Sugasawa K, Masutani C, Hanaoka F
Cellular Physiology Laboratory, Institute of Physical and Chemical Research (RIKEN), Saitama, Japan.
J Biol Chem. 1993 Apr 25;268(12):9098-104.
Simian virus 40 minichromosomes were irradiated with ultraviolet light and used to study cell-free DNA repair reactions by soluble extracts of repair-proficient human cells. Damage-specific incorporation of labeled nucleotides was measured after linearization and electrophoresis of the viral DNA. Repair synthesis with irradiated chromosomes was dependent on the dose of ultraviolet light, but naked viral DNA irradiated at the same doses showed significantly higher template activity. The reactions absolutely required the presence of cell extract, but an extract from Chinese hamster cells was as active as those from human cells. The repair activity was apparently stimulated by the addition of unirradiated plasmid DNA, which did not affect the nucleosome density of the viral chromosomes. ATP and its regenerating system were required for the reaction, but total repair synthesis was little affected by exogenous addition of substrates for RNA synthesis and poly(ADP-ribosyl)ation. Most of the repaired viral chromosomal DNA was in the supercoiled, closed circular form, suggesting that excision repair reactions proceeded to the stage of ligation in the present cell-free system.
用紫外线照射猿猴病毒40微小染色体,并用于通过修复能力强的人类细胞的可溶性提取物研究无细胞DNA修复反应。在病毒DNA线性化和电泳后,测量标记核苷酸的损伤特异性掺入。用照射过的染色体进行修复合成取决于紫外线剂量,但相同剂量照射的裸露病毒DNA显示出明显更高的模板活性。这些反应绝对需要细胞提取物的存在,但中国仓鼠细胞的提取物与人类细胞的提取物活性相同。通过添加未照射的质粒DNA明显刺激了修复活性,这并不影响病毒染色体的核小体密度。反应需要ATP及其再生系统,但外源添加RNA合成和聚(ADP-核糖基)化的底物对总修复合成影响很小。大多数修复的病毒染色体DNA呈超螺旋、闭环形式,这表明在目前的无细胞系统中,切除修复反应进行到了连接阶段。