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节肢动物传播的黄病毒产生的非编码 RNA 抑制细胞外切核糖核酸酶 XRN1 并改变宿主 mRNA 的稳定性。

A noncoding RNA produced by arthropod-borne flaviviruses inhibits the cellular exoribonuclease XRN1 and alters host mRNA stability.

机构信息

Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado 80523, USA.

出版信息

RNA. 2012 Nov;18(11):2029-40. doi: 10.1261/rna.034330.112. Epub 2012 Sep 24.

Abstract

All arthropod-borne flaviviruses generate a short noncoding RNA (sfRNA) from the viral 3' untranslated region during infection due to stalling of the cellular 5'-to-3' exonuclease XRN1. We show here that formation of sfRNA also inhibits XRN1 activity. Cells infected with Dengue or Kunjin viruses accumulate uncapped mRNAs, decay intermediates normally targeted by XRN1. XRN1 repression also resulted in the increased overall stability of cellular mRNAs in flavivirus-infected cells. Importantly, a mutant Kunjin virus that cannot form sfRNA but replicates to normal levels failed to affect host mRNA stability or XRN1 activity. Expression of sfRNA in the absence of viral infection demonstrated that sfRNA formation was directly responsible for the stabilization of cellular mRNAs. Finally, numerous cellular mRNAs were differentially expressed in an sfRNA-dependent fashion in a Kunjin virus infection. We conclude that flaviviruses incapacitate XRN1 during infection and dysregulate host mRNA stability as a result of sfRNA formation.

摘要

所有节肢动物传播的黄病毒在感染过程中都会由于细胞 5' 到 3' 外切酶 XRN1 的停滞而从病毒 3' 非翻译区产生一段短的非编码 RNA (sfRNA)。我们在这里表明,sfRNA 的形成也会抑制 XRN1 的活性。感染登革热或昆津病毒的细胞会积累无帽的 mRNA,这些 mRNA 是 XRN1 通常靶向的降解中间产物。XRN1 的抑制也导致了黄病毒感染细胞中细胞 mRNA 的整体稳定性增加。重要的是,一种不能形成 sfRNA 但复制水平正常的突变型昆津病毒不能影响宿主 mRNA 的稳定性或 XRN1 的活性。在没有病毒感染的情况下表达 sfRNA 表明,sfRNA 的形成直接导致了细胞 mRNA 的稳定。最后,在昆津病毒感染中,许多细胞 mRNA 以 sfRNA 依赖的方式差异表达。我们的结论是,黄病毒在感染过程中使 XRN1 失活,并通过 sfRNA 的形成导致宿主 mRNA 稳定性失调。

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