作者: Kim Engels , Michele Giannattasio , Marco Muzi-Falconi , Massimo Lopes , Stefano Ferrari
DOI: 10.1371/JOURNAL.PGEN.1001367
关键词:
摘要: Replication fork integrity, which is essential for the maintenance of genome stability, monitored by checkpoint-mediated phosphorylation events. 14-3-3 proteins are able to bind phosphorylated and were shown play an undefined role under DNA replication stress. Exonuclease 1 (Exo1) processes stalled forks in checkpoint-defective yeast cells. We now identify as vivo interaction partners Exo1, both mammalian Yeast 14-3-3–deficient cells fail induce Mec1–dependent Exo1 hyperphosphorylation accumulate Exo1–dependent ssDNA gaps at forks, revealed electron microscopy. This leads persistent checkpoint activation exacerbated recovery defects. Moreover, using bi-dimensional electrophoresis, we show that promote progression limiting nucleotide concentrations. propose assist controlling status additional unknown targets, promoting progression, restart response