Volume 26 Issue 9 Pages May 2016 Biology Diagrams From bacteria to mammalian cells, damaged DNA is sensed and targeted by DNA repair pathways. In eukaryotes, kinases play a central role in coordinating the DNA damage response. DNA damage signaling kinases were identified over two decades ago and linked to the cell cycle checkpoint concept proposed by Weinert and Hartwell in 1988. In sum, apical kinases perform highly elaborate actions in the spatiotemporal control of checkpoint responses and DNA repair. Since checkpoint functions and early resection blockades can counteract HRโmediated DNA repair mechanisms, the ability of cells to modulate DNA damage signaling is essential for repair pathway control, and, in
ABSTRACT. Cell cycle checkpoints activated by DNA double-strand breaks (DSBs) are essential for the maintenance of the genomic integrity of proliferating cells. Following DNA damage, cells must detect the break and either transiently block cell cycle progression, to allow time for repair, or exit the cell cycle. Reversal of a DNA-damage-induced checkpoint not only requires the repair of these The damaged DNA may activate the DNA damage response signaling pathway, where DNA damage checkpoints play a central role in arresting the cell cycle and mediating the DNA repair process. The unsuccessful repairing of DNA lesions may cause apoptosis, cell death or cancer. The integrity of genomic DNA is continually monitored and DNA repair is coordinated with the cell cycle via the G1/S, intra-S phase, and G2/M checkpoints. During mitosis, communication between the mitotic checkpoint complex (MCC) and anaphase-promoting complex/cyclosome (APC/C) ensures the proper alignment and segregation of chromosomes.
Cell Cycle Regulation by Checkpoints Biology Diagrams
The signal transducers activate p53 and inactivate cyclin-dependent kinases to inhibit cell cycle progression from G1 to S (the G1/S checkpoint), DNA replication (the intra-S checkpoint), or G2 to mitosis (the G2/M checkpoint). In this review the molecular mechanisms of DNA repair and the DNA damage checkpoints in mammalian cells are analyzed. A recent study used immunofluorescence (IF) staining of repair proteins as surrogate markers to examine DSBs, SSBs, and base damages in human cells to directly visualize the induction and repair of clustered DNA lesions at the single-cell level . Results showed that a large fraction of 53BP1, XRCC1, and hOGG1 foci colocalized with another
The repair of DNA lesions that occur endogenously or in response to diverse genotoxic stresses is indispensable for genome integrity. DNA lesions activate checkpoint pathways that regulate In the meantime, an intimate relationship between mechanisms of damage checkpoint pathway, DNA damage repair, and genome stability was also uncovered. Reviewed herein are the recent findings on both the mechanisms of activation of checkpoint pathways and their coordination with DNA damage repair machinery as well as their effect on genomic