Crawley Clayton D, Kang Shijun, Bernal Giovanna M, Wahlstrom Joshua S, Voce David J, Cahill Kirk E, Garofalo Andrea, Raleigh David R, Weichselbaum Ralph R, Yamini Bakhtiar
a Department of Surgery, Section of Neurosurgery ; The University of Chicago ; Chicago , IL USA.
Cell Cycle. 2015;14(4):566-76. doi: 10.4161/15384101.2014.991166.
The apical damage kinase, ATR, is activated by replication stress (RS) both in response to DNA damage and during normal S-phase. Loss of function studies indicates that ATR acts to stabilize replication forks, block cell cycle progression and promote replication restart. Although checkpoint failure and replication fork collapse can result in cell death, no direct cytotoxic pathway downstream of ATR has previously been described. Here, we show that ATR directly reduces survival by inducing phosphorylation of the p50 (NF-κB1, p105) subunit of NF-кB and moreover, that this response is necessary for genome maintenance independent of checkpoint activity. Cell free and in vivo studies demonstrate that RS induces phosphorylation of p50 in an ATR-dependent but DNA damage-independent manner that acts to modulate NF-кB activity without affecting p50/p65 nuclear translocation. This response, evident in human and murine cells, occurs not only in response to exogenous RS but also during the unperturbed S-phase. Functionally, the p50 response results in inhibition of anti-apoptotic gene expression that acts to sensitize cells to DNA strand breaks independent of damage repair. Ultimately, loss of this pathway causes genomic instability due to the accumulation of chromosomal breaks. Together, the data indicate that during S-phase ATR acts via p50 to ensure that cells with elevated levels of replication-associated DNA damage are eliminated.
顶端损伤激酶ATR在DNA损伤应答以及正常S期均会被复制应激(RS)激活。功能缺失研究表明,ATR可稳定复制叉、阻断细胞周期进程并促进复制重启。尽管检查点功能障碍和复制叉崩溃会导致细胞死亡,但此前尚未描述过ATR下游直接的细胞毒性途径。在此,我们表明ATR通过诱导NF-κB的p50(NF-κB1,p105)亚基磷酸化直接降低细胞存活率,此外,这种反应对于不依赖检查点活性的基因组维持是必需的。无细胞和体内研究表明,RS以依赖ATR但不依赖DNA损伤的方式诱导p50磷酸化,该方式可调节NF-κB活性而不影响p50/p65核转位。这种反应在人和小鼠细胞中均很明显,不仅对外源RS有反应,在未受干扰的S期也会出现。在功能上,p50反应会抑制抗凋亡基因表达,使细胞对DNA链断裂敏感,且不依赖损伤修复。最终,该途径的缺失会因染色体断裂的积累导致基因组不稳定。总之,数据表明在S期,ATR通过p50发挥作用,以确保消除复制相关DNA损伤水平升高的细胞。