Sharma Kiran Kumar K, Bernhard William A
Department of Biochemistry and Biophysics, University of Rochester Medical Center, Rochester, New York 14642, USA.
J Phys Chem B. 2009 Sep 24;113(38):12839-43. doi: 10.1021/jp905750w.
Previous studies on high molecular weight DNA found that backbone damage, as monitored by free base release, is relatively independent of the type of base; i.e., the yields of all four bases were nearly equal. This could be due to a lack of influence of any given base over damage to its own deoxyribose or it could be a consequence of averaging out disparities due to each base sampling a wide range of base contexts. This study is aimed at distinguishing between these two possibilities. Transparent films, prepared from palindromic oligodeoxynucleotides of d(CTCTCGAGAG), d(CTCTCGAGAGp), d(pCTCTCGAGAGp), d(GAGAGCTCTC), d(ACGCGCGCGT), d(AACGCGCGCGTT), d(CTCTCTTAATAATTATAATTATTAAGAGAG), and d(CTCTCTTAATATTAAGAGAG), were used for this investigation. The DNA films, hydrated to approximately 2.5 waters per nucleotide, were irradiated at RT under air using X-rays generated by a tungsten tube, immediately dissolved in nuclease-free water, and stored at 277 K for 24 h, and then unaltered free base release was measured using HPLC. Yields of free base release were based on a target mass consisting of the DNA and one counterion+2.5 H2O/nucleotide. The yields of each base, G(C), G(G), G(T), and G(A) were determined for each of the above sequences. The observed yields lead to the following conclusions: (i) base release at the oligomer ends is favored over release at internal positions (called the end effect), (ii) phosphorylation of the OH moiety at the oligomer ends quenches the end effect, (iii) the magnitude of the end effect is influenced by the base at the end and the bases proximal to it, and (iv) the release of base is influenced by the base and its context.
先前对高分子量DNA的研究发现,通过游离碱基释放监测的主链损伤相对独立于碱基类型;即,所有四种碱基的产量几乎相等。这可能是由于任何给定碱基对其自身脱氧核糖损伤缺乏影响,或者这可能是由于每个碱基对广泛的碱基环境进行采样,从而平均消除差异的结果。本研究旨在区分这两种可能性。由d(CTCTCGAGAG)、d(CTCTCGAGAGp)、d(pCTCTCGAGAGp)、d(GAGAGCTCTC)、d(ACGCGCGCGT)、d(AACGCGCGCGTT)、d(CTCTCTTAATAATTATAATTATTAAGAGAG)和d(CTCTCTTAATATTAAGAGAG)的回文寡脱氧核苷酸制备的透明薄膜用于本研究。将DNA薄膜水合至每个核苷酸约2.5个水分子,在室温下于空气中使用钨管产生的X射线进行辐照,立即溶于无核酸酶水中,并在277K下储存24小时,然后使用高效液相色谱法测量未改变的游离碱基释放。游离碱基释放的产量基于由DNA和一个抗衡离子 + 2.5 H₂O/核苷酸组成的目标质量。测定了上述每个序列中每种碱基G(C)、G(G)、G(T)和G(A)的产量。观察到的产量得出以下结论:(i) 寡聚物末端的碱基释放比内部位置的释放更受青睐(称为末端效应),(ii) 寡聚物末端OH部分的磷酸化消除了末端效应,(iii) 末端效应的大小受末端碱基及其近端碱基的影响,以及(iv) 碱基的释放受碱基及其环境的影响。