Department of Biomedical and Pharmaceutical Sciences, College of Pharmacy, University of Rhode Island, Kingston, Rhode Island 02881, USA.
Chem Res Toxicol. 2013 Jun 17;26(6):937-51. doi: 10.1021/tx400116n. Epub 2013 Jun 4.
2-Acetylaminofluorene (AAF) is a prototype arylamine carcinogen that forms C8-substituted dG-AAF and dG-AF as the major DNA lesions. The bulky N-acetylated dG-AAF lesion can induce various frameshift mutations depending on the base sequence around the lesion. We hypothesized that the thermodynamic stability of bulged-out slipped mutagenic intermediates (SMIs) is directly related to deletion mutations. The objective of the present study was to probe the structural/conformational basis of various dG-AAF-induced SMIs formed during translesion synthesis. We performed spectroscopic, thermodynamic, and molecular dynamics studies of several AAF-modified 16-mer model DNA duplexes, including fully paired and -1, -2, and -3 deletion duplexes of the 5'-CTCTCGATG[FAAF]CCATCAC-3' sequence and an additional -1 deletion duplex of the 5'-CTCTCGGCG[FAAF]CCATCAC-3' NarI sequence. Modified deletion duplexes existed in a mixture of external B and stacked S conformers, with the population of the S conformer being 'GC'-1 (73%) > 'AT'-1 (72%) > full (60%) > -2 (55%) > -3 (37%). Thermodynamic stability was in the order of -1 deletion > -2 deletion > fully paired > -3 deletion duplexes. These results indicate that the stacked S-type conformer of SMIs is thermodynamically more stable than the conformationally flexible external B conformer. Results from the molecular dynamics simulations indicate that perturbation of base stacking dominates the relative stability along with contributions from bending, duplex dynamics, and solvation effects that are important in specific cases. Taken together, these results support a hypothesis that the conformational and thermodynamic stabilities of the SMIs are critical determinants for the induction of frameshift mutations.
2-乙酰氨基芴(AAF)是一种芳基胺类致癌原,可形成 C8 取代的 dG-AAF 和 dG-AF 作为主要的 DNA 损伤。庞大的 N-乙酰化的 dG-AAF 损伤可以根据损伤周围的碱基序列诱导各种移码突变。我们假设膨出的滑动诱变中间体(SMI)的热力学稳定性与缺失突变直接相关。本研究的目的是探究在跨损伤合成过程中形成的各种 dG-AAF 诱导的 SMI 的结构/构象基础。我们对几个 AAF 修饰的 16 -mer 模型 DNA 双链体进行了光谱、热力学和分子动力学研究,包括 5'-CTCTCGATG[FAAF]CCATCAC-3'序列的完全配对和-1、-2 和-3 缺失双链体,以及 5'-CTCTCGGCG[FAAF]CCATCAC-3'NarI 序列的另一个-1 缺失双链体。修饰的缺失双链体存在于外部 B 和堆积 S 构象的混合物中,S 构象的比例为'GC'-1(73%)> 'AT'-1(72%)>完全配对(60%)> -2(55%)> -3(37%)。热力学稳定性的顺序为-1 缺失> -2 缺失>完全配对> -3 缺失双链体。这些结果表明,SMI 的堆积 S 型构象在热力学上比构象灵活的外部 B 构象更稳定。分子动力学模拟的结果表明,碱基堆积的扰动主导着相对稳定性,同时还有弯曲、双链体动力学和溶剂化效应的贡献,这些在特定情况下很重要。综上所述,这些结果支持这样一种假设,即 SMI 的构象和热力学稳定性是诱导移码突变的关键决定因素。