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Parvovirus B19 Nonstructural Protein-Induced Damage of Cellular DNA and Resultant Apoptosis

机译:细小病毒B19非结构蛋白诱导的细胞DNA损伤和导致的细胞凋亡

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摘要

Parvovirus B19 is a widespread virus with diverse clinical presentations. The viral nonstructural protein, NS1, binds to and cleaves the viral genome, and induces apoptosis when transfected into nonpermissive cells, such as hepatocytes. We hypothesized that the cytotoxicity of NS1 in such cells results from chromosomal DNA damage caused by the DNA-nicking and DNA-attaching activities of NS1. Upon testing this hypothesis, we found that NS1 covalently binds to cellular DNA and is modified by PARP, an enzyme involved in repairing single-stranded DNA nicks. We furthermore discovered that the DNA nick repair pathway initiated by poly(ADPribose)polymerase and the DNA repair pathways initiated by ATM/ATR are necessary for efficient apoptosis resulting from NS1 expression.
机译:细小病毒B19是一种广泛传播的病毒,具有多种临床表现。病毒非结构蛋白NS1结合并切割病毒基因组,并在转染入非许可细胞(例如肝细胞)时诱导凋亡。我们假设NS1在这种细胞中的细胞毒性是由NS1的DNA缺口和DNA附着活性引起的染色体DNA损伤引起的。通过检验该假设,我们发现NS1与细胞DNA共价结合并被PARP修饰,PARP是一种参与修复单链DNA缺口的酶。我们还发现,由聚(ADPribose)聚合酶引发的DNA切口修复途径和由ATM / ATR引发的DNA修复途径对于从NS1表达产生的有效凋亡是必需的。

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