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A putative Leishmania DNA polymerase theta protects the parasite against oxidative damage

机译:推定的利什曼原虫DNA聚合酶θ可保护寄生虫免受氧化损伤

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摘要

Leishmania infantum is a protozoan parasite that is phagocytized by human macrophages. The host macrophages kill the parasite by generating oxidative compounds that induce DNA damage. We have identified, purified and biochemically characterized a DNA polymerase θ from L. infantum (LiPolθ), demonstrating that it is a DNA-dependent DNA polymerase involved in translesion synthesis of 8oxoG, abasic sites and thymine glycol lesions. Stably transfected L. infantum parasites expressing LiPolθ were significantly more resistant to oxidative and interstrand cross-linking agents, e.g. hydrogen peroxide, cisplatin and mitomycin C. Moreover, LiPolθ-overexpressing parasites showed an increased infectivity toward its natural macrophage host. Therefore, we propose that LiPolθ is a translesion synthesis polymerase involved in parasite DNA damage tolerance, to confer resistance against macrophage aggression.
机译:婴儿利什曼原虫是被人类巨噬细胞吞噬的原生动物寄生虫。宿主巨噬细胞通过产生诱导DNA损伤的氧化化合物杀死寄生虫。我们已经鉴定,纯化和生化鉴定了来自婴儿乳杆菌的DNA聚合酶θ(LiPolθ),表明它是一种DNA依赖性DNA聚合酶,参与8oxoG,无碱基位点和胸腺嘧啶乙二醇损伤的跨病变合成。稳定转染的表达LiPolθ的婴儿乳杆菌寄生虫对氧化剂和链间交联剂(如过氧化氢,顺铂和丝裂霉素C。此外,过表达LiPolθ的寄生虫对其天然巨噬细胞宿主的感染性增强。因此,我们提出LiPolθ是一种参与寄生虫DNA损伤耐受性的跨病变合成聚合酶,以赋予对巨噬细胞侵袭的抗性。

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