Isbell R J, Fowler R G
Department of Biological Sciences, San Jose State University, CA 95192.
Mutat Res. 1989 Aug;213(2):149-56. doi: 10.1016/0027-5107(89)90146-2.
Escherichia coli strains carrying the temperature-dependent dnaQ49 allele are strong mutators at 37 degrees C. Since the dnaQ49 gene encodes the epsilon subunit of DNA polymerase III, it is thought that the large number of errors results in part from impaired proofreading activity during DNA replication. We have examined dnaQ49-induced reversion patterns of defined trpA alleles to determine the kinds of errors produced by dnaQ49 at 30 degrees C and 37 degrees C. We found that at 37 degrees C dnaQ49 produced all types of base-pair substitutions in addition to frameshifts with transitions generally occurring more frequently than transversions. This generalized mutator activity is very similar to that displayed in rich medium by mutD5, another mutator allele at the dnaQ locus. However, when dnaQ49 strains were cultured at 30 degrees C, not only were reversion frequencies much lower than at 37 degrees C, but in addition, the spectrum was altered. Transversions became proportionally more prevalent in the reversion spectra at the lower temperature. We suggest the possibility that at 37 degrees C dnaQ49 results in defective proofreading and methyl-directed postreplicative mismatch repair, while at 30 degrees C mismatch repair is fully and proofreading partially restored.
携带温度依赖性 dnaQ49 等位基因的大肠杆菌菌株在 37 摄氏度时是强诱变剂。由于 dnaQ49 基因编码 DNA 聚合酶 III 的 ε 亚基,因此认为大量错误部分是由于 DNA 复制过程中校对活性受损所致。我们检查了 dnaQ49 诱导的特定 trpA 等位基因的回复模式,以确定 dnaQ49 在 30 摄氏度和 37 摄氏度时产生的错误类型。我们发现,在 37 摄氏度时,dnaQ49 除了产生移码突变外,还产生了所有类型的碱基对替换,其中转换通常比颠换更频繁发生。这种普遍的诱变活性与 dnaQ 位点的另一个诱变等位基因 mutD5 在丰富培养基中表现出的活性非常相似。然而,当 dnaQ49 菌株在 30 摄氏度下培养时,不仅回复频率远低于 37 摄氏度,而且突变谱也发生了改变。在较低温度下,颠换在回复谱中变得相对更普遍。我们认为,在 37 摄氏度时,dnaQ49 导致校对缺陷和甲基导向的复制后错配修复缺陷,而在 30 摄氏度时,错配修复完全恢复,校对部分恢复。