Kunkel T A, Loeb L A, Goodman M F
J Biol Chem. 1984 Feb 10;259(3):1539-45.
The fidelity with which wild type T4 DNA polymerase copies phi X174 amber 3 plus strand DNA at position 587 in vitro has been measured. Synthesis is initiated by hybridizing to the template a HaeIII restriction fragment whose 3'-OH terminus is 83 nucleotides from the amber 3 site. Based on gel electrophoresis of product DNA molecules and genetic marker rescue data, T4 DNA polymerase copies significantly beyond the mutant site. Transfection analysis shows that the A X T leads to G X C mutation at position 587 occurs 10- to 100-fold less frequently with T4 DNA polymerase than with E. coli DNA polymerase I. The aberrant incorporation of cytosine opposite adenine at position 587 by the T4 polymerase alone is occurring at a frequency not greater than about 10(-7) which, for this particular locus, may be similar to the fidelity exhibited by the T4 accessory proteins plus the polymerase comprising the replication complex. A comparison of the accuracy of mutator L56 and antimutator L141 T4 DNA polymerases relative to wild type shows at most a 2- to 4-fold decrease and increase, respectively, in fidelity. When compared to 10- to 1000-fold effects on mutation frequencies that these same mutant alleles have in vivo, these results suggest that the wide range in expression of mutator and antimutator phenotypes in vivo may be dependent on an abnormal interaction of the aberrant DNA polymerases with other protein components of the replication complex.
已测定野生型T4 DNA聚合酶在体外复制φX174琥珀3正链DNA第587位时的保真度。通过将一个HaeIII限制性片段与模板杂交来起始合成,该片段的3'-OH末端距琥珀3位点83个核苷酸。基于产物DNA分子的凝胶电泳和遗传标记拯救数据,T4 DNA聚合酶的复制显著超过突变位点。转染分析表明,与大肠杆菌DNA聚合酶I相比,T4 DNA聚合酶导致第587位A×T到G×C突变的频率低10到100倍。仅T4聚合酶在第�87位腺嘌呤对面错误掺入胞嘧啶的频率不大于约10^(-7),对于这个特定位点,这可能与T4辅助蛋白加上组成复制复合物的聚合酶所表现出的保真度相似。将突变型L56和抗突变型L141 T4 DNA聚合酶相对于野生型的准确性进行比较,结果表明保真度最多分别降低2至4倍和提高2至⁴倍。与这些相同突变等位基因在体内对突变频率产生的10至1000倍的影响相比,这些结果表明体内突变型和抗突变型表型表达的广泛差异可能取决于异常DNA聚合酶与复制复合物其他蛋白质成分的异常相互作用。