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小鼠细胞系FM3A及其温度敏感突变体tsFT20的DNA聚合酶α、δ和ε的比较

Comparison of DNA polymerases alpha, delta, and epsilon of mouse cell line FM3A and its temperature-sensitive mutant tsFT20.

作者信息

Ikehata H

机构信息

Cellular Physiology Laboratory, Institute of Physical and Chemical Research (RIKEN), Saitama, Japan.

出版信息

Tohoku J Exp Med. 1994 Jan;172(1):65-81. doi: 10.1620/tjem.172.65.

Abstract

DNA polymerases (pol) alpha, delta and epsilon of a mouse cell line FM3A and its temperature-sensitive derivative tsFT20, which is defective in DNA replication at a non-permissive temperature, were purified by chromatographic procedures monitored by a set of relatively specific assays for the respective DNA polymerase activities. The pol epsilon activity was separated into two fractions with similar enzymatic properties except for their optimal KCl concentrations and processivities. The fractions of pol delta and epsilon were not homogeneous, but their identities were confirmed by their sensitivities to DNA polymerase inhibitors, their associated 3'-->5' exonuclease activities, optimal concentrations of salts, dependencies on the proliferating cell nuclear antigen and processivities in polymerization, which also excluded significant contamination with other DNA polymerases. Of the DNA polymerases prepared from tsFT20 cells, only pol alpha showed greatly decreased activity and remarkable sensitivity to the non-permissive temperature, demonstrating that pol delta and epsilon, the other polymerases supposed to be involved in nuclear DNA replication, are unequivocally different entities from pol alpha. The level of pol epsilon activity tsFT20 was also significantly lower than in the parental cells, suggesting cooperation and/or interaction between pol alpha and epsilon, and some relevance of pol epsilon to DNA replication.

摘要

通过一系列针对各自DNA聚合酶活性的相对特异性检测进行监测的色谱方法,纯化了小鼠细胞系FM3A及其温度敏感衍生物tsFT20中的DNA聚合酶(pol)α、δ和ε。tsFT20在非允许温度下DNA复制存在缺陷。pol ε活性被分离成两个部分,除了最佳KCl浓度和持续合成能力外,它们具有相似的酶学性质。pol δ和ε的部分并不均一,但通过它们对DNA聚合酶抑制剂的敏感性、相关的3'→5'核酸外切酶活性、盐的最佳浓度、对增殖细胞核抗原的依赖性以及聚合反应中的持续合成能力,证实了它们的身份,这也排除了其他DNA聚合酶的显著污染。在从tsFT20细胞制备的DNA聚合酶中,只有pol α表现出活性大幅下降以及对非允许温度的显著敏感性,这表明pol δ和ε这两种被认为参与核DNA复制的其他聚合酶,与pol α明显不同。tsFT20中pol ε活性水平也显著低于亲代细胞,这表明pol α和ε之间存在合作和/或相互作用,并且pol ε与DNA复制存在一定相关性。

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