Doerfler Lillian, Schmidt Kristina H
Department of Cell Biology, Microbiology and Molecular Biology, University of South Florida, Tampa, FL 33620, United States; Graduate Program in Cell and Molecular Biology, University of South Florida, Tampa, FL 33620, United States.
Department of Cell Biology, Microbiology and Molecular Biology, University of South Florida, Tampa, FL 33620, United States; Cancer Biology and Evolution Program, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612, United States.
DNA Repair (Amst). 2014 Dec;24:26-36. doi: 10.1016/j.dnarep.2014.10.004.
Exo1 belongs to the Rad2 family of structure-specific nucleases and possesses 5'-3' exonuclease activity on double-stranded DNA substrates. Exo1 interacts physically with the DNA mismatch repair (MMR) proteins Msh2 and Mlh1 and is involved in the excision of the mispaired nucleotide. Independent of its role in MMR, Exo1 contributes to long-range resection of DNA double-strand break (DSB) ends to facilitate their repair by homologous recombination (HR), and was recently identified as a component of error-free DNA damage tolerance pathways. Here, we show that Exo1 activity increases the hydroxyurea sensitivity of cells lacking Pol32, a subunit of DNA polymerases δ and ζ. Both, phospho-mimicking and dephospho-mimicking exo1 mutants act as hypermorphs, as evidenced by an increase in HU sensitivity of pol32Δ cells, suggesting that they are trapped in an active form and that phosphorylation of Exo1 at residues S372, S567, S587, S692 is necessary, but insufficient, for the accurate regulation of Exo1 activity at stalled replication forks. In contrast, neither phosphorylation status is important for Exo1's role in MMR or in the suppression of genome instability in cells lacking Sgs1 helicase. This ability of an EXO1 deletion to suppress the HU hypersensitivity of pol32Δ cells is in contrast to the negative genetic interaction between deletions of EXO1 and POL32 in MMS-treated cells as well as the role of EXO1 in DNA-damage treated rad53 and mec1 mutants.
Exo1属于结构特异性核酸酶的Rad2家族,对双链DNA底物具有5'-3'核酸外切酶活性。Exo1与DNA错配修复(MMR)蛋白Msh2和Mlh1发生物理相互作用,并参与错配核苷酸的切除。不依赖于其在MMR中的作用,Exo1有助于对DNA双链断裂(DSB)末端进行长距离切除,以促进通过同源重组(HR)进行修复,并且最近被鉴定为无错误DNA损伤耐受途径的一个组成部分。在这里,我们表明Exo1活性增加了缺乏DNA聚合酶δ和ζ的一个亚基Pol32的细胞对羟基脲的敏感性。磷酸化模拟和去磷酸化模拟的exo1突变体均表现为超形态,这通过pol32Δ细胞对HU敏感性的增加得以证明,表明它们被困在活性形式中,并且Exo1在S372、S567、S587、S692残基处的磷酸化对于在停滞的复制叉处准确调节Exo1活性是必要的,但并不充分。相比之下,磷酸化状态对于Exo1在MMR中的作用或在缺乏Sgs1解旋酶的细胞中抑制基因组不稳定性的作用均不重要。EXO1缺失抑制pol32Δ细胞对HU超敏感性的这种能力与在MMS处理的细胞中EXO1和POL32缺失之间的负遗传相互作用以及EXO1在DNA损伤处理的rad53和mec1突变体中的作用形成对比。