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Autographa californica multiple nucleopolyhedrovirus PK-1 is essential for nucleocapsid assembly

机译:加利福尼亚州Autographa多重核多角体病毒PK-1对于核衣壳组装至关重要

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摘要

PK-1 (Ac10) is a baculovirus-encoded serine/threonine kinase and its function is unclear. Our results showed that a pk-1 knockout AcMNPV failed to produce infectious progeny, while the pk-1 repair virus could rescue this defect. qPCR analysis demonstrated that pk-1 deletion did not affect viral DNA replication. Analysis of the repaired recombinants with truncated pk-1 mutants demonstrated that the catalytic domain of protein kinases of PK-1 was essential to viral infectivity. Moreover, those PK-1 mutants that could rescue the infectious BV production defect exhibited kinase activity in vitro. Therefore, it is suggested that the kinase activity of PK-1 is essential in regulating viral propagation. Electron microscopy revealed that pk-1 deletion affected the formation of normal nucleocapsids. Masses of electron-lucent tubular structures were present in cell transfected with pk-1 knockout bacmid. Therefore, PK-1 appears to phosphorylate some viral or cellular proteins that are essential for DNA packaging to regulate nucleocapsid assembly.
机译:PK-1(Ac10)是杆状病毒编码的丝氨酸/苏氨酸激酶,其功能尚不清楚。我们的结果表明,敲除pk-1的AcMNPV不能产生传染性子代,而pk-1修复病毒可以挽救该缺陷。 qPCR分析表明pk-1缺失不影响病毒DNA复制。用截短的pk-1突变体修复的重组体的分析表明PK-1的蛋白激酶的催化结构域对病毒感染性至关重要。此外,那些可以挽救传染性BV生产缺陷的PK-1突变体在体外表现出激酶活性。因此,提示PK-1的激酶活性在调节病毒繁殖中是必不可少的。电子显微镜显示,pk-1缺失影响正常核衣壳的形成。在用pk-1敲除杆状病毒质粒转染的细胞中存在大量电子透明管状结构。因此,PK-1似乎使某些病毒或细胞蛋白磷酸化,这对于DNA包装调节核壳组装至关重要。

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