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Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease

Tom Le Voyer 1 Anna-Lena Neehus 1 Rui Yang 2 Masato Ogishi 2 Jérémie Rosain Fayhan Alroqi 3, 4 Maha Alshalan 3 Sophie Blumental 5 Fatima Al Ali 6 Taushif Khan 6 Manar Ata 6 Laurence Rozen 7 Anne Demulder 7 Paul Bastard Conor Gruber 8 Manon Roynard Yoann Seeleuthener Franck Rapaport 2 Benedetta Bigio 2 Maya Chrabieh Danielle Sng 9 Laureline Berteloot 10 Nathalie Boddaert 10 Flore Rozenberg 11 Saleh Al-Muhsen 12 Aida Bertoli-Avella 13 Laurent Abel 2 Dusan Bogunovic 7, 8 Nico Marr 6, 14 Davood Mansouri 15 Fuad Al Mutairi 4, 3 Vivien Béziat 2 Dominique Weil 16, 17 Seyed Alireza Mahdaviani 15 Alina Ferster 5 Shen-Ying Zhang 2 Bruno Reversade 9 Stéphanie Boisson-Dupuis 2 Jean-Laurent Casanova 2, 18 Jacinta Bustamante 2, 10 
Abstract : Human inborn errors of IFN-γ underlie mycobacterial disease, due to insufficient IFN-γ production by lymphoid cells, impaired myeloid cell responses to this cytokine, or both. We report four patients from two unrelated kindreds with intermittent monocytosis and mycobacterial disease, including bacillus Calmette–Guérin-osis and disseminated tuberculosis, and without any known inborn error of IFN-γ. The patients are homozygous for ZNFX1 variants (p.S959* and p.E1606Rfs*10) predicted to be loss of function (pLOF). There are no subjects homozygous for pLOF variants in public databases. ZNFX1 is a conserved and broadly expressed helicase, but its biology remains largely unknown. It is thought to act as a viral double-stranded RNA sensor in mice, but these patients do not suffer from severe viral illnesses. We analyze its subcellular localization upon overexpression in A549 and HeLa cell lines and upon stimulation of THP1 and fibroblastic cell lines. We find that this cytoplasmic protein can be recruited to or even induce stress granules. The endogenous ZNFX1 protein in cell lines of the patient homozygous for the p.E1606Rfs*10 variant is truncated, whereas ZNFX1 expression is abolished in cell lines from the patients with the p.S959* variant. Lymphocyte subsets are present at normal frequencies in these patients and produce IFN-γ normally. The hematopoietic and nonhematopoietic cells of the patients tested respond normally to IFN-γ. Our results indicate that human ZNFX1 is associated with stress granules and essential for both monocyte homeostasis and protective immunity to mycobacteria.
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https://hal.archives-ouvertes.fr/hal-03371686
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Submitted on : Tuesday, October 12, 2021 - 3:35:24 PM
Last modification on : Thursday, October 20, 2022 - 3:10:07 PM
Long-term archiving on: : Thursday, January 13, 2022 - 6:05:17 PM

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Tom Le Voyer, Anna-Lena Neehus, Rui Yang, Masato Ogishi, Jérémie Rosain, et al.. Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease. Proceedings of the National Academy of Sciences of the United States of America, 2021, 118 (15), pp.e2102804118. ⟨10.1073/pnas.2102804118⟩. ⟨hal-03371686⟩

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