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An Endonuclease Switching Mechanism in the Virion RNA and cRNA Promoters of Thogoto Orthomyxovirus

机译:Thogoto正粘病毒的病毒RNA和cRNA启动子中的核酸内切酶转换机制

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摘要

An in vitro assay was developed to investigate endonuclease activity of Thogoto virus, a tick-borne orthomyxovirus. Endonuclease activity relied on an interaction between the 3′ and 5′ termini of virion RNA (vRNA) and not those of cRNA. Evidence was obtained that cap structures are cleaved directly from cap donors and that cleavage does not occur after pyrimidines. A 5′ hook structure, present in the vRNA promoter but not the cRNA promoter, was introduced into cRNA promoter mutants. These mutants stimulated endonuclease activity, although at levels slightly lower than that of vRNA. The ability of the cRNA promoter to stimulate endonuclease activity when mutated to contain a 5′ hook structure indicates that this structure constitutes a switching mechanism for endonuclease activity between the vRNA and cRNA promoters.
机译:开发了一种体外测定法,以研究壁虱传播的正粘病毒Thogoto病毒的核酸内切酶活性。核酸内切酶活性依赖于病毒体RNA(vRNA)3'和5'末端之间的相互作用,而不依赖于cRNA的相互作用。获得的证据表明,帽结构直接从帽供体上裂解,并且在嘧啶之后不会发生裂解。将存在于vRNA启动子而不是cRNA启动子的5'钩结构引入cRNA启动子突变体。这些突变体刺激了核酸内切酶活性,尽管其水平略低于vRNA。当突变为包含5'钩结构时,cRNA启动子刺激内切核酸酶活性的能力表明该结构构成了vRNA和cRNA启动子之间内切核酸酶活性的转换机制。

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