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Corrigendum: A diverse range of gene products are effectors of the type I interferon antiviral response.

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TLDR
In this paper, the authors used the WNV-GFP stock used in the data set (Fig. 2 and Supplementary Table 8 of the original Letter) for West Nile virus (WNV) in this Letter was actually Venezuelan equine encephalitis virus (VEEV)-GFP.
Abstract
Nature 472, 481–485 (2011); doi:10.1038/nature09907 We have recently discovered that the WNV-GFP stock used in the data set (Fig. 2 and Supplementary Table 8 of the original Letter) for West Nile virus (WNV) in this Letter was actually Venezuelan equine encephalitis virus (VEEV-GFP). The error has been tracked to a technical mistake made during the virus production process.

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Regulation of type I interferon responses

TL;DR: In this paper, the authors summarize the signalling and epigenetic mechanisms that regulate type I IFN-induced STAT activation and ISG transcription and translation and conclude that these regulatory mechanisms determine the biological outcomes of type I ILN responses and whether pathogens are cleared effectively or chronic infection or autoimmune disease ensues.
Journal ArticleDOI

Interferon-Stimulated Genes: A Complex Web of Host Defenses

TL;DR: This review begins by introducing interferon (IFN) and the JAK-STAT signaling pathway to highlight features that impact ISG production and describes ways in which ISGs both enhance innate pathogen-sensing capabilities and negatively regulate signaling through the Jak-STAT pathway.
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Regulation and function of the cGAS-STING pathway of cytosolic DNA sensing

TL;DR: Recent advances in understanding of the cGAS–STING pathway are reviewed, focusing on the regulatory mechanisms and roles of this pathway in heath and disease.
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Cytosolic Sensing of Viruses

TL;DR: Recent advances in the molecular understanding of cytosolic nucleic acid detection and its evasion by viruses are detailed.
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Journal ArticleDOI

A diverse range of gene products are effectors of the type I interferon antiviral response

TL;DR: It is shown that different viruses are targeted by unique sets of ISGs, and that each viral species is susceptible to multiple antiviral genes, which together encompass a range of inhibitory activities.
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