未照射和紫外线照射的人成纤维细胞感染后腺病毒编码的报告基因中紫外线光产物的去除。

I P Boszko, A J Rainbow
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引用次数: 17

摘要

Ad5HCMVsp1lacZ是人巨细胞病毒即时早期启动子控制下含有lacZ基因的重组非复制型腺病毒。先前的报道表明,与来自干皮色素沉积症(XP)和Cockaye综合征(CS)患者的NER缺乏的人成纤维细胞相比,紫外线照射的Ad5HCMVsp1lacZ在核苷酸切除修复(NER)熟练患者中的lacZ表达更高,并且紫外线前治疗的正常成纤维细胞导致紫外线照射的Ad5HCMVsp1lacZ基因表达增强。我们使用了定量PCR技术来检测紫外线照射的Ad5HCMVsp1lacZ感染人成纤维细胞后,是否真的从lacZ基因中去除了紫外线光产物。将lacZ报告基因2.6 kb区域两侧的引物加入等量的Ad5HCMVsp1lacZ感染细胞提取的DNA中,并使用放射性标记核苷酸作为底物进行PCR扩增。结果显示,在正常的人成纤维细胞中,UV光产物被显著去除,但在NER缺乏的XP和CS细胞中,去除量减少,而在紫外线处理前的正常成纤维细胞中,去除量增加。
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Removal of UV photoproducts from an adenovirus-encoded reporter gene following infection of unirradiated and UV-irradiated human fibroblasts.

Ad5HCMVsp1lacZ is a recombinant nonreplicating adenovirus containing the lacZ gene under the control of the human cytomegalovirus immediate early promoter. Previous reports show that lacZ expression for UV-irradiated Ad5HCMVsp1lacZ is greater in nucleotide excision repair (NER) proficient compared to NER deficient human fibroblasts from patients with xerodermapigmentosum (XP) and Cockaye's syndrome (CS) and that pre-UV-treatment of normal fibroblasts results in an enhanced expression of the lacZ gene from UV-irradiated Ad5HCMVsp1lacZ. We have used a quantitative PCR technique to examine whether UV photoproducts are actually removed from the lacZ gene following infection of human fibroblasts with UV-irradiated Ad5HCMVsp1lacZ. Primers flanking a 2.6-kb region of the lacZ reporter gene were added to equal amounts of DNA extracted from Ad5HCMVsp1lacZ infected cells and amplified by PCR using radiolabelled nucleotides as substrates. Results show a significant removal of UV photoproducts in normal human fibroblasts, but a reduced removal in NER deficient XP and CS cells and an enhanced removal in pre-UV-treated normal fibroblasts.

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