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首页> 外文期刊>Journal of Virology >Functional Regulation of an Autographa californica Nucleopolyhedrovirus-Encoded MicroRNA, AcMNPV-miR-1, in Baculovirus Replication
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Functional Regulation of an Autographa californica Nucleopolyhedrovirus-Encoded MicroRNA, AcMNPV-miR-1, in Baculovirus Replication

机译:功能性监管的Autographa californicaNucleopolyhedrovirus-Encoded微rna,AcMNPV-miR-1,杆状病毒复制

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摘要

An Autographa californica nucleopolyhedrovirus-encoded microRNA (miRNA), AcMNPV-miR-1, downregulates the ac94 gene, reducing the production of infectious budded virions and accelerating the formation of occlusion-derived virions. In the current study, four viruses that constitutively overexpress AcMNPV-miR-1 were constructed to further explore the function of the miRNA. In addition to the ac94 gene, two new viral gene targets (ac18 and ac95) of AcMNPV-miR-1 were identified, and the possible interacting proteins were verified and tested. In the context of AcMNPV-miR-1 overexpression, ac18 was slightly upregulated, and ac95 was downregulated. Several interacting proteins were identified, and a functional pathway for AcMNPV-miR-1 was deduced. AcMNPV-miR-1 overexpression decreased budded virus infectivity, reduced viral DNA replication, accelerated polyhedron formation, and promoted viral infection efficiency in Trichoplusia ni larvae, suggesting that AcMNPV-miR-1 restrains virus infection of cells but facilitates virus infection of larvae.
机译:一个Autographa californicanucleopolyhedrovirus-encoded微rna (microRNA的),AcMNPV-miR-1,会使ac94基因,减少感染植物发芽的生产病毒粒子,加快形成occlusion-derived病毒粒子。四个既定的过多表达的病毒AcMNPV-miR-1构造进一步探索microrna的功能。ac94基因,两个新病毒基因(ac18和目标ac95) AcMNPV-miR-1被确定,可能的蛋白质被验证和互动测试。超表达,ac18略调节,ac95表达下调。蛋白质,和功能推导了AcMNPV-miR-1通路。AcMNPV-miR-1过度降低发了芽的病毒的传染性,减少病毒DNA复制,加速多面体的形成和推广病毒感染效率Trichoplusia倪幼虫,表明AcMNPV-miR-1抑制病毒感染的细胞,但促进了病毒感染的幼虫。

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