Dissemin is shutting down on January 1st, 2025

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American Association for the Advancement of Science, Science, 6567(374), 2021

DOI: 10.1126/science.abj3624

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A prenylated dsRNA sensor protects against severe COVID-19

Journal article published in 2021 by Arthur Wickenhagen ORCID, Elena Sugrue, Spyros Lytras, Srikeerthana Kuchi, Matthew L. Turnbull, Marko Noerenberg, Colin Loney, J. Kenneth Baillie, Vanessa Herder, Rute M. Pinto, Louisa Iselin, J. Y. Lee, Natasha Palmalux, Jay Allan, Innes Jarmson and other authors.
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Data provided by SHERPA/RoMEO

Abstract

The bat connection The heterogeneity of COVID-19 makes it challenging to predict the course of infection in an individual. Upon virus infection, interferons (IFNs) generate the initial signals for cellular defenses. Knowing that defects in IFN signaling are associated with more severe COVID-19, Wickenhagen et al . used IFN-stimulated gene expression screening on human lung cells from which they identified a gene for 2′-5′-oligoadenylate synthetase 1 (OAS1) (see the Perspective by Schoggins). OAS1 stimulates RNase L to inhibit the virus with a surprising degree of specificity, targeting the membranous organelles in which it replicates. In most mammals, OAS1 is attached to membranes by a prenyl group. However, billions of humans do not have the prenylated OAS1 haplotype, including many experiencing severe COVID-19. The same is true for horseshoe bats, prolific sources of betacoronaviruses, because of an ancient retrotransposition event. —CA