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PQBP1 Is a Proximal Sensor of the cGAS-Dependent Innate Response to HIV-1
Author(s) -
Sunnie M. Yoh,
Monika Schneider,
Janna Seifried,
Stephen Soonthornvacharin,
Rana Elias Akleh,
Kevin C. Olivieri,
Paul D. De Jesus,
Chunhai Ruan,
Elisa de Castro,
Pedro A. Ruiz,
David Germanaud,
Vincent des Portes,
Adolfo Garcı́a-Sastre,
Renate König,
Sumit K. Chanda
Publication year - 2015
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.2015.04.050
Subject(s) - innate immune system , biology , irf3 , intrinsic immunity , virology , immune system , acquired immune system , immunology , immunity , microbiology and biotechnology
Dendritic cells (DCs) play a critical role in the immune response to viral infection through the facilitation of cell-intrinsic antiviral activity and the activation of adaptive immunity. HIV-1 infection of DCs triggers an IRF3-dependent innate immune response, which requires the activity of cyclic GAMP synthase (cGAS). We report the results of a targeted RNAi screen utilizing primary human monocyte-derived DCs (MDDCs) to identify immune regulators that directly interface with HIV-1-encoded features to initiate this innate response. Polyglutamine binding protein 1 (PQBP1) emerged as a strong candidate through this analysis. We found that PQBP1 directly binds to reverse-transcribed HIV-1 DNA and interacts with cGAS to initiate an IRF3-dependent innate response. MDDCs derived from Renpenning syndrome patients, who harbor mutations in the PQBP1 locus, possess a severely attenuated innate immune response to HIV-1 challenge, underscoring the role of PQBP1 as a proximal innate sensor of a HIV-1 infection.

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