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Mutations in the selenocysteine insertion sequence–binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans
Erik Schoenmakers, et al.
Erik Schoenmakers, et al.
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Research Article Genetics

Mutations in the selenocysteine insertion sequence–binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans

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Abstract

Selenium, a trace element that is fundamental to human health, is incorporated into some proteins as selenocysteine (Sec), generating a family of selenoproteins. Sec incorporation is mediated by a multiprotein complex that includes Sec insertion sequence–binding protein 2 (SECISBP2; also known as SBP2). Here, we describe subjects with compound heterozygous defects in the SECISBP2 gene. These individuals have reduced synthesis of most of the 25 known human selenoproteins, resulting in a complex phenotype. Azoospermia, with failure of the latter stages of spermatogenesis, was associated with a lack of testis-enriched selenoproteins. An axial muscular dystrophy was also present, with features similar to myopathies caused by mutations in selenoprotein N (SEPN1). Cutaneous deficiencies of antioxidant selenoenzymes, increased cellular ROS, and susceptibility to ultraviolet radiation–induced oxidative damage may mediate the observed photosensitivity. Reduced levels of selenoproteins in peripheral blood cells were associated with impaired T lymphocyte proliferation, abnormal mononuclear cell cytokine secretion, and telomere shortening. Paradoxically, raised ROS in affected subjects was associated with enhanced systemic and cellular insulin sensitivity, similar to findings in mice lacking the antioxidant selenoenzyme glutathione peroxidase 1 (GPx1). Thus, mutation of SECISBP2 is associated with a multisystem disorder with defective biosynthesis of many selenoproteins, highlighting their role in diverse biological processes.

Authors

Erik Schoenmakers, Maura Agostini, Catherine Mitchell, Nadia Schoenmakers, Laura Papp, Odelia Rajanayagam, Raja Padidela, Lourdes Ceron-Gutierrez, Rainer Doffinger, Claudia Prevosto, Jian’an Luan, Sergio Montano, Jun Lu, Mireille Castanet, Nick Clemons, Matthijs Groeneveld, Perrine Castets, Mahsa Karbaschi, Sri Aitken, Adrian Dixon, Jane Williams, Irene Campi, Margaret Blount, Hannah Burton, Francesco Muntoni, Dominic O’Donovan, Andrew Dean, Anne Warren, Charlotte Brierley, David Baguley, Pascale Guicheney, Rebecca Fitzgerald, Alasdair Coles, Hill Gaston, Pamela Todd, Arne Holmgren, Kum Kum Khanna, Marcus Cooke, Robert Semple, David Halsall, Nicholas Wareham, John Schwabe, Lucia Grasso, Paolo Beck-Peccoz, Arthur Ogunko, Mehul Dattani, Mark Gurnell, Krishna Chatterjee

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Figure 8

Impaired T cell proliferation, with reduced antioxidant defense and telomere shortening, in PBMCs.

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Increased UV sensitivity in dermal fibroblasts.
Untreated or α-tocophero...
(A) Persistently reduced peripheral rbc and lymphocyte counts from P1 over a 36-month period. (B) Impaired T cell proliferation in P1. Following stimulation of PBMCs from P1 and his brother, FACS analysis shows dilution of the intracellular dye (CFSE) in CD3+ T cells. (C) Selenoprotein levels in 75Se-labeled T cells, with 35S-Met labeling of cells confirming comparable protein loading, in P1 and an age- and sex-matched control subject. Arrows denote positions of bands corresponding to specific selenoproteins (TrxR, GPx1, GPx4, and Sep15). (D) TrxR activity in PBMCs from P1 compared with his brother and an age- and sex-matched control subject. (E) ROS production in PBMCs from P1, his mother, and an age- and sex-matched control, determined as described for dermal fibroblasts in Figure 6B. (F) ROS levels in RBCs from P1 (each symbol is an independent determination on a different occasion) or control subjects (each symbol is a measurement from a different individual). (G) Telomeric shortening in PBMCs of P1. Average telomere length (kb) in DNA from PBMCs of P1, his brother (Br), and 3 age- and sex-matched control subjects, determined by Southern blotting using a telomere-specific probe. Mw, molecular weight size marker.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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