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三链靶向基因组交联进入可分离的缺失和碱基替换途径。

Triplex targeted genomic crosslinks enter separable deletion and base substitution pathways.

作者信息

Richards Sally, Liu Su-Ting, Majumdar Alokes, Liu Ji-Lan, Nairn Rodney S, Bernier Michel, Maher Veronica, Seidman Michael M

机构信息

Laboratory of Molecular Gerontology, National Institute on Aging, National Institutes of Health, 5600 Nathan Shock Dr, Baltimore, MD 21224, USA.

出版信息

Nucleic Acids Res. 2005 Sep 25;33(17):5382-93. doi: 10.1093/nar/gki851. Print 2005.

Abstract

We have synthesized triple helix forming oligonucleotides (TFOs) that target a psoralen (pso) interstrand crosslink to a specific chromosomal site in mammalian cells. Mutagenesis of the targeted crosslinks results in base substitutions and deletions. Identification of the gene products involved in mutation formation is important for developing practical applications of pso-TFOs, and may be informative about the metabolism of other interstrand crosslinks. We have studied mutagenesis of a pso-TFO genomic crosslink in repair proficient and deficient cells. Deficiencies in non homologous end joining and mismatch repair do not influence mutation patterns. In contrast, the frequency of base substitutions is dependent on the activity of ERCC1/XPF and polymerase zeta, but independent of other nucleotide excision repair (NER) or transcription coupled repair (TCR) genes. In NER/TCR deficient cells the frequency of deletions rises, indicating that in wild-type cells NER/TCR functions divert pso-TFO crosslinks from processes that result in deletions. We conclude that targeted pso-TFO crosslinks can enter genetically distinct mutational routes that resolve to base substitutions or deletions.

摘要

我们合成了三链螺旋形成寡核苷酸(TFOs),其靶向将补骨脂素(pso)链间交联连接到哺乳动物细胞中的特定染色体位点。靶向交联的诱变会导致碱基替换和缺失。鉴定参与突变形成的基因产物对于开发pso - TFOs的实际应用很重要,并且可能有助于了解其他链间交联的代谢情况。我们研究了在修复功能正常和缺陷的细胞中pso - TFO基因组交联的诱变情况。非同源末端连接和错配修复的缺陷不影响突变模式。相比之下,碱基替换的频率取决于ERCC1/XPF和聚合酶ζ的活性,但与其他核苷酸切除修复(NER)或转录偶联修复(TCR)基因无关。在NER/TCR缺陷细胞中,缺失的频率增加,这表明在野生型细胞中,NER/TCR功能将pso - TFO交联从导致缺失的过程中转移出来。我们得出结论,靶向的pso - TFO交联可以进入遗传上不同的突变途径,这些途径可导致碱基替换或缺失。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23f5/1236719/aadf3243eeae/gki851f1.jpg

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