Chan Cecilia Y, Galli Alvaro, Schiestl Robert H
Department of Pathology and Radiation Oncology, David Geffen School of Medicine at UCLA, University of California-Los Angeles, 650 Charles E. Young Drive South, Los Angeles, CA 90095, USA.
DNA Repair (Amst). 2008 Sep 1;7(9):1531-41. doi: 10.1016/j.dnarep.2008.05.008. Epub 2008 Jul 7.
Nonhomologous end joining connects DNA ends in the absence of extended sequence homology and requires removal of mismatched DNA ends and gap-filling synthesis prior to a religation step. Pol4 within the Pol X family is the only polymerase known to be involved in end processing during nonhomologous end joining in yeast. The Saccharomyces cerevisiae POL3/CDC2 gene encodes polymerase delta that is involved in DNA replication and other DNA repair processes. Here, we show that POL3 is involved in nonhomologous end joining using a plasmid-based end-joining assay in yeast, in which the pol3-t mutation caused a 1.9- to 3.2-fold decrease in the end-joining efficiency of partially compatible 5' or 3' ends, or incompatible ends, similar to the pol4 mutant. The pol3-t pol4 double mutation showed a synergistic decrease in the efficiency of NHEJ with partially compatible 5' ends or incompatible ends. Sequence analysis of the rejoined junctions recovered from the wild-type cells and mutants indicated that POL3 is required for gap filling at 3' overhangs, but not 5' overhangs during POL4-independent nonhomologous end joining. We also show that either Pol3 or Pol4 is required for simple religation of compatible or blunt ends. These results suggest that Pol3 has a generalized function in end joining in addition to its role in gap filling at 3' overhangs to enhance the overall efficiency of nonhomologous end joining. Moreover, the decreased end-joining efficiency seen in the pol3-t mutant was not due to S-phase arrest associated with the mutant. Taken together, our genetic evidence supports a novel role of Pol3 in nonhomologous end joining that facilitates gap filling at 3' overhangs in the absence of Pol4 to maintain genomic integrity.
非同源末端连接在没有长序列同源性的情况下连接DNA末端,并且在重新连接步骤之前需要去除错配的DNA末端并进行缺口填充合成。Pol X家族中的Pol4是已知参与酵母非同源末端连接过程中末端加工的唯一聚合酶。酿酒酵母POL3/CDC2基因编码参与DNA复制和其他DNA修复过程的聚合酶δ。在这里,我们使用酵母中基于质粒的末端连接试验表明POL3参与非同源末端连接,其中pol3-t突变导致部分兼容的5'或3'末端或不兼容末端的末端连接效率降低1.9至3.2倍,类似于pol4突变体。pol3-t pol4双突变在具有部分兼容的5'末端或不兼容末端的NHEJ效率上表现出协同降低。从野生型细胞和突变体中回收的重新连接接头的序列分析表明,在不依赖POL4的非同源末端连接过程中,POL3是3'突出端缺口填充所必需的,但不是5'突出端。我们还表明,兼容或平端的简单重新连接需要Pol3或Pol4。这些结果表明,Pol3除了在3'突出端缺口填充中发挥作用以提高非同源末端连接的整体效率外,在末端连接中还具有广泛的功能。此外,pol3-t突变体中观察到的末端连接效率降低不是由于与该突变体相关的S期停滞。综上所述,我们的遗传证据支持Pol3在非同源末端连接中的新作用,即在没有Pol4的情况下促进3'突出端的缺口填充以维持基因组完整性。