Navas T A, Zhou Z, Elledge S J
Verna and Marrs McLean Department of Biochemistry, Baylor College of Medicine, Houston, Texas 77030.
Cell. 1995 Jan 13;80(1):29-39. doi: 10.1016/0092-8674(95)90448-4.
Inhibition of DNA synthesis induces transcription of DNA damage-inducible genes and prevents mitotic entry through the action of the S phase checkpoint. We have isolated a mutant, dun2, defective for both of these responses. DUN2 is identical to POL2, encoding DNA polymerase epsilon (pol epsilon). Unlike sad1 mutants defective for multiple cell cycle checkpoints, pol2 mutants are defective only for the S phase checkpoint and the activation of DUN1 kinase necessary for the transcriptional response to damage. Interallelic complementation and mutation analysis indicate that pol epsilon contains two separable essential domains, an N-terminal polymerase domain and a C-terminal checkpoint domain unique to epsilon polymerases. We propose that DNA pol epsilon acts as a sensor of DNA replication that coordinates the transcriptional and cell cycle responses to replication blocks.
DNA合成的抑制会诱导DNA损伤诱导基因的转录,并通过S期检查点的作用阻止有丝分裂的进入。我们分离出了一个突变体dun2,它在这两种反应中都存在缺陷。DUN2与POL2相同,编码DNA聚合酶ε(pol ε)。与多个细胞周期检查点存在缺陷的sad1突变体不同,pol2突变体仅在S期检查点以及对损伤的转录反应所必需的DUN1激酶的激活方面存在缺陷。等位基因间互补和突变分析表明,pol ε包含两个可分离的必需结构域,一个N端聚合酶结构域和一个ε聚合酶特有的C端检查点结构域。我们提出,DNA pol ε作为DNA复制的传感器,协调对复制阻滞的转录和细胞周期反应。