Bessho T, Sancar A, Thompson L H, Thelen M P
Department of Biochemistry and Biophysics, University of North Carolina School of Medicine, Chapel Hill, North Carolina 27599, USA.
J Biol Chem. 1997 Feb 7;272(6):3833-7. doi: 10.1074/jbc.272.6.3833.
The human XPF-ERCC1 protein complex is one of several factors known to be required for general nucleotide excision repair. Genetic data indicate that both proteins of this complex are necessary for the repair of interstrand cross-links, perhaps via recombination. To determine whether XPF-ERCC1 completes a set of six proteins that are sufficient to carry out excision repair, the human XPF and ERCC1 cDNAs were coexpressed in Sf21 insect cells from a baculovirus vector. The purified complex contained the anticipated 5' junction-specific endonuclease activity that is stimulated through a direct interaction between XPF and replication protein A (RPA). The recombinant complex also complemented extracts of XP-F cells and Chinese hamster ovary mutants assigned to complementation groups 1, 4, and 11. Furthermore, reconstitution of the human excision nuclease was observed with a mixture of five repair factors (XPA, XPC, XPG, TFIIH, and RPA) and the recombinant XPF-ERCC1, thus verifying that no additional protein factors are needed for the specific dual incisions characteristic of human excision repair.
人类XPF-ERCC1蛋白复合物是已知的一般核苷酸切除修复所需的几种因子之一。遗传数据表明,该复合物的两种蛋白质对于链间交联的修复都是必需的,可能是通过重组实现的。为了确定XPF-ERCC1是否构成了一组足以进行切除修复的六种蛋白质,人类XPF和ERCC1 cDNA通过杆状病毒载体在Sf21昆虫细胞中共表达。纯化的复合物具有预期的5'连接特异性内切核酸酶活性,该活性通过XPF与复制蛋白A(RPA)之间的直接相互作用而被激活。重组复合物还补充了XP-F细胞和被分配到互补组1、4和11的中国仓鼠卵巢突变体的提取物。此外,用五种修复因子(XPA、XPC、XPG、TFIIH和RPA)和重组XPF-ERCC1的混合物观察到了人类切除核酸酶的重建,从而证实了人类切除修复的特异性双切口不需要额外的蛋白质因子。