Tuusa J, Uitto L, Syväoja J E
Biocenter Oulu, University of Oulu, Finland.
Nucleic Acids Res. 1995 Jun 25;23(12):2178-83. doi: 10.1093/nar/23.12.2178.
In order to shed light on the role of mammalian DNA polymerase epsilon we studied the expression of mRNA for the human enzyme during cell proliferation and during the cell cycle. Steady-state levels of mRNA encoding DNA polymerase epsilon were elevated dramatically when quiescent (G0) cells were stimulated to proliferate (G1/S) in a similar manner to those of DNA polymerase alpha. Message levels of DNA polymerase beta were unchanged in similar experiments. The concentration of immunoreactive DNA polymerase epsilon was also much higher in extracts from proliferating tissues than in those from non-proliferating or slowly proliferating tissues. The level of DNA polymerase epsilon mRNA in actively cycling cells synchronized with nocodazole and in cells fractionated by counterflow centrifugal elutriation showed weaker variation, being at its highest at the G1/S stage boundary. The results presented strongly suggest that mammalian DNA polymerase epsilon is involved in the replication of chromosomal DNA and/or in a repair process that may be substantially activated during the replication of chromosomal DNA. A hypothetical role for DNA polymerase epsilon in a repair process coupled to replication is discussed.
为了阐明哺乳动物DNA聚合酶ε的作用,我们研究了人类该酶的mRNA在细胞增殖过程和细胞周期中的表达情况。当静止(G0)细胞受到刺激开始增殖(G1/S)时,编码DNA聚合酶ε的mRNA的稳态水平大幅升高,与DNA聚合酶α的情况类似。在类似实验中,DNA聚合酶β的信息水平没有变化。与非增殖或缓慢增殖组织的提取物相比,增殖组织提取物中免疫反应性DNA聚合酶ε的浓度也高得多。用诺考达唑同步化的活跃循环细胞以及通过逆流离心淘析法分离的细胞中,DNA聚合酶ε mRNA的水平变化较弱,在G1/S期边界时最高。所呈现的结果强烈表明,哺乳动物DNA聚合酶ε参与染色体DNA的复制和/或参与在染色体DNA复制过程中可能被显著激活的修复过程。文中讨论了DNA聚合酶ε在与复制相关的修复过程中的假设作用。