Hartman P S, Marshall A
Department of Biology, Texas Christian University, Fort Worth 76129.
Photochem Photobiol. 1992 Jan;55(1):103-11. doi: 10.1111/j.1751-1097.1992.tb04215.x.
Survival of wild-type and four radiation-sensitive (rad) mutants of the nematode Caenorhabditis elegans was determined after near-UV irradiation in the presence of 8-methoxypsoralen (8-MOP). Three sets of inactivation profiles were generated for each strain by irradiating synchronous populations of either early embryos, late embryos or first-stage larvae (L1s). Late embryos were consistently the most sensitive. Curiously, none of the four rad mutants were even moderately hypersensitive. Split-dose experiments indicated that DNA-DNA crosslinks were primarily responsible for lethality. Crosslink induction and repair were determined using two different assays. In both cases, little if any repair was observed in wild-type. This lack of repair thus explains why the rad mutants were not hypersensitive to 8-MOP photoinactivation. Since early embryos undergo extensive cell cycling, their resistance to 8-MOP photoinactivation suggests that replication is highly refractory to both monoadducts and crosslinks, as has been demonstrated previously for UV radiation-induced photoproducts (Hartman et al., 1991, Mutat. Res., 255, pp. 163-173).
在8-甲氧基补骨脂素(8-MOP)存在的情况下对线虫秀丽隐杆线虫的野生型和四种辐射敏感(rad)突变体进行近紫外辐射后,测定了它们的存活率。通过对早期胚胎、晚期胚胎或第一阶段幼虫(L1)的同步群体进行辐照,为每个菌株生成了三组失活曲线。晚期胚胎始终是最敏感的。奇怪的是,这四种rad突变体中没有一个表现出中度超敏反应。分割剂量实验表明,DNA-DNA交联是致死的主要原因。使用两种不同的测定方法确定交联诱导和修复情况。在这两种情况下,野生型中几乎没有观察到修复。因此,这种缺乏修复的情况解释了为什么rad突变体对8-MOP光灭活不超敏。由于早期胚胎经历广泛的细胞周期,它们对8-MOP光灭活的抗性表明复制对单加合物和交联都具有高度抗性,正如先前对紫外线辐射诱导的光产物所证明的那样(Hartman等人,1991年,《突变研究》,255卷,第163 - 173页)。