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Identification of eight novel proteasome variants in five unrelated cases of proteasome-associated autoinflammatory syndromes (PRAAS).

Authors :
Papendorf JJ
Ebstein F
Alehashemi S
Piotto DGP
Kozlova A
Terreri MT
Shcherbina A
Rastegar A
Rodrigues M
Pereira R
Park S
Lin B
Uss K
Möller S
da Silva Pina AF
Sztajnbok F
Torreggiani S
Niemela J
Stoddard J
Rosenzweig SD
Oler AJ
McNinch C
de Guzman MM
Fonseca A
Micheloni N
Fraga MM
Perazzio SF
Goldbach-Mansky R
de Jesus AA
Krüger E
Source :
Frontiers in immunology [Front Immunol] 2023 Aug 04; Vol. 14, pp. 1190104. Date of Electronic Publication: 2023 Aug 04 (Print Publication: 2023).
Publication Year :
2023

Abstract

Mutations in genes coding for proteasome subunits and/or proteasome assembly helpers typically cause recurring autoinflammation referred to as chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperatures (CANDLE) or proteasome-associated autoinflammatory syndrome (PRAAS). Patients with CANDLE/PRAAS present with mostly chronically elevated type I interferon scores that emerge as a consequence of increased proteotoxic stress by mechanisms that are not fully understood. Here, we report on five unrelated patients with CANDLE/PRAAS carrying novel inherited proteasome missense and/or nonsense variants. Four patients were compound heterozygous for novel pathogenic variants in the known CANDLE/PRAAS associated genes, PSMB8 and PSMB10 , whereas one patient showed additive loss-of-function mutations in PSMB8 . Variants in two previously not associated proteasome genes, PSMA5 and PSMC5 , were found in a patient who also carried the PSMB8 founder mutation, p.T75M. All newly identified mutations substantially impact the steady-state expression of the affected proteasome subunits and/or their incorporation into mature 26S proteasomes. Our observations expand the spectrum of PRAAS-associated genetic variants and improve a molecular diagnosis and genetic counseling of patients with sterile autoinflammation.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The reviewer SD declared a past co-authorship with the authors FE and EK to the handling editor.<br /> (Copyright © 2023 Papendorf, Ebstein, Alehashemi, Piotto, Kozlova, Terreri, Shcherbina, Rastegar, Rodrigues, Pereira, Park, Lin, Uss, Möller, da Silva Pina, Sztajnbok, Torreggiani, Niemela, Stoddard, Rosenzweig, Oler, McNinch, de Guzman, Fonseca, Micheloni, Fraga, Perazzio, Goldbach-Mansky, de Jesus and Krüger.)

Details

Language :
English
ISSN :
1664-3224
Volume :
14
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
37600812
Full Text :
https://doi.org/10.3389/fimmu.2023.1190104