Two DNA endonuclease activities from normal human and xeroderma pigmentosum chromatin active on psoralen plus ultraviolet light treated DNA

Muriel W. Lambert, Douglas Fenkart, Mark Clarke
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引用次数: 21

Abstract

DNA endonuclease activities from the chromatin of normal human and xeroderma pigmentosum, complementing group A (XPA), lymphoblastoid cells were examined on DNA treated with 8-methoxy-psoralen (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.

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两种DNA内切酶活性来自正常人和色素干皮病的染色质上的补骨脂素加紫外光处理的DNA
用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)光处理的DNA,以及angelicin加UVA光处理的DNA,检测了正常人和A互补组(XPA)、淋巴母细胞样细胞染色质DNA内切酶活性。从正常细胞和XPA细胞中分离出9个染色质相关DNA内切酶活性,并测定了在黑暗中用8-MOP或TMP处理后暴露在UVA光下的PM2噬菌体DNA上的活性。通过透析去除未结合的补骨脂素,并给予第二剂量的UVA光。碱性凝胶电泳证实了DNA分子的交联。在正常细胞和XPA细胞中,发现两种DNA内切酶活性分别活跃于8-MOP和TMP + UVA光处理的DNA上。其中一个内切酶pI 4.6在插入DNA上也有活性,另一个pI 7.6在UVC (254 nm)光照射的DNA上也有活性。在正常细胞和XPA细胞中,对angelicin + UVA光处理的DNA的主要活性在pI 7.6中被发现。这两种组分对所有3种补骨脂素损伤dna的活性水平在正常细胞和XPA细胞之间是相似的。这些结果表明,在正常和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。
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