Admiraal Suzanne J, O'Brien Patrick J
Department of Biological Chemistry, University of Michigan Medical School , 1150 West Medical Center Drive, Ann Arbor, Michigan 48109-5606, United States.
Chem Res Toxicol. 2017 Jun 19;30(6):1317-1326. doi: 10.1021/acs.chemrestox.7b00057. Epub 2017 May 22.
Nicking of the DNA strand immediately upstream of an internal abasic (AP) site produces 5'-terminal abasic (dRp) DNA. Both the intact and the nicked abasic species are reactive intermediates along the DNA base excision repair (BER) pathway and can be derailed by side reactions. Aberrant accumulation of the 5'-terminal abasic intermediate has been proposed to lead to cell death, so we explored its reactivity and compared it to the reactivity of the better-characterized internal abasic intermediate. We find that the 5'-terminal abasic group cross-links with the exocyclic amine of a nucleotide on the opposing strand to form an interstrand DNA-DNA cross-link (ICL). This cross-linking reaction has the same kinetic constants and follows the same pH dependence as the corresponding cross-linking reaction of intact abasic DNA, despite the changes in charge and flexibility engendered by the nick. However, the ICL that traps nicked abasic DNA has a shorter lifetime at physiological pH than the otherwise analogous ICL of intact abasic DNA due to the reversibility of the cross-linking reaction coupled with faster breakdown of the 5'-terminal abasic species via β-elimination. Unlike internal abasic DNA, 5'-terminal abasic DNA can also react with exocyclic amines of unpaired nucleotides at the 3'-end of the nick, thereby bridging the nick by connecting DNA strands of the same orientation. The discovery and characterization of cross-links between 5'-terminal abasic sites and exocyclic amines of both opposing and adjacent nucleotides add to our knowledge of DNA damage with the potential to disrupt DNA transactions.
在内部无碱基(AP)位点上游紧邻处切割DNA链会产生5'-末端无碱基(dRp)DNA。完整的和切割后的无碱基物种都是DNA碱基切除修复(BER)途径中的反应性中间体,并且可能因副反应而偏离正常途径。有人提出5'-末端无碱基中间体的异常积累会导致细胞死亡,因此我们探究了其反应活性,并将其与特征更明确的内部无碱基中间体的反应活性进行了比较。我们发现5'-末端无碱基基团与互补链上一个核苷酸的环外胺交联,形成链间DNA-DNA交联(ICL)。尽管切割导致电荷和灵活性发生了变化,但这种交联反应具有与完整无碱基DNA相应交联反应相同的动力学常数,并且遵循相同的pH依赖性。然而,捕获切割后的无碱基DNA的ICL在生理pH下的寿命比完整无碱基DNA的类似ICL短,这是因为交联反应的可逆性以及5'-末端无碱基物种通过β-消除更快分解。与内部无碱基DNA不同,5'-末端无碱基DNA还可以与切割位点3'-末端未配对核苷酸的环外胺反应,从而通过连接相同方向的DNA链来弥合切割位点。5'-末端无碱基位点与互补及相邻核苷酸的环外胺之间交联的发现和表征,增加了我们对可能破坏DNA交易的DNA损伤的认识。