紫外线辐射诱导的角膜DNA中嘧啶二聚体的光修复

Ronald D. Ley, Lee A. Applegate, Steven F. Freeman
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引用次数: 16

摘要

利用黄体微球菌损伤特异性核酸酶结合琼脂糖凝胶电泳技术,在紫外照射的有袋动物家蝇角膜上皮中测定了DNA中嘧啶二聚体的诱导和光修复。我们观察到FS-40太阳灯(280-400 nm)每J/m2每千碱基(kb) DNA诱导7.2±1.0 × 10−5个嘧啶二聚体。在100 J/m2之后,50%和>90%的二聚体分别在10分钟和30分钟的光活化光(320-400 nm)下进行光修复。此外,300 J/m2和500 J/m2诱导的二聚体中,分别有70%和60%的二聚体在光活化光下暴露60分钟后得到修复。家蝇角膜上皮光修复嘧啶二聚体的能力使其成为确定嘧啶二聚体是否参与辐照眼睛病理变化的潜在有用模型。
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Photorepair of ultraviolet radiation-induced pyrimidine dimers in corneal DNA

The induction and photorepair of pyrimidine dimers in DNA have been measured in the ultraviolet-irradiated, corneal epithelium of the marsupial, Monodelphis domestica, using damage-specific nucleases from Micrococcus luteus in conjunction with agarose gel electrophoresis. We observed that FS-40 sunlamps (280–400 nm) induced 7.2 ± 1.0 × 10−5 pyrimidine dimers per kilobase (kb) of DNA per J/m2. Following 100 J/m2, 50% and > 90% of the dimers were photorepaired during a 10- and 30-min exposure to photoreactivating light (320–400 nm), respectively. In addition ∼ 70% and ∼ 60% of the dimers induced by 300 and 500 J/m2, respectively, were repaired by a 60-min exposure to photoreactivating light. The capacity of the corneal epithelium of M. domestica to photorepair pyrimidine dimers identifies this animal as a potentially useful model withwhich to determine whether pyrimidine dimers are involved in pathological changes of the irradiated eye.

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