Rahn R O
Nucleic Acids Res. 1976 Apr;3(4):879-90. doi: 10.1093/nar/3.4.879.
Poly(d[14C]A), p(dA)2, and [14C]adenosine-labeled DNA were irradiated at 254 nm with fluences up to 50 J/m2, and then following formic acid hydrolysis at 170 degrees C WERE SUBJECTED TO PAPER CHROMAtography using a butanol:water:acetic acid (80:30:12) solvent system. For poly(dA), up to 25% of the radioactivity appeared as fluorescent material located in the Rf 0.21-0.29 region. The hydrolysate of the purified photoproduct, p(dA)2, isolated from irradiated p(dA)2 by DEAE chromatography also had an Rf of 0.29 as well as an absorbance maximum at 310 nm. In all cases studied, however, the photoproduct yield in the Rf 0.29 region for native DNA was less than 2%. Denaturation of the DNA appeared to enhance the yield slightly, although no pronounced peak in this region of the chromatogram was discerned. Mechanistic studies indicate that the yield of the adenine photoproduct in poly(dA) is favored by base stacking, has a singlet excimer as a precursor, and is quenched by hydrogen bonding to a pyrimidine. It is concluded that the yield of the adenine photoproduct in both native and denatured DNA is considerably less than in poly (dA) and in all probability does not represent a biologically significant product.
用高达50 J/m²的辐照量在254 nm波长下对聚(d[¹⁴C]A)、p(dA)₂和[¹⁴C]腺苷标记的DNA进行辐照,然后在170℃进行甲酸水解,之后使用丁醇:水:乙酸(80:30:12)溶剂系统进行纸色谱分析。对于聚(dA),高达25%的放射性表现为位于比移值0.21 - 0.29区域的荧光物质。通过DEAE色谱从辐照后的p(dA)₂中分离出的纯化光产物p(dA)₂的水解产物,其比移值也为0.29,且在310 nm处有最大吸光度。然而,在所有研究的情况下,天然DNA在比移值0.29区域的光产物产率均低于2%。DNA的变性似乎略微提高了产率,尽管在色谱图的该区域未观察到明显的峰。机理研究表明,聚(dA)中腺嘌呤光产物的产率受碱基堆积的促进,以单线态激基缔合物作为前体,并通过与嘧啶形成氢键而猝灭。得出的结论是,天然和变性DNA中腺嘌呤光产物的产率均远低于聚(dA),而且很可能不代表具有生物学意义的产物。