Lieberman Howard B, Panigrahi Sunil K, Hopkins Kevin M, Wang Li, Broustas Constantinos G
a Center for Radiological Research, Columbia University College of Physicians and Surgeons, New York, New York 10032; and.
b Department of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, New York 10032.
Radiat Res. 2017 Apr;187(4):424-432. doi: 10.1667/RR003CC.1. Epub 2017 Jan 31.
The way cells respond to DNA damage is important since inefficient repair or misrepair of lesions can have deleterious consequences, including mutation, genomic instability, neurodegenerative disorders, premature aging, cancer or death. Whether damage occurs spontaneously as a byproduct of normal metabolic processes, or after exposure to exogenous agents, cells muster a coordinated, complex DNA damage response (DDR) to mitigate potential harmful effects. A variety of activities are involved to promote cell survival, and include DNA repair, DNA damage tolerance, as well as transient cell cycle arrest to provide time for repair before entry into critical cell cycle phases, an event that could be lethal if traversal occurs while damage is present. When such damage is prolonged or not repairable, senescence, apoptosis or autophagy is induced. One major level of DDR regulation occurs via the orchestrated transcriptional control of select sets of genes encoding proteins that mediate the response. p53 is a transcription factor that transactivates specific DDR downstream genes through binding DNA consensus sequences usually in or near target gene promoter regions. The profile of p53-regulated genes activated at any given time varies, and is dependent upon type of DNA damage or stress experienced, exact composition of the consensus DNA binding sequence, presence of other DNA binding proteins, as well as cell context. RAD9 is another protein critical for the response of cells to DNA damage, and can also selectively regulate gene transcription. The limited studies addressing the role of RAD9 in transcription regulation indicate that the protein transactivates at least one of its target genes, p21/waf1/cip1, by binding to DNA sequences demonstrated to be a p53 response element. NEIL1 is also regulated by RAD9 through a similar DNA sequence, though not yet directly verified as a bonafide p53 response element. These findings suggest a novel pathway whereby p53 and RAD9 control the DDR through a shared mechanism involving an overlapping network of downstream target genes. Details and unresolved questions about how these proteins coordinate or compete to execute the DDR through transcriptional reprogramming, as well as biological implications, are discussed.
细胞对DNA损伤的反应方式至关重要,因为损伤修复效率低下或错误修复会产生有害后果,包括突变、基因组不稳定、神经退行性疾病、早衰、癌症或死亡。无论损伤是作为正常代谢过程的副产物自发发生,还是在接触外源性因素后发生,细胞都会启动协调、复杂的DNA损伤反应(DDR)以减轻潜在的有害影响。多种活动参与其中以促进细胞存活,包括DNA修复、DNA损伤耐受,以及短暂的细胞周期停滞,以便在进入关键细胞周期阶段之前提供修复时间,如果在损伤存在时进行细胞周期进程,可能会导致致命后果。当这种损伤持续存在或无法修复时,会诱导细胞衰老、凋亡或自噬。DDR调控的一个主要层面是通过对编码介导该反应的蛋白质的特定基因集进行精心的转录控制来实现的。p53是一种转录因子,它通过结合通常位于靶基因启动子区域内或附近的DNA共有序列来反式激活特定的DDR下游基因。在任何给定时间激活的p53调控基因谱各不相同,并且取决于所经历的DNA损伤或应激类型、共有DNA结合序列的确切组成、其他DNA结合蛋白的存在以及细胞背景。RAD9是另一种对细胞对DNA损伤的反应至关重要的蛋白质,它也可以选择性地调节基因转录。关于RAD9在转录调控中作用的有限研究表明,该蛋白通过结合被证明是p53反应元件的DNA序列来反式激活其至少一个靶基因p21/waf1/cip1。NEIL1也通过类似的DNA序列受RAD9调控,尽管尚未直接验证其为真正的p53反应元件。这些发现提示了一种新途径,即p53和RAD9通过涉及下游靶基因重叠网络的共享机制来控制DDR。本文讨论了这些蛋白质如何通过转录重编程协调或竞争以执行DDR的细节和未解决的问题,以及生物学意义。