Pathobiology Area Graduate Program, University of Missouri-Columbia, Columbia, MO 65211, USA.
Christopher S. Bond Life Sciences Center, University of Missouri-Columbia, Columbia, MO 65211, USA.
Hum Mol Genet. 2022 Mar 21;31(6):985-998. doi: 10.1093/hmg/ddab300.
Nuclear DNA viruses simultaneously access cellular factors that aid their life cycle while evading inhibitory factors by localizing to distinct nuclear sites. Adeno-associated viruses (AAVs), which are Dependoviruses in the family Parvovirinae, are non-enveloped icosahedral viruses, which have been developed as recombinant AAV vectors to express transgenes. AAV2 expression and replication occur in nuclear viral replication centers (VRCs), which relies on cellular replication machinery as well as coinfection by helper viruses such as adenoviruses or herpesviruses, or exogenous DNA damage to host cells. AAV2 infection induces a complex cellular DNA damage response (DDR), in response to either viral DNA or viral proteins expressed in the host nucleus during infection, where VRCs co-localized with DDR proteins. We have previously developed a modified iteration of a viral chromosome conformation capture (V3C-seq) assay to show that the autonomous parvovirus minute virus of mice localizes to cellular sites of DNA damage to establish and amplify its replication. Similar V3C-seq assays to map AAV2 show that the AAV2 genome co-localized with cellular sites of DNA damage under both non-replicating and replicating conditions. The AAV2 non-structural protein Rep 68/78, also localized to cellular DDR sites during both non-replicating and replicating infections, and also when ectopically expressed. Ectopically expressed Rep could be efficiently re-localized to DDR sites induced by micro-irradiation. Recombinant AAV2 gene therapy vector genomes derived from AAV2 localized to sites of cellular DNA damage to a lesser degree, suggesting that the inverted terminal repeat origins of replication were insufficient for targeting.
核 DNA 病毒同时利用有助于其生命周期的细胞因子,同时通过定位于不同的核部位来逃避抑制因子。腺相关病毒(AAV)是细小病毒科依赖病毒科的非包膜二十面体病毒,已被开发为重组 AAV 载体来表达转基因。AAV2 的表达和复制发生在核病毒复制中心(VRC)中,这依赖于细胞复制机制以及辅助病毒(如腺病毒或疱疹病毒)的共感染,或宿主细胞的外源性 DNA 损伤。AAV2 感染诱导复杂的细胞 DNA 损伤反应(DDR),以响应病毒 DNA 或感染期间在宿主核中表达的病毒蛋白,其中 VRC 与 DDR 蛋白共定位。我们之前开发了一种改良的病毒染色体构象捕获(V3C-seq)检测方法的迭代,以显示自主细小病毒小鼠微小病毒定位于细胞 DNA 损伤部位以建立和扩增其复制。类似的用于绘制 AAV2 的 V3C-seq 检测表明,AAV2 基因组在非复制和复制条件下均与细胞 DNA 损伤部位共定位。AAV2 非结构蛋白 Rep68/78 在非复制和复制感染期间以及异位表达时也定位于细胞 DDR 部位。异位表达的 Rep 可以有效地重新定位到微照射诱导的 DDR 部位。源自 AAV2 的重组 AAV2 基因治疗载体基因组定位于细胞 DNA 损伤部位的程度较小,表明复制起始的倒置末端重复序列不足以为靶向。