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病毒:颠覆RNA周转

Viruses: overturning RNA turnover.

作者信息

Sokoloski Kevin J, Wilusz Carol J, Wilusz Jeffrey

机构信息

Colorado State University, Department of Microbiology, Immunology and Pathology, Fort Collins, Colorado 80523-1682, USA.

出版信息

RNA Biol. 2006 Oct;3(4):140-4. doi: 10.4161/rna.3.4.4076. Epub 2006 Oct 27.

Abstract

It is becoming clear that viruses interface with the mRNA decay machinery in a variety of ways during an infection. First, RNA viruses in particular must evade the mRNA decay machinery long enough to replicate and establish infection. Second, many viruses usurp or augment cellular mRNA decay pathways to regulate or selectively express their own genes, often inducing massive decay of the host transcripttome. Finally, temporal progression of a viral infection can depend on regulated decay of specific viral transcripts. Therefore, in order to fully understand viral biology, we must take into account the interactions between viruses and the mRNA decay machinery. This approach gives insights into regulatory mechanisms of cellular mRNA decay, as well as reveals novel ways to influence the outcome of viral infections.

摘要

越来越明显的是,病毒在感染过程中以多种方式与mRNA衰变机制相互作用。首先,特别是RNA病毒必须长时间避开mRNA衰变机制,以便进行复制并建立感染。其次,许多病毒篡夺或增强细胞mRNA衰变途径,以调节或选择性表达它们自己的基因,常常诱导宿主转录组的大量衰变。最后,病毒感染的时间进程可能取决于特定病毒转录本的调控衰变。因此,为了全面了解病毒生物学,我们必须考虑病毒与mRNA衰变机制之间的相互作用。这种方法有助于深入了解细胞mRNA衰变的调控机制,同时也揭示了影响病毒感染结果的新方法。

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