Caputo A, Zupi G, Clanciulli A
Nucleic Acids Res. 1975 Jun;2(6):905-13. doi: 10.1093/nar/2.6.905.
By means of DNA-cellulose chromatography an enzyme with endonucleolytic activity has been isolated from nuclear acidic protein fraction of mammalian cells. The main active fraction, eluted at 0.7 M NaCl, effects the velocity sedimentation of UV-irradiated and alkylated DNA, resulting in a decrease of the molecular weight. The fraction is completely inactive using native as well as heat-denatured DNA.
通过DNA-纤维素色谱法,从哺乳动物细胞核酸性蛋白组分中分离出一种具有核酸内切酶活性的酶。主要活性组分在0.7M NaCl浓度下洗脱,它会影响紫外线照射和烷基化处理后的DNA的速度沉降,导致分子量降低。该组分对天然DNA和热变性DNA均完全无活性。