Gruenert D C, Cleaver J E
Cancer Res. 1985 Nov;45(11 Pt 1):5399-404.
SV40-transformed normal, xeroderma pigmentosum (XP) and Fanconi's anemia (FA) fibroblasts have distinct repair capacities for monoadducts and DNA interstrand cross-links produced by exposure to near-UV (320-400 nm) light in the presence of 8-methoxypsoralen or angelicin. Excision repair of monoadducts occurred rapidly in normal and FA cells after exposure but not in XP cells. Cross-links were repaired in normal cells with a t1/2 of about 10 h but not in XP or FA cells. When the total number of adducts induced by 8-methoxypsoralen in normal cells was kept constant, the amount of repair replication decreased as the ratio of cross-links to monoadducts increased. This suggests either that cross-link repair is significantly different from monoadduct repair, involving smaller patches and a much slower rate of patching or that cross-links can inhibit monoadduct repair. Our results show that XP group A and FAH12 cell lines are deficient in cross-link repair. The data also suggest that the mechanism of cross-link repair in human cells involves several enzymes and that different ones may be deficient in XP and FA cells.
SV40转化的正常细胞、着色性干皮病(XP)细胞和范科尼贫血(FA)成纤维细胞,对于在8-甲氧基补骨脂素或白芷香豆素存在的情况下,暴露于近紫外线(320 - 400纳米)光所产生的单加合物和DNA链间交联,具有不同的修复能力。暴露后,正常细胞和FA细胞中单加合物的切除修复迅速发生,但XP细胞中则不然。正常细胞中交联在约10小时的t1/2时间内得到修复,但XP细胞或FA细胞中则没有。当正常细胞中8-甲氧基补骨脂素诱导的加合物总数保持恒定时,随着交联与单加合物比例的增加,修复复制量减少。这表明要么交联修复与单加合物修复显著不同,涉及更小的片段和更慢的修补速率,要么交联可以抑制单加合物修复。我们的结果表明,XP A组和FAH12细胞系在交联修复方面存在缺陷。数据还表明,人类细胞中交联修复的机制涉及多种酶,并且不同的酶在XP细胞和FA细胞中可能存在缺陷。