Waser J, Hübscher U, Kuenzle C C, Spadari S
Eur J Biochem. 1979 Jul;97(2):361-8. doi: 10.1111/j.1432-1033.1979.tb13122.x.
DNA polymerase beta was isolated from rat cortex neurons and characterised. Its properties were strikingly similar to those of other mammalian beta-polymerases. In adult rats, this was the major DNA polymerase occurring in neuronal nuclei, which contained no alpha-polymerase, 99.2% beta-polymerase and only 0.8% gamma-polymerase. Isolated neuronal nuclei of this developmental stage were shown to perform ultraviolet-induced repair DNA synthesis in vitro. Since beta-polymerase was virtually the exclusive DNA polymerase in these nuclei it was concluded that the beta enzyme was responsible for the observed DNA repair. This was further substantiated by demonstrating a virtually complete suppression of DNA repair in irradiated nuclei by 2',3'-dideoxyribosylthymine 5'-triphosphate (d2TTP), a potent beta-polymerase inhibitor. However, the presence of minute amounts of gamma-polymerase in neuronal nuclei and its susceptibility to d2TTP did not allow one to rule out an ancillary role of DNA polymerase gamma in DNA repair. In view of the similarity of the neuronal DNA polymerase beta with all other mammalian beta-polymerases it may be speculated that the ability to perform repair DNA synthesis is not unique to the neuronal enzyme but is a general function of all beta-polymerases.
从大鼠皮质神经元中分离并鉴定了DNA聚合酶β。其特性与其他哺乳动物的β聚合酶极为相似。在成年大鼠中,这是神经元细胞核中主要存在的DNA聚合酶,其中不含α聚合酶,β聚合酶占99.2%,γ聚合酶仅占0.8%。该发育阶段分离出的神经元细胞核在体外可进行紫外线诱导的修复性DNA合成。由于β聚合酶实际上是这些细胞核中唯一的DNA聚合酶,因此得出结论,β酶负责观察到的DNA修复。通过证明2',3'-二脱氧核糖基胸腺嘧啶5'-三磷酸(d2TTP,一种有效的β聚合酶抑制剂)几乎完全抑制了受辐照细胞核中的DNA修复,这一点得到了进一步证实。然而,神经元细胞核中存在微量的γ聚合酶及其对d2TTP的敏感性,使得人们无法排除DNA聚合酶γ在DNA修复中的辅助作用。鉴于神经元DNA聚合酶β与所有其他哺乳动物β聚合酶的相似性,可以推测进行修复性DNA合成的能力并非神经元酶所特有,而是所有β聚合酶的普遍功能。