Kunkel T A, Sabatino R D, Bambara R A
Proc Natl Acad Sci U S A. 1987 Jul;84(14):4865-9. doi: 10.1073/pnas.84.14.4865.
The fidelity of DNA synthesis by calf thymus DNA polymerase delta (pol delta) in vitro has been determined using an M13lacZ alpha nonsense codon reversion assay. Pol delta is highly accurate, producing on average less than 1 single-base substitution error for each 10(6) nucleotides polymerized. This accuracy is 10- and 500-fold greater than that of DNA polymerases alpha and beta, respectively, in the same assay. Three observations suggest that this higher fidelity results in part from proofreading of misinserted bases by the 3' to 5' exonuclease associated with pol delta. First, the exonuclease efficiently excises terminally mismatched bases. Second, both terminal mismatch excision and the fidelity of DNA synthesis by pol delta are reduced with increasing concentration of deoxynucleoside triphosphates in the synthesis reaction. These effects result from increasing the rate of polymerization relative to the rate of exonucleolytic excision and are hallmarks of exonuclease proofreading. Third, both terminal mismatch excision and fidelity decrease upon addition to the reaction mixture of adenosine monophosphate, a compound known to selectively inhibit the exonuclease but not the polymerase activity of pol delta. These results suggest that 3' to 5' exonuclease-dependent proofreading enhances the fidelity of DNA synthesis by a mammalian DNA polymerase in vitro.
利用M13lacZα无义密码子回复分析,已测定了小牛胸腺DNA聚合酶δ(pol δ)在体外进行DNA合成时的保真度。Pol δ高度准确,在每聚合10⁶个核苷酸时平均产生少于1个单碱基替换错误。在相同分析中,这种准确性分别比DNA聚合酶α和β高10倍和500倍。三项观察结果表明,这种更高的保真度部分源于与pol δ相关的3'至5'外切核酸酶对错配插入碱基的校正。首先,外切核酸酶能有效切除末端错配碱基。其次,随着合成反应中脱氧核苷三磷酸浓度的增加,pol δ的末端错配切除和DNA合成保真度均降低。这些效应是由于聚合速率相对于外切核酸酶切除速率增加所致,是外切核酸酶校正的特征。第三,在反应混合物中加入已知能选择性抑制pol δ外切核酸酶活性而非聚合酶活性的单磷酸腺苷后,末端错配切除和保真度均降低。这些结果表明,3'至5'外切核酸酶依赖性校正增强了哺乳动物DNA聚合酶在体外进行DNA合成时的保真度。