OAS proteins and cGAS: unifying concepts in sensing and responding to cytosolic nucleic acids

Veit Hornung, Rune Hartmann, Andrea Ablasser, Karl-Peter Hopfner

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    260 Citations (Scopus)

    Abstract

    Recent discoveries in the field of innate immunity have highlighted the existence of a family of nucleic acid-sensing proteins that have similar structural and functional properties. These include the well-known oligoadenylate synthase (OAS) family proteins and the recently identified OAS homologue cyclic GMP-AMP (cGAMP) synthase (cGAS). The OAS proteins and cGAS are template-independent nucleotidyltransferases that, once activated by double-stranded nucleic acids in the cytosol, produce unique classes of 2'-5'-linked second messenger molecules, which - through distinct mechanisms - have crucial antiviral functions. 2'-5'-linked oligoadenylates limit viral propagation through the activation of the enzyme RNase L, which degrades host and viral RNA, and 2'-5'-linked cGAMP activates downstream signalling pathways to induce de novo antiviral gene expression. In this Progress article, we describe the striking functional and structural similarities between OAS proteins and cGAS, and highlight their roles in antiviral immunity.

    Original languageEnglish
    JournalNature Reviews. Immunology
    Volume14
    Issue8
    Pages (from-to)521-528
    Number of pages8
    ISSN1474-1733
    DOIs
    Publication statusPublished - 18 Jul 2014

    Keywords

    • 2',5'-Oligoadenylate Synthetase
    • Adenine Nucleotides
    • Cytosol
    • DNA
    • Endoribonucleases
    • Humans
    • Immunity, Innate
    • Nucleotides, Cyclic
    • Nucleotidyltransferases
    • Oligoribonucleotides
    • RNA
    • RNA Viruses
    • RNA, Viral
    • Second Messenger Systems
    • Viruses

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