Jain Nidhi, Li Yuyuan, Zhang Li, Meneni Srinivasa R, Cho Bongsup P
Department of Biomedical and Pharmaceutical Sciences, College of Pharmacy, University of Rhode Island, Kingston, Rhode Island 02881, USA.
Biochemistry. 2007 Nov 20;46(46):13310-21. doi: 10.1021/bi701386f. Epub 2007 Oct 26.
The NarI recognition sequence (5'-G1G2CG3CN-3') is the most vulnerable hot spot for frameshift mutagenesis induced by the carcinogen 2-aminofluorene and its analogues in Escherichia coli. Lesioning of the guanine in the G3 position induces an especially high frequency of -2 deletion mutations; vulnerability to these mutations is modulated by the nature of the nucleotide in the N position (C approximately A > G > T). The objective of the present study was to probe the structural basis of this N-mediated influence on the propensity of the G3 lesion to form a slipped mutagenic intermediate (SMI) during translesion synthesis. We studied NarI-based fully paired [(5'-CTCG1G2CG3CNATC-3')(5'-GATNCGGCCGAG-3'), N = dC or dT] and -2 deletion [(5'-CTCG1G2CG3CNATC-3')(5'-GATNGCCGAG-3'), N = dC or dT] duplexes, in which G* was either AF [N-(2'-deoxyguanosin-8-yl)-2-aminofluorene] or the 19F probe FAF [N-(2'-deoxyguanosin-8-yl)-7-fluoro-2-aminofluorene]. The latter sequences mimic the bulged SMI for -2 deletion mutations. Dynamic 19F NMR, circular dichroism, and UV melting results indicated that the NarI-dC/-2 deletion duplex adopts exclusively an intercalated conformer, whereas the NarI-dT/-2 deletion duplex exists as multiple conformers. The data support the presence of a putative equilibrium between a carcinogen-intercalated and a carcinogen-exposed SMI for the dT/-2 duplex. A similar dT-induced conformational heterogeneity was observed for the fully paired duplexes in which all three guanines were individually modified by AF or FAF. The frequency of the carcinogen stacked S-conformation was found to be highest (69-75%) at the G3 hot spot in NarI-dC duplexes. Taken together, our results support the hypothesis that the conformational stability of the SMI is a critical determinant for the efficacy of -2 frameshift mutagenesis in the NarI sequence. We also provide evidence for AF/FAF conformational compatibility in the NarI sequences.
NarI识别序列(5'-G1G2CG3CN-3')是致癌物2-氨基芴及其类似物在大肠杆菌中诱导移码突变的最脆弱热点。G3位置的鸟嘌呤损伤诱导-2缺失突变的频率特别高;对这些突变的易感性受N位置核苷酸性质的调节(C≈A>G>T)。本研究的目的是探究这种N介导的对G3损伤在跨损伤合成过程中形成滑动诱变中间体(SMI)倾向的影响的结构基础。我们研究了基于NarI的完全配对双链体[(5'-CTCG1G2CG3CNATC-3')(5'-GATNCGGCCGAG-3'),N = dC或dT]和-2缺失双链体[(5'-CTCG1G2CG3CNATC-3')(5'-GATNGCCGAG-3'),N = dC或dT],其中G*要么是AF [N-(2'-脱氧鸟苷-8-基)-2-氨基芴],要么是19F探针FAF [N-(2'-脱氧鸟苷-8-基)-7-氟-2-氨基芴]。后一种序列模拟了-2缺失突变的凸起SMI。动态19F NMR、圆二色性和紫外熔解结果表明,NarI-dC/-2缺失双链体仅采用插入构象,而NarI-dT/-2缺失双链体以多种构象存在。数据支持dT/-2双链体在致癌物插入的SMI和致癌物暴露的SMI之间存在假定平衡。对于所有三个鸟嘌呤分别用AF或FAF修饰的完全配对双链体,也观察到了类似的dT诱导的构象异质性。发现在NarI-dC双链体的G3热点处,致癌物堆积的S构象频率最高(69-75%)。综上所述,我们的结果支持以下假设:SMI的构象稳定性是NarI序列中-2移码诱变效率的关键决定因素。我们还提供了NarI序列中AF/FAF构象兼容性的证据。