Guillonneau F, Guieysse A L, Nocentini S, Giovannangeli C, Praseuth D
Laboratoire de Biophysique, INSERM U565, CNRS UMR5153, Muséum National d'Histoire Naturelle, 43 rue Cuvier, 75231 Paris Cedex 05, France.
Nucleic Acids Res. 2004 Feb 13;32(3):1143-53. doi: 10.1093/nar/gkh267. Print 2004.
Targeting DNA-damaging agents to specific DNA sites by using sequence-specific DNA ligands has been successful in directing genomic modifications. The understanding of repair processing of such targeted damage and the influence of the adjacent complex is largely unknown. In this way, directed interstrand cross-links (ICLs) have already been generated by psoralen targeting. The mechanisms responsible for ICL removal are far from being understood in mammalian cells, with the proposed involvement of both mutagenic and recombinogenic pathways. Here, a unique ICL was introduced at a selected site by photoactivation of a psoralen moiety with the use of psoralen conjugates of triplex-forming oligonucleotides. The processing of psoralen ICL was evaluated in vitro and in cells for two types of cross-linked substrates, either containing a psoralen ICL alone or with an adjacent triple-stranded structure. We show that the presence of a neighbouring triplex structure interferes with different stages of psoralen ICL processing: (i) the ICL-induced DNA repair synthesis in HeLa cell extracts is inhibited by the triplex structure, as measured by the efficiency of 'true' and futile repair synthesis, stopping at the ICL site; (ii) in HeLa cells, the ICL removal via a nucleotide excision repair (NER) pathway is delayed in the presence of a neighbouring triplex; and (iii) the binding to ICL of recombinant xeroderma pigmentosum A protein, which is involved in pre-incision recruitment of NER factors is impaired by the presence of the third DNA strand. These data characterize triplex-induced modulation of ICL repair pathways at specific steps, which might have implications for the controlled induction of targeted genomic modifications and for the associated cellular responses.
通过使用序列特异性DNA配体将DNA损伤剂靶向特定DNA位点已成功用于指导基因组修饰。对于这种靶向损伤的修复过程以及相邻复合物的影响,人们了解得还很少。通过补骨脂素靶向已经产生了定向链间交联(ICL)。在哺乳动物细胞中,负责ICL去除的机制远未被理解,有人提出诱变和重组途径都参与其中。在这里,通过使用三链形成寡核苷酸的补骨脂素缀合物对补骨脂素部分进行光活化,在选定的位点引入了独特的ICL。针对两种类型的交联底物,即单独含有补骨脂素ICL或带有相邻三链结构的底物,在体外和细胞中评估了补骨脂素ICL的处理情况。我们表明,相邻三链结构的存在会干扰补骨脂素ICL处理的不同阶段:(i)如通过“真正”和无效修复合成的效率所测量的,三链结构会抑制HeLa细胞提取物中ICL诱导的DNA修复合成,在ICL位点处停止;(ii)在HeLa细胞中,存在相邻三链时,通过核苷酸切除修复(NER)途径的ICL去除会延迟;(iii)第三条DNA链的存在会损害参与NER因子切口前募集的重组着色性干皮病A蛋白与ICL的结合。这些数据表征了三链在特定步骤对ICL修复途径的诱导调节,这可能对靶向基因组修饰的可控诱导以及相关的细胞反应具有影响。