Institute for Molecular Virology, University of Wisconsin-Madison, Madison, WI 53706, USA.
Cellular and Molecular Biology Graduate Program, University of Wisconsin-Madison, Madison, WI 53706, USA.
Viruses. 2023 May 25;15(6):1243. doi: 10.3390/v15061243.
Minute Virus of Mice (MVM) is an autonomous parvovirus of the family that replicates in mouse cells and transformed human cells. MVM genomes localize to cellular sites of DNA damage with the help of their essential non-structural phosphoprotein NS1 to establish viral replication centers. MVM replication induces a cellular DNA damage response that is mediated by signaling through the ATM kinase pathway, while inhibiting induction of the ATR kinase signaling pathway. However, the cellular signals regulating virus localization to cellular DNA damage response sites has remained unknown. Using chemical inhibitors to DNA damage response proteins, we have discovered that NS1 localization to cellular DDR sites is independent of ATM or DNA-PK signaling but is dependent on ATR signaling. Pulsing cells with an ATR inhibitor after S-phase entry leads to attenuated MVM replication. These observations suggest that the initial localization of MVM to cellular DDR sites depends on ATR signaling before it is inactivated by vigorous virus replication.
小鼠微小病毒(MVM)是细小病毒科的自主细小病毒,在小鼠细胞和转化的人细胞中复制。MVM 基因组在其必需的非结构磷蛋白 NS1 的帮助下定位于细胞 DNA 损伤部位,以建立病毒复制中心。MVM 复制诱导细胞 DNA 损伤反应,该反应通过 ATM 激酶途径的信号转导来介导,同时抑制 ATR 激酶信号转导途径的诱导。然而,调节病毒定位到细胞 DNA 损伤反应部位的细胞信号仍然未知。我们使用化学抑制剂对 DNA 损伤反应蛋白进行研究,发现 NS1 定位于细胞 DDR 部位与 ATM 或 DNA-PK 信号无关,但依赖于 ATR 信号。在 S 期进入后用 ATR 抑制剂脉冲细胞会导致 MVM 复制减弱。这些观察结果表明,在强烈的病毒复制使其失活之前,MVM 最初定位于细胞 DDR 部位依赖于 ATR 信号。