Thoma Brian S, Vasquez Karen M
Department of Carcinogenesis, The University of Texas M. D. Anderson Cancer Center, Science Park-Research Division, Smithville, Texas, USA.
Mol Carcinog. 2003 Sep;38(1):1-13. doi: 10.1002/mc.10143.
It has been reported that 80-90% of human cancers may result, in part, from DNA damage. Cell survival depends critically on the stability of our DNA and exquisitely sensitive DNA repair mechanisms have developed as a result. In humans, nucleotide excision repair (NER) protects the DNA against the mutagenic effects of carcinogens and ultraviolet (UV) radiation from sun exposure. By preventing mutations from forming in the DNA, the repair machinery ultimately protects us from developing cancers. DNA damage recognition is the rate-limiting step in repair, and although many details of NER have been elucidated, the mechanisms by which DNA damage is recognized remain to be fully determined. Two primary protein complexes have been proposed as the damaged DNA recognition factor in NER: xeroderma pigmentosum protein A-replication protein A (XPA-RPA) and xeroderma pigmentosum protein C-human homolog of RAD23B (XPC-hHR23B). Here we compare the evidence that supports damage detection by these protein complexes and propose a model for DNA damage recognition in NER based on the current understanding of the roles these proteins may play in the processing of DNA lesions.
据报道,80% - 90%的人类癌症可能部分源于DNA损伤。细胞的存活严重依赖于我们DNA的稳定性,因此进化出了极其敏感的DNA修复机制。在人类中,核苷酸切除修复(NER)可保护DNA免受致癌物和阳光中紫外线(UV)辐射的诱变作用。通过防止DNA中形成突变,修复机制最终保护我们免受癌症的侵害。DNA损伤识别是修复过程中的限速步骤,尽管NER的许多细节已得到阐明,但DNA损伤的识别机制仍有待完全确定。两种主要的蛋白质复合物被认为是NER中受损DNA的识别因子:着色性干皮病蛋白A - 复制蛋白A(XPA - RPA)和着色性干皮病蛋白C - RAD23B的人类同源物(XPC - hHR23B)。在此,我们比较支持这些蛋白质复合物进行损伤检测的证据,并基于目前对这些蛋白质在DNA损伤处理中可能发挥的作用的理解,提出一种NER中DNA损伤识别的模型。