Department of Chemistry, University of Missouri, 125 Chemistry Building, Columbia, Missouri 65211, USA.
J Am Chem Soc. 2013 Jan 23;135(3):1015-25. doi: 10.1021/ja308119q. Epub 2013 Jan 11.
We recently reported that the aldehyde residue of an abasic (Ap) site in duplex DNA can generate an interstrand cross-link via reaction with a guanine residue on the opposing strand. This finding is intriguing because the highly deleterious nature of interstrand cross-links suggests that even small amounts of Ap-derived cross-links could make a significant contribution to the biological consequences stemming from the generation of Ap sites in cellular DNA. Incubation of 21-bp duplexes containing a central 5'-CAp sequence under conditions of reductive amination (NaCNBH(3), pH 5.2) generated much higher yields of cross-linked DNA than reported previously. At pH 7, in the absence of reducing agents, these Ap-containing duplexes also produced cross-linked duplexes that were readily detected on denaturing polyacrylamide gels. Cross-link formation was not highly sensitive to reaction conditions, and the cross-link, once formed, was stable to a variety of workup conditions. Results of multiple experiments including MALDI-TOF mass spectrometry, gel mobility, methoxyamine capping of the Ap aldehyde, inosine-for-guanine replacement, hydroxyl radical footprinting, and LC-MS/MS were consistent with a cross-linking mechanism involving reversible reaction of the Ap aldehyde residue with the N(2)-amino group of the opposing guanine residue in 5'-CAp sequences to generate hemiaminal, imine, or cyclic hemiaminal cross-links (7-10) that were irreversibly converted under conditions of reductive amination (NaCNBH(3)/pH 5.2) to a stable amine linkage. Further support for the importance of the exocyclic N(2)-amino group in this reaction was provided by an experiment showing that installation of a 2-aminopurine-thymine base pair at the cross-linking site produced high yields (15-30%) of a cross-linked duplex at neutral pH, in the absence of NaCNBH(3).
我们最近报道了双链 DNA 中碱基缺失(Ap)位点的醛残基可以通过与互补链上的鸟嘌呤残基反应生成链间交联。这一发现很有趣,因为链间交联的高度有害性质表明,即使是少量的 Ap 衍生交联也可能对源自细胞 DNA 中 Ap 位点产生的生物学后果产生重大贡献。在还原胺化(NaCNBH(3),pH 5.2)条件下孵育含有中央 5'-CAp 序列的 21 个碱基对的双链体,产生的交联 DNA 产率远高于以前报道的水平。在 pH 7 且没有还原剂的情况下,这些含有 Ap 的双链体也产生了易于在变性聚丙烯酰胺凝胶上检测到的交联双链体。交联形成对反应条件不是非常敏感,并且一旦形成交联,就可以在各种工作条件下稳定存在。包括 MALDI-TOF 质谱、凝胶迁移、Ap 醛的甲氧基胺封端、肌苷替代鸟嘌呤、羟基自由基足迹和 LC-MS/MS 的多项实验结果与涉及 Ap 醛残基与互补链上的 N(2)-氨基基团可逆反应的交联机制一致,在 5'-CAp 序列中生成半亚胺、亚胺或环状半亚胺交联(7-10),在还原胺化(NaCNBH(3)/pH 5.2)条件下不可逆地转化为稳定的胺键。实验表明,在交联位点安装 2-氨基嘌呤-胸腺嘧啶碱基对可在中性 pH 下(无 NaCNBH(3))产生高产率(15-30%)的交联双链体,进一步证明了该反应中外环 N(2)-氨基基团的重要性。