Yoshida S, Koiwai O, Suzuki R, Tada M
Cancer Res. 1984 May;44(5):1867-70.
In vitro modification of M13 phage single-stranded DNA with 4-hydroxyaminoquinoline 1-oxide (4HAQO) resulted in four kinds of adducts: three guanine adducts, QGI, QGII, and QGIII; and one adenine adduct, QA, at ratios of 16.4 47.3, 13.7, and 22.6, respectively. The carcinogen-modified DNA, initiated with a sequence-defined oligodeoxynucleotide primer, was replicated in vitro with Escherichia coli DNA polymerase I (Klenow fragment) and calf thymus DNA polymerases alpha and beta. The reaction products were analyzed on a DNA-sequencing gel. DNA elongation by DNA polymerase I was arrested at putative guanine adducts on the template in three ways: at one base prior to guanine; at positions opposite to guanine; and at one base beyond guanine. Similar patterns of elongation arrest were also obtained with the mammalian DNA polymerases alpha and beta. In contrast to guanine adducts, the adenine adduct, QA, might lack the capacity to arrest DNA chain elongation by DNA polymerases.
用4-羟基氨基喹啉1-氧化物(4HAQO)对M13噬菌体单链DNA进行体外修饰,产生了四种加合物:三种鸟嘌呤加合物,即QGI、QGII和QGIII;以及一种腺嘌呤加合物QA,其比例分别为16.4、47.3、13.7和22.6。用序列定义的寡脱氧核苷酸引物引发的致癌物修饰DNA,在体外由大肠杆菌DNA聚合酶I(克列诺片段)以及小牛胸腺DNA聚合酶α和β进行复制。反应产物在DNA测序凝胶上进行分析。DNA聚合酶I的DNA延伸在模板上假定的鸟嘌呤加合物处通过三种方式停止:在鸟嘌呤前一个碱基处;在与鸟嘌呤相对的位置处;以及在鸟嘌呤后一个碱基处。用哺乳动物DNA聚合酶α和β也获得了类似的延伸停止模式。与鸟嘌呤加合物不同,腺嘌呤加合物QA可能缺乏阻止DNA聚合酶进行DNA链延伸的能力。