DNA聚合酶
DNA钳
聚合酶
DNA聚合酶mu
DNA聚合酶Ⅱ
生物
分子生物学
DNA
DNA聚合酶Ⅰ
增殖细胞核抗原
细胞生物学
DNA修复
DNA聚合酶δ
底漆(化妆品)
遗传学
化学
细菌圆形染色体
聚合酶链反应
逆转录酶
基因
有机化学
作者
Karl E. Zahn,April M. Averill,Pierre Aller,Richard D. Wood,Sylvie Doublié
摘要
DNA polymerase θ protects against genomic instability via an alternative end-joining repair pathway for DNA double-strand breaks. Polymerase θ is overexpressed in breast, lung and oral cancers, and reduction of its activity in mammalian cells increases sensitivity to double-strand break-inducing agents, including ionizing radiation. Reported here are crystal structures of the C-terminal polymerase domain from human polymerase θ, illustrating two potential modes of dimerization. One structure depicts insertion of ddATP opposite an abasic-site analog during translesion DNA synthesis. The second structure describes a cognate ddGTP complex. Polymerase θ uses a specialized thumb subdomain to establish unique upstream contacts to the primer DNA strand, including an interaction with the 3'-terminal phosphate from one of five distinctive insertion loops. These observations demonstrate how polymerase θ grasps the primer to bypass DNA lesions or extend poorly annealed DNA termini to mediate end-joining.
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