| Literature DB >> 30270045 |
Xavier Lahaye1, Matteo Gentili1, Aymeric Silvin1, Cécile Conrad1, Léa Picard2, Mabel Jouve1, Elina Zueva1, Mathieu Maurin1, Francesca Nadalin1, Gavin J Knott3, Baoyu Zhao4, Fenglei Du4, Marlène Rio5, Jeanne Amiel5, Archa H Fox6, Pingwei Li4, Lucie Etienne7, Charles S Bond3, Laurence Colleaux5, Nicolas Manel8.
Abstract
Detection of viruses by innate immune sensors induces protective antiviral immunity. The viral DNA sensor cyclic GMP-AMP synthase (cGAS) is necessary for detection of HIV by human dendritic cells and macrophages. However, synthesis of HIV DNA during infection is not sufficient for immune activation. The capsid protein, which associates with viral DNA, has a pivotal role in enabling cGAS-mediated immune activation. We now find that NONO is an essential sensor of the HIV capsid in the nucleus. NONO protein directly binds capsid with higher affinity for weakly pathogenic HIV-2 than highly pathogenic HIV-1. Upon infection, NONO is essential for cGAS activation by HIV and cGAS association with HIV DNA in the nucleus. NONO recognizes a conserved region in HIV capsid with limited tolerance for escape mutations. Detection of nuclear viral capsid by NONO to promote DNA sensing by cGAS reveals an innate strategy to achieve distinction of viruses from self in the nucleus.Entities:
Keywords: HIV-1; HIV-2; NONO; STING; cGAS; capsid; dendritic cells; innate immune sensors; innate immunity; macrophages
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Year: 2018 PMID: 30270045 DOI: 10.1016/j.cell.2018.08.062
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582