Dual functions of DNA replication forks in checkpoint signaling and PCNA ubiquitination

• Published in: Cell cycle (Georgetown, Tex.) Vol. 8; no. 2; pp. 191 - 194
• Main Authors: Yang, Xiaohong H., Zou, Lee
• Format: Journal Article
• Language: English
• Published: United States Taylor & Francis 15.01.2009
• Subjects: Animals; Binding; Biology; Bioscience; Calcium; Cancer; Cell; Cell Cycle Proteins - genetics; Cell Cycle Proteins - metabolism; Checkpoint Kinase 1; Cycle; DNA Replication - physiology; Humans; Landes; Organogenesis; Proliferating Cell Nuclear Antigen - metabolism; Protein Kinases - metabolism; Proteins; Ubiquitination - physiology
• ISSN: 1538-4101; 1551-4005
• DOI: 10.4161/cc.8.2.7357

During cell proliferation, DNA damage inflicted by intrinsic or extrinsic genotoxic stresses impose a thereat to DNA replication. The stability of the DNA replication forks that encounter DNA damage is crucial for genomic integrity. Both the ATR-regulated checkpoint pathway and the translesion DNA synthesis mediated by the ubiquitinated PCNA are important for continuous replication of damaged DNA. We have recently shown that Chk1, a key effector kinase of ATR in checkpoint response, is required for efficient PCNA ubiquitination after DNA damage. Surprisingly, the ubiquitination of PCNA is independent of ATR, but regulated by Claspin, a replication protein that mediates the activation of Chk1 by ATR. Like Claspin, Timeless and Rad17, two other Chk1 regulators at stressed replication forks, are also implicated in PCNA ubiquitination. These findings suggest that while ATR signaling and PCNA ubiquitination are two independent processes, they are mediated by a common group of proteins including Chk1 and it regulators at replication forks. Furthermore, these data raise the possibility that Chk1 and its regulators may constitute a functional module at replication forks to enable multiple stress responses.