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Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production
Anja Brehm, … , Ivona Aksentijevich, Raphaela Goldbach-Mansky
Anja Brehm, … , Ivona Aksentijevich, Raphaela Goldbach-Mansky
Published October 20, 2015
Citation Information: J Clin Invest. 2015;125(11):4196-4211. https://doi.org/10.1172/JCI81260.
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Research Article Immunology

Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production

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Abstract

Autosomal recessive mutations in proteasome subunit β 8 (PSMB8), which encodes the inducible proteasome subunit β5i, cause the immune-dysregulatory disease chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE), which is classified as a proteasome-associated autoinflammatory syndrome (PRAAS). Here, we identified 8 mutations in 4 proteasome genes, PSMA3 (encodes α7), PSMB4 (encodes β7), PSMB9 (encodes β1i), and proteasome maturation protein (POMP), that have not been previously associated with disease and 1 mutation in PSMB8 that has not been previously reported. One patient was compound heterozygous for PSMB4 mutations, 6 patients from 4 families were heterozygous for a missense mutation in 1 inducible proteasome subunit and a mutation in a constitutive proteasome subunit, and 1 patient was heterozygous for a POMP mutation, thus establishing a digenic and autosomal dominant inheritance pattern of PRAAS. Function evaluation revealed that these mutations variably affect transcription, protein expression, protein folding, proteasome assembly, and, ultimately, proteasome activity. Moreover, defects in proteasome formation and function were recapitulated by siRNA-mediated knockdown of the respective subunits in primary fibroblasts from healthy individuals. Patient-isolated hematopoietic and nonhematopoietic cells exhibited a strong IFN gene-expression signature, irrespective of genotype. Additionally, chemical proteasome inhibition or progressive depletion of proteasome subunit gene transcription with siRNA induced transcription of type I IFN genes in healthy control cells. Our results provide further insight into CANDLE genetics and link global proteasome dysfunction to increased type I IFN production.

Authors

Anja Brehm, Yin Liu, Afzal Sheikh, Bernadette Marrero, Ebun Omoyinmi, Qing Zhou, Gina Montealegre, Angelique Biancotto, Adam Reinhardt, Adriana Almeida de Jesus, Martin Pelletier, Wanxia L. Tsai, Elaine F. Remmers, Lela Kardava, Suvimol Hill, Hanna Kim, Helen J. Lachmann, Andre Megarbane, Jae Jin Chae, Jilian Brady, Rhina D. Castillo, Diane Brown, Angel Vera Casano, Ling Gao, Dawn Chapelle, Yan Huang, Deborah Stone, Yongqing Chen, Franziska Sotzny, Chyi-Chia Richard Lee, Daniel L. Kastner, Antonio Torrelo, Abraham Zlotogorski, Susan Moir, Massimo Gadina, Phil McCoy, Robert Wesley, Kristina I. Rother, Peter W. Hildebrand, Paul Brogan, Elke Krüger, Ivona Aksentijevich, Raphaela Goldbach-Mansky

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Figure 5

Ubiquitin aggregation and proteasome profile changes in CANDLE/PRAAS patient cells.

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Ubiquitin aggregation and proteasome profile changes in CANDLE/PRAAS pat...
(A) Sections from lesional skin biopsies from 2 PRAAS patients, a patient with psoriasis, and a nonlesional skin biopsy from a healthy control were stained with anti-ubiquitin antibody (Dako) for accumulation of polyubiquitinated proteins (brown staining). Scale bar: 50 μm. Representative results from n = 3. (B) Insoluble fractions of RIPA cell lysates of keratinocytes were solubilized in urea lysis buffer and separated on an SDS gel followed by immunoblotting for ubiquitin. Patients show a much stronger accumulation of ubiquitinated proteins in this fraction. Representative results are from n = 2. (C and D) Keratinocytes from healthy controls and CANDLE/PRAAS patients were lysed under native conditions and separated on a native gel. PSMB8 C1 denotes a CANDLE patient homozygous for PSMB8 mutation (T75M/T75M). The lanes for patient 2, PSMB8 C1, and HC1 were run on the same gel, but were noncontiguous. n = 1. (C) Immunoblotting was performed for α6 and β5i. Patient samples harboring β7 and/or β1i mutations were also immunoblotted for β7 and β1i. Asterisk indicates unspecific crossreaction of β1i antibody (Abcam). (D) An in-gel overlay experiment was performed for chymotryptic-like activity to visualize the activity of the proteasome. (E) Plate reader activity assay was measured from whole keratinocyte cell lysates. Patients show a strong reduction in 2 or 3 protease activities. Each of the 5 patients’ and 3 parents’ samples were normalized against HC1+2. Means were estimated from the triplicate values on the normal controls (n = 2). Data were analyzed by restricted maximum likelihood mixed models methods, using the xtmixed procedure in Release 12 of the software package Stata (StataCorp). Data represent the mean ± SD from technical triplicates. n = 1. *P < 0.05; **P < 0.01; ***P < 0.001.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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