Bosco Emily E, Knudsen Erik S
Department of Cell Biology, Vontz Center for Molecular Studies, University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Nucleic Acids Res. 2005 Mar 14;33(5):1581-92. doi: 10.1093/nar/gki283. Print 2005.
The retinoblastoma tumor suppressor (RB) is functionally inactivated in the majority of cancers and is a critical mediator of DNA damage checkpoints. Despite the critical importance of RB function in tumor suppression, the coordinate impact of RB loss on the response to environmental and therapeutic sources of damage has remained largely unexplored. Here, we utilized a conditional knockout system to ablate RB in adult fibroblasts. This model system enabled us to investigate the temporal role of RB loss on cell cycle checkpoints and DNA damage repair following ultraviolet (UV) and ionizing radiation (IR) damage. We demonstrate that RB loss compromises rapid cell cycle arrest following UV and IR exposure in adult primary cells. Detailed kinetic analysis of the checkpoint response revealed that disruption of the checkpoint is concomitant with RB target gene deregulation, and is not simply a manifestation of chronic RB loss. RB loss had a differential effect upon repair of the major DNA lesions induced by IR and UV. Whereas RB did not affect resolution of DNA double-strand breaks, RB-deficient cells exhibited accelerated repair of pyrimidine pyrimidone photoproducts (6-4 PP). In parallel, this repair was coupled with enhanced expression of specific factors and the behavior of proliferating cell nuclear antigen (PCNA) recruitment to replication and repair foci. Thus, RB loss and target gene deregulation hastens the repair of specific lesions distinct from its ubiquitous role in checkpoint abrogation.
视网膜母细胞瘤肿瘤抑制因子(RB)在大多数癌症中功能失活,是DNA损伤检查点的关键调节因子。尽管RB功能在肿瘤抑制中至关重要,但RB缺失对环境和治疗性损伤源反应的协同影响在很大程度上仍未得到探索。在这里,我们利用条件性敲除系统在成年成纤维细胞中敲除RB。该模型系统使我们能够研究RB缺失在紫外线(UV)和电离辐射(IR)损伤后对细胞周期检查点和DNA损伤修复的时间作用。我们证明,RB缺失会损害成年原代细胞在UV和IR照射后快速的细胞周期停滞。对检查点反应的详细动力学分析表明,检查点的破坏与RB靶基因失调同时发生,而不仅仅是慢性RB缺失的表现。RB缺失对IR和UV诱导的主要DNA损伤的修复有不同的影响。虽然RB不影响DNA双链断裂的修复,但RB缺陷细胞表现出嘧啶嘧啶酮光产物(6-4PP)的加速修复。同时,这种修复与特定因子的表达增强以及增殖细胞核抗原(PCNA)募集到复制和修复位点的行为相关。因此,RB缺失和靶基因失调加速了特定损伤的修复,这与其在检查点废除中的普遍作用不同。