Bhattacharyya N P, Maher V M, McCormick J J
Department of Microbiology, Michigan State University, East Lansing 48824-1316.
Mutat Res. 1989 Apr;211(2):205-14. doi: 10.1016/0027-5107(89)90003-1.
To investigate the role of DNA damage in the induction of homologous recombination in mammalian cells, a series of structurally related, polycyclic aromatic carcinogens, i.e., 1-nitrosopyrene (1-NOP), N-acetoxy-2-acetylaminofluorene (N-AcO-AAF), and 4-nitroquinoline 1-oxide (4-NQO), were compared for their ability to cause intrachromosomal homologous recombination between two herpes simplex virus thymidine kinase (Htk) genes stably integrated in the genome of a tk- mouse L cell strain 333 M. Each Htk gene contains an 8-bp XhoI linker inserted at a unique site so that expression of a functional Htk enzyme requires a productive recombinational event between the two nonfunctional genes. Each carcinogen caused a dose-dependent increase in the frequency of recombination. The results were compared to what had been found previously for a structurally related carcinogen, (+/-)-7 beta, 8 alpha-dihydroxy-9 alpha, 10 alpha-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene (BPDE). As a function of concentration, BPDE was the most active agent, followed by 4-NQO, and 1-NOP, and then N-AcO-AAF. When compared on the basis of equal cell killing, the most efficient carcinogen was 1-NOP, followed by N-AcO-AAF and BPDE, and then 4-NQO. Use of tritium-labeled compounds to determine the frequency of recombination as a function of the number of adducts initially bound to DNA showed that the most effective agent was BPDE, followed by 1-NOP and 4-NQO, and then N-AcO-AAF (ratio, 6.6:2.5:1.8:1.0). To determine if these differences in recombinagenic effectiveness reflected different rates of removal of the adducts from DNA, we measured the percentage of DNA adducts removed during the 24-h period post treatment and found that 1-NOP, 4-NQO and N-AcO-AAF residues were removed at approximately the same rate, i.e., 25%-30% off. Cellular analysis of a series of independent recombinants indicated that approximately 82% of the recombinational events induced by each agent were consistent with gene conversion. DNA-DNA hybridization analysis confirmed this, and showed that each recombinant tested contained an XhoI-resistant (wild-type) Htk gene; with the majority retaining the Htk gene duplication, consistent with nonreciprocal transfer of wild-type genetic information. In the rest, only a single copy of the Htk gene remained, reflecting a single reciprocal exchange within a chromatid or a single unequal exchange between sister chromatids.
为了研究DNA损伤在哺乳动物细胞中诱导同源重组的作用,比较了一系列结构相关的多环芳烃致癌物,即1-亚硝基芘(1-NOP)、N-乙酰氧基-2-乙酰氨基芴(N-AcO-AAF)和4-硝基喹啉1-氧化物(4-NQO),它们在稳定整合于tk-小鼠L细胞系333 M基因组中的两个单纯疱疹病毒胸苷激酶(Htk)基因之间引发染色体内同源重组的能力。每个Htk基因在一个独特位点插入了一个8 bp的XhoI接头,因此功能性Htk酶的表达需要两个无功能基因之间发生有效的重组事件。每种致癌物都导致重组频率呈剂量依赖性增加。将结果与先前对结构相关致癌物(±)-7β,8α-二羟基-9α,10α-环氧-7,8,9,10-四氢苯并[a]芘(BPDE)的研究结果进行了比较。作为浓度的函数,BPDE是最活跃的试剂,其次是4-NQO和1-NOP,然后是N-AcO-AAF。在同等细胞杀伤的基础上进行比较时,最有效的致癌物是1-NOP,其次是N-AcO-AAF和BPDE,然后是4-NQO。使用氚标记化合物来确定重组频率与最初结合到DNA上的加合物数量的函数关系,结果表明最有效的试剂是BPDE,其次是1-NOP和4-NQO,然后是N-AcO-AAF(比例为6.6:2.5:1.8:1.0)。为了确定这些重组诱变效力的差异是否反映了加合物从DNA上清除的不同速率,我们测量了处理后24小时内DNA加合物清除的百分比,发现1-NOP、4-NQO和N-AcO-AAF残基以大致相同的速率被清除,即25%-30%。对一系列独立重组体的细胞分析表明,每种试剂诱导的重组事件中约82%与基因转换一致。DNA-DNA杂交分析证实了这一点,并表明每个测试的重组体都含有一个XhoI抗性(野生型)Htk基因;大多数保留了Htk基因重复,这与野生型遗传信息的非互惠转移一致。其余的重组体中,仅保留了一个Htk基因拷贝,这反映了染色体内的单次互惠交换或姐妹染色单体之间的单次不等交换。