Beger R D, Bolton P H
Department of Chemistry, Wesleyan University, Middletown, Connecticut 06459, USA.
J Biol Chem. 1998 Jun 19;273(25):15565-73. doi: 10.1074/jbc.273.25.15565.
Natural and exogenous processes can give rise to abasic sites with either a purine or pyrimidine as the base on the opposing strand. The solution state structures of the apyrimidinic DNA duplex, with D6 indicating an abasic site, [sequence: see text] referred to as AD, and the apurinic DNA duplex with a dC17, referred to as CD, have been determined. A particularly striking difference is that the abasic site in CD is predominantly a beta hemiacetal, whereas in AD the alpha and beta forms are equally present. Hydrogen bonding with water by the abasic site and the base on the opposite strand appears to play a large role in determining the structure near the damaged site. Comparison of these structures with that of a duplex DNA containing a thymine glycol at the same position as the abasic site and with that of a duplex DNA containing an abasic site in the middle of a curved DNA sequence offers some insight into the common and distinct structural features of damaged DNA sites.
自然过程和外源过程均可产生无碱基位点,其互补链上的碱基可为嘌呤或嘧啶。已确定了无嘧啶DNA双链体(其中D6表示一个无碱基位点,[序列:见原文],称为AD)和含dC17的无嘌呤DNA双链体(称为CD)的溶液状态结构。一个特别显著的差异是,CD中的无碱基位点主要是β-半缩醛形式,而在AD中,α-和β-形式等量存在。无碱基位点与互补链上碱基与水之间的氢键作用似乎在决定损伤位点附近的结构方面起着重要作用。将这些结构与在与无碱基位点相同位置含有胸腺嘧啶乙二醇的双链DNA结构以及在弯曲DNA序列中间含有无碱基位点的双链DNA结构进行比较,有助于深入了解受损DNA位点的共同和独特结构特征。