Zöllner E J, Störger H, Breter H J, Zahn R K
Z Naturforsch C Biosci. 1975 Nov-Dec;30(6):781-4. doi: 10.1515/znc-1975-11-1215.
Four groups of deoxyribonuclease activities from human lymphocytes have been characterized by deoxyribonuclease assay in DNA-containing polyacrylamide gels following their separation by disc-electrophoresis. All activities hydrolyse DNA endonucleolytically. One neutral deoxyribonuclease found in the cytoplasmic fraction prefers native or UV-irradiated DNA over denatured DNA as substrate and is a 5'-monoester former. Two groups of acid deoxyribonuclease activities are detectable in the nuclear fraction. Both are 3'-monoester formers. One is as well active with denatured DNA as with native DNA, the other one shows the same activity with native and UV-irradiated DNA but lower activity with denatured DNA. An alkaline deoxyribonuclease activity, also localized in the nucleus, is a 5'-monoester former, and prefers denatured or UV-irradiated DNA as substrate.
通过盘状电泳分离后,在含DNA的聚丙烯酰胺凝胶中进行脱氧核糖核酸酶测定,已对来自人淋巴细胞的四组脱氧核糖核酸酶活性进行了表征。所有活性均以内切核酸酶的方式水解DNA。在细胞质部分发现的一种中性脱氧核糖核酸酶,与变性DNA相比,更倾向于将天然或紫外线照射的DNA作为底物,并且是一种5'-单酯形成酶。在细胞核部分可检测到两组酸性脱氧核糖核酸酶活性。两者都是3'-单酯形成酶。一种对变性DNA和天然DNA的活性相同,另一种对天然和紫外线照射的DNA具有相同活性,但对变性DNA的活性较低。一种也定位于细胞核的碱性脱氧核糖核酸酶活性是一种5'-单酯形成酶,并且更倾向于将变性或紫外线照射的DNA作为底物。