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Mouse Ifit1b is a cap1-RNA-binding protein that inhibits mouse coronavirus translation and is regulated by complexing with Ifit1c.
Mears, Harriet V; Sweeney, Trevor R.
  • Mears HV; Division of Virology, Department of Pathology, University of Cambridge, Addenbrooke's Hospital, Cambridge, United Kingdom. Electronic address: hvm30@cam.ac.uk.
  • Sweeney TR; Division of Virology, Department of Pathology, University of Cambridge, Addenbrooke's Hospital, Cambridge, United Kingdom. Electronic address: ts629@cam.ac.uk.
J Biol Chem ; 295(51): 17781-17801, 2020 12 18.
Article in English | MEDLINE | ID: covidwho-985572
ABSTRACT
Knockout mouse models have been extensively used to study the antiviral activity of IFIT (interferon-induced protein with tetratricopeptide repeats). Human IFIT1 binds to cap0 (m7GpppN) RNA, which lacks methylation on the first and second cap-proximal nucleotides (cap1, m7GpppNm, and cap2, m7GpppNmNm, respectively). These modifications are signatures of "self" in higher eukaryotes, whereas unmodified cap0-RNA is recognized as foreign and, therefore, potentially harmful to the host cell. IFIT1 inhibits translation at the initiation stage by competing with the cap-binding initiation factor complex, eIF4F, restricting infection by certain viruses that possess "nonself" cap0-mRNAs. However, in mice and other rodents, the IFIT1 orthologue has been lost, and the closely related Ifit1b has been duplicated twice, yielding three paralogues Ifit1, Ifit1b, and Ifit1c. Although murine Ifit1 is similar to human IFIT1 in its cap0-RNA-binding selectivity, the roles of Ifit1b and Ifit1c are unknown. Here, we found that Ifit1b preferentially binds to cap1-RNA, whereas binding is much weaker to cap0- and cap2-RNA. In murine cells, we show that Ifit1b can modulate host translation and restrict WT mouse coronavirus infection. We found that Ifit1c acts as a stimulatory cofactor for both Ifit1 and Ifit1b, promoting their translation inhibition. In this way, Ifit1c acts in an analogous fashion to human IFIT3, which is a cofactor to human IFIT1. This work clarifies similarities and differences between the human and murine IFIT families to facilitate better design and interpretation of mouse models of human infection and sheds light on the evolutionary plasticity of the IFIT family.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Protein Biosynthesis / RNA Caps / RNA-Binding Proteins / Coronavirus / RNA Cap-Binding Proteins / Adaptor Proteins, Signal Transducing Limits: Animals / Humans Language: English Journal: J Biol Chem Year: 2020 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Protein Biosynthesis / RNA Caps / RNA-Binding Proteins / Coronavirus / RNA Cap-Binding Proteins / Adaptor Proteins, Signal Transducing Limits: Animals / Humans Language: English Journal: J Biol Chem Year: 2020 Document Type: Article