Journal article
Mutations in the selenocysteine insertion sequence-binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans
E Schoenmakers, M Agostini, C Mitchell, N Schoenmakers, L Papp, O Rajanayagam, R Padidela, L Ceron-Gutierrez, R Doffinger, C Prevosto, J Luan, S Montano, J Lu, M Castanet, N Clemons, M Groeneveld, P Castets, M Karbaschi, S Aitken, A Dixon Show all
Journal of Clinical Investigation | Published : 2010
DOI: 10.1172/JCI43653
Abstract
Selenium, a trace element that is fundamental to human health, is incorporated into some proteins as seleno-cysteine (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 ..
View full abstractGrants
Awarded by Medical Research Council
Funding Acknowledgements
This work was supported by the Wellcome Trust and National Institute for Health Research Cambridge Biomedical Research Centre (to K Chatterjee, M Gurnell, and R. Semple), the Medical Research Council (to R. Fitzgerald and N Wareham), and Muscular Dystrophy Campaign Centre (to F Muntoni) We thank Afzal Chaudhry for advice with statistical analysis and Greg Strachan for help with confocal microscopy