Guyer R B, Deering R A
Biochim Biophys Acta. 1985 Apr 19;824(4):304-12. doi: 10.1016/0167-4781(85)90036-3.
Two apurinic/apyrimidinic- (AP-) specific endonuclease activities have been isolated from the cells of Dictyostelium discoideum by fractionation on DEAE-cellulose, CM-cellulose and Sephadex G-75. These activities, designated A and B, have apparent molecular weights of 49000 and 40000, respectively. Although their precise reaction optima differ somewhat, both A and B quantitatively nick AP DNA best at pH 8.0-8.5 in low salt (less than 100 mM NaCl); both require Mg2+. These activities are apparently specific only for AP sites in DNA. The low activities observed on heavily ultraviolet-irradiated DNA, gamma-irradiated DNA and osmium tetroxide-treated DNA are consistent with the small numbers of secondary AP sites expected in these DNAs. Both A and B produce single-strand nicks in AP DNA that result in termini that serve as good primers for Escherichia coli polymerase I. Hence, A and B appear to be Class II AP endonucleases which yield 3'-OH termini at nicks on the 5' side of baseless sugars. It is unclear whether A and B are independently coded proteins, different post-translational modifications of the same gene product, or whether one is an artifact arising from the isolation. Many of the properties of these D. discoideum AP endonuclease activities are similar to those of the predominant AP endonucleases observed in bacterial, plant and animal cells. They will be of use in the characterization of excision repair in this organism.
通过在DEAE - 纤维素、CM - 纤维素和葡聚糖凝胶G - 75上进行分级分离,从盘基网柄菌细胞中分离出了两种脱嘌呤/脱嘧啶(AP)特异性内切核酸酶活性。这些活性分别命名为A和B,其表观分子量分别为49000和40000。尽管它们精确的反应最适条件略有不同,但A和B在低盐(小于100 mM NaCl)条件下,于pH 8.0 - 8.5时对AP DNA进行定量切口的效果最佳;二者都需要Mg2 +。这些活性显然仅对DNA中的AP位点具有特异性。在重度紫外线照射的DNA、γ射线照射的DNA和四氧化锇处理的DNA上观察到的低活性,与这些DNA中预期的少量二级AP位点一致。A和B都在AP DNA中产生单链切口,这些切口产生的末端可作为大肠杆菌聚合酶I的良好引物。因此,A和B似乎是II类AP内切核酸酶,它们在无碱基糖5'侧的切口处产生3'-OH末端。目前尚不清楚A和B是独立编码的蛋白质、同一基因产物的不同翻译后修饰,还是其中一个是分离过程中产生的假象。这些盘基网柄菌AP内切核酸酶活性的许多特性与在细菌、植物和动物细胞中观察到的主要AP内切核酸酶的特性相似。它们将有助于对该生物体中的切除修复进行表征。