Department of Biological Sciences, University of North Carolina at Charlotte, Charlotte, NC, 28223, USA.
Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Nat Commun. 2024 Aug 7;15(1):6517. doi: 10.1038/s41467-024-50836-6.
In response to DNA double-strand breaks or oxidative stress, ATM-dependent DNA damage response (DDR) is activated to maintain genome integrity. However, it remains elusive whether and how DNA single-strand breaks (SSBs) activate ATM. Here, we provide direct evidence in Xenopus egg extracts that ATM-mediated DDR is activated by a defined SSB structure. Our mechanistic studies reveal that APE1 promotes the SSB-induced ATM DDR through APE1 exonuclease activity and ATM recruitment to SSB sites. APE1 protein can form oligomers to activate the ATM DDR in Xenopus egg extracts in the absence of DNA and can directly stimulate ATM kinase activity in vitro. Our findings reveal distinct mechanisms of the ATM-dependent DDR activation by SSBs in eukaryotic systems and identify APE1 as a direct activator of ATM kinase.
针对 DNA 双链断裂或氧化应激,ATM 依赖性 DNA 损伤反应(DDR)被激活以维持基因组完整性。然而,目前尚不清楚 DNA 单链断裂(SSB)是否以及如何激活 ATM。在这里,我们在非洲爪蟾卵提取物中提供了直接证据,表明 ATM 介导的 DDR 是由特定的 SSB 结构激活的。我们的机制研究表明,APE1 通过 APE1 核酸外切酶活性和 ATM 募集到 SSB 位点促进 SSB 诱导的 ATM DDR。APE1 蛋白可以形成寡聚体,在没有 DNA 的情况下在非洲爪蟾卵提取物中激活 ATM DDR,并可以在体外直接刺激 ATM 激酶活性。我们的发现揭示了真核系统中 ATM 依赖性 DDR 激活的不同机制,并确定 APE1 是 ATM 激酶的直接激活剂。