Journal article

Molecular basis of glutathione reductase deficiency in human blood cells


Authors listKamerbeek, NM; van Zwieten, R; de Boer, M; Morren, G; Vuil, H; Bannink, N; Lincke, C; Dolman, KM; Becker, K; Schirmer, RH; Gromer, S; Roos, D

Publication year2007

Pages3560-3566

JournalBlood

Volume number109

Issue number8

ISSN0006-4971

eISSN1528-0020

DOI Linkhttps://doi.org/10.1182/blood-2006-08-042531

PublisherAmerican Society of Hematology (ASH Publications)


Abstract
Hereditary glutathione reductase (GR) deficiency was found in only 2 cases when testing more than 15 000 blood samples. We have investigated the blood cells of 2 patients (1a and 1b) in a previously described family suffering from favism and cataract and of a novel patient (2) presenting with severe neonatal jaundice. Red blood cells and leukocytes of the patients in family 1 did not contain any GR activity, and the GR protein was undetectable by Western blotting. Owing to a 2246-bp deletion in the patients' DNA, translated GR is expected to lack almost the complete dimerization domain, which results in unstable and inactive enzyme. The red blood cells from patient 2 did not exhibit GR activity either, but the patient's leukocytes contained some residual activity that correlated with a weak protein expression. Patient 2 was found to be a compound heterozygote, with a premature stop codon on one allele and a substitution of glycine 330, a highly conserved residue in the superfamily of NAD(P)H-dependent disulfide reductases, into alanine on the other allele. Studies on recombinant GR G330A revealed a drastically impaired thermostability of the protein. This is the first identification of mutations in the GR gene causing clinical GR deficiency.



Citation Styles

Harvard Citation styleKamerbeek, N., van Zwieten, R., de Boer, M., Morren, G., Vuil, H., Bannink, N., et al. (2007) Molecular basis of glutathione reductase deficiency in human blood cells, Blood, 109(8), pp. 3560-3566. https://doi.org/10.1182/blood-2006-08-042531

APA Citation styleKamerbeek, N., van Zwieten, R., de Boer, M., Morren, G., Vuil, H., Bannink, N., Lincke, C., Dolman, K., Becker, K., Schirmer, R., Gromer, S., & Roos, D. (2007). Molecular basis of glutathione reductase deficiency in human blood cells. Blood. 109(8), 3560-3566. https://doi.org/10.1182/blood-2006-08-042531


Last updated on 2025-21-05 at 15:53