Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency

Adrian Clark and colleagues report mutations in the NNT gene encoding nicotinamide nucleotide transhydrogenase in familial glucocorticoid deficiency (FGD). Using targeted exome sequencing, we identified mutations in NNT , an antioxidant defense gene, in individuals with familial glucocorticoid defic...

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Veröffentlicht in:Nature genetics 2012-07, Vol.44 (7), p.740-742
Hauptverfasser: Meimaridou, Eirini, Kowalczyk, Julia, Guasti, Leonardo, Hughes, Claire R, Wagner, Florian, Frommolt, Peter, Nürnberg, Peter, Mann, Nicholas P, Banerjee, Ritwik, Saka, H Nurcin, Chapple, J Paul, King, Peter J, Clark, Adrian J L, Metherell, Louise A
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Sprache:eng
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Zusammenfassung:Adrian Clark and colleagues report mutations in the NNT gene encoding nicotinamide nucleotide transhydrogenase in familial glucocorticoid deficiency (FGD). Using targeted exome sequencing, we identified mutations in NNT , an antioxidant defense gene, in individuals with familial glucocorticoid deficiency. In mice with Nnt loss, higher levels of adrenocortical cell apoptosis and impaired glucocorticoid production were observed. NNT knockdown in a human adrenocortical cell line resulted in impaired redox potential and increased reactive oxygen species (ROS) levels. Our results suggest that NNT may have a role in ROS detoxification in human adrenal glands.
ISSN:1061-4036
1546-1718
DOI:10.1038/ng.2299