A Bicistronic MAVS Transcript Highlights a Class of Truncated Variants in Antiviral Immunity
Author(s) -
Sky W. Brubaker,
Anna E. Gauthier,
Eric W. Mills,
Nicholas T. Ingolia,
Jonathan C. Kagan
Publication year - 2014
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2014.01.021
Subject(s) - biology , innate immune system , messenger rna , gene , translation (biology) , genetics , rna splicing , interferon , genome , protein biosynthesis , microbiology and biotechnology , rna , computational biology , immune system
Bacterial and viral mRNAs are often polycistronic. Akin to alternative splicing, alternative translation of polycistronic messages is a mechanism to generate protein diversity and regulate gene function. Although a few examples exist, the use of polycistronic messages in mammalian cells is not widely appreciated. Here we report an example of alternative translation as a means of regulating innate immune signaling. MAVS, a regulator of antiviral innate immunity, is expressed from a bicistronic mRNA encoding a second protein, miniMAVS. This truncated variant interferes with interferon production induced by full-length MAVS, whereas both proteins positively regulate cell death. To identify other polycistronic messages, we carried out genome-wide ribosomal profiling and identified a class of antiviral truncated variants. This study therefore reveals the existence of a functionally important bicistronic antiviral mRNA and suggests a widespread role for polycistronic mRNAs in the innate immune system.
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