Tornaletti S, Pfeifer G P
Department of Biology, Beckman Research Institute of the City of Hope, Duarte, CA 91010, USA.
Bioessays. 1996 Mar;18(3):221-8. doi: 10.1002/bies.950180309.
The formation of DNA photoproducts by ultraviolet (UV) light is responsible for induction of mutations and development of skin cancer. To understand UV mutagenesis, it is important to know the mechanisms of formation and repair of these lesions. Cyclobutane pyrimidine dimers and (6-4)photoproducts are the two major classes of UV-induced DNA lesions. Their distribution along DNA sequences in vivo is strongly influenced by nucleosomes and other DNA binding proteins. Repair of UV photoproducts is dependent on the transcriptional status of the sequences to be repaired and on the chromatin environment. Sensitive techniques are now available to study repair of UV damage at the level of nucleotide resolution in mammalian cells. With the aid of in vitro systems, the entire nucleotide excision repair process has been reconstituted from purified protein components with naked DNA as a substrate. Future work will focus on the development of in vitro assays for transcription-coupled repair and repair in chromatin.
紫外线(UV)诱导的DNA光产物的形成是导致突变和皮肤癌发生的原因。为了理解UV诱变作用,了解这些损伤的形成和修复机制很重要。环丁烷嘧啶二聚体和(6-4)光产物是UV诱导的两类主要DNA损伤。它们在体内沿DNA序列的分布受到核小体和其他DNA结合蛋白的强烈影响。UV光产物的修复取决于待修复序列的转录状态和染色质环境。现在已有灵敏的技术可用于在哺乳动物细胞中以核苷酸分辨率水平研究UV损伤的修复。借助体外系统,已经以裸DNA为底物,从纯化的蛋白质成分中重建了整个核苷酸切除修复过程。未来的工作将集中于开发用于转录偶联修复和染色质修复的体外检测方法。