能够引发DNA修复并导致突变的研究工作,我们询问分子间三链体是否能够刺激重组。在此,我们报告三链体形成本身能够促进重组,并且这种效应依赖于功能性核苷酸切除修复(NER)途径。用富含嘌呤的TFO(AG30)转染携带双supF载体的COS细胞,AG30设计为作为第三条链结合到两个突变supF基因之间的区域,产生重组体的频率为0.37%,比背景高五倍,而随机序列对照寡聚物无效。在缺乏NER因子XPA的人类细胞中,AG30诱导重组的能力被消除,但在表达XPA cDNA的校正亚系中得以恢复。相比之下,三链体导向的补骨脂素交联诱导重组的能力在XPA缺陷细胞中仅部分降低,这表明NER不是唯一能够将靶向补骨脂素光加合物代谢为重组中间体的途径。有趣的是,在缺乏DNA错配修复的细胞中,三链体诱导的重组不受影响,这对我们之前的异源双链中间体模型提出了挑战,并支持基于末端连接的模型。这项工作表明寡核苷酸介导的三链体形成可以是重组性的,为使用高亲和力DNA结合配体指导基因组修饰的潜在策略提供了基础。