Lambert M W, Fenkart D, Clarke M
Department of Pathology, UMDNJ-New Jersey Medical School, Newark 07103.
Mutat Res. 1988 Jan;193(1):65-73. doi: 10.1016/0167-8817(88)90008-9.
DNA endonuclease activities from the chromatin of normal human and xeroderma pigmentosum, complementation group A (XPA), lymphoblastoid cells were examined on DNA treated with 8-methoxypsoralen (8-MOP) or 4,5',8-trimethylpsoralen (TMP) plus long wavelength ultraviolet (UVA) light, which produce monoadducts and DNA interstrand cross-links, and angelicin plus UVA light, which produces mainly monoadducts. 9 chromatin-associated DNA endonuclease activities were isolated from normal and XPA cells and assayed for activity on PM2 bacteriophage DNA that had been treated with 8-MOP or TMP in the dark and then exposed to UVA light. Unbound psoralen was removed by dialysis and a second dose of UVA light was given. Cross-linking of DNA molecules was confirmed by alkaline gel electrophoresis. In both normal and XPA cells, two DNA endonuclease activities were found which were active on 8-MOP and TMP plus UVA light treated DNA. One of these endonuclease activities, pI 4.6, is also active on intercalated DNA and a second one, pI 7.6, is also active on UVC (254 nm) light irradiated DNA. The major activity against angelicin plus UVA light treated DNA in both normal and XPA cells was found in the fraction, pI 7.6. The levels of activity of both of these fractions on all 3 psoralen-damaged DNAs were similar between normal and XPA cells. These results indicate that in both normal and XPA cells there are at least two different DNA endonucleases which act on both 8-MOP and TMP plus UVA light treated DNA.
对正常人及着色性干皮病A组(XPA)淋巴母细胞染色质中的DNA内切酶活性进行了检测,检测对象为经8-甲氧基补骨脂素(8-MOP)或4,5',8-三甲基补骨脂素(TMP)加长波紫外线(UVA)照射处理的DNA,这两种处理会产生单加合物和DNA链间交联,以及经当归素加UVA照射处理的DNA,这种处理主要产生单加合物。从正常细胞和XPA细胞中分离出9种与染色质相关的DNA内切酶活性,并检测其对在黑暗中用8-MOP或TMP处理后再暴露于UVA光的PM2噬菌体DNA的活性。通过透析去除未结合的补骨脂素,并给予第二剂UVA光。通过碱性凝胶电泳确认DNA分子的交联。在正常细胞和XPA细胞中,均发现两种对8-MOP和TMP加UVA光处理的DNA有活性的DNA内切酶活性。其中一种内切酶活性,pI为4.6,对插入的DNA也有活性,另一种,pI为7.6,对紫外线C(254nm)照射的DNA也有活性。在正常细胞和XPA细胞中,针对当归素加UVA光处理的DNA的主要活性存在于pI为7.6的组分中。正常细胞和XPA细胞中这两种组分对所有3种补骨脂素损伤的DNA的活性水平相似。这些结果表明,在正常细胞和XPA细胞中,至少有两种不同的DNA内切酶作用于8-MOP和TMP加UVA光处理的DNA。