Department of Molecular Genetics and Microbiology, School of Medicine, Stony Brook University, Stony Brook, NY 11794, USA.
J Virol. 2011 May;85(9):4135-42. doi: 10.1128/JVI.02540-10. Epub 2011 Feb 23.
Adenovirus has a linear, double-stranded DNA genome that is perceived by the cellular Mre11-Rad50-Nbs1 (MRN) DNA repair complex as a double-strand break. If unabated, MRN elicits a double-strand break repair response that blocks viral DNA replication and ligates the viral genomes into concatemers. There are two sets of early viral proteins that inhibit the MRN complex. The E1B-55K/E4-ORF6 complex recruits an E3 ubiquitin ligase and targets MRN proteins for proteasome-dependent degradation. The E4-ORF3 protein inhibits MRN through sequestration. The mechanism that prevents MRN recognition of the viral genome prior to the expression of these early proteins was previously unknown. Here we show a temporal correlation between the loss of viral core protein VII from the adenovirus genome and a gain of checkpoint signaling due to the double-strand break repair response. While checkpoint signaling corresponds to the recognition of the viral genome, core protein VII binding to and checkpoint signaling at viral genomes are largely mutually exclusive. Transcription is known to release protein VII from the genome, and the inhibition of transcription shows a decrease in checkpoint signaling. Finally, we show that the nuclease activity of Mre11 is dispensable for the inhibition of viral DNA replication during a DNA damage response. These results support a model involving the protection of the incoming viral genome from checkpoint signaling by core protein VII and suggest that the induction of an MRN-dependent DNA damage response may inhibit adenovirus replication by physically masking the origins of DNA replication rather than altering their integrity.
腺病毒具有线性双链 DNA 基因组,该基因组被细胞的 Mre11-Rad50-Nbs1 (MRN) 双链断裂修复复合物识别为双链断裂。如果不加以控制,MRN 会引发双链断裂修复反应,阻止病毒 DNA 复制并将病毒基因组连接成串联体。有两组早期病毒蛋白抑制 MRN 复合物。E1B-55K/E4-ORF6 复合物招募一种 E3 泛素连接酶,并将 MRN 蛋白靶向蛋白酶体依赖性降解。E4-ORF3 蛋白通过隔离来抑制 MRN。在表达这些早期蛋白之前,防止 MRN 识别病毒基因组的机制以前是未知的。在这里,我们显示了腺病毒基因组中病毒核心蛋白 VII 的丢失与由于双链断裂修复反应而导致的检查点信号获得之间的时间相关性。虽然检查点信号对应于病毒基因组的识别,但核心蛋白 VII 与病毒基因组的结合和检查点信号在很大程度上是相互排斥的。转录已知可从基因组中释放蛋白 VII,并且转录抑制显示检查点信号减少。最后,我们表明,在 DNA 损伤反应期间,Mre11 的核酸酶活性对于抑制病毒 DNA 复制是可有可无的。这些结果支持了一种模型,即核心蛋白 VII 可保护进入的病毒基因组免受检查点信号的影响,并表明诱导 MRN 依赖性 DNA 损伤反应可能通过物理掩盖 DNA 复制的起点而不是改变其完整性来抑制腺病毒复制。