Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency

Nat Genet. 2012 May 27;44(7):740-2. doi: 10.1038/ng.2299.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Cortex Neoplasms / genetics
  • Adrenal Cortex Neoplasms / metabolism
  • Adrenal Glands / metabolism
  • Adrenal Insufficiency / enzymology
  • Adrenal Insufficiency / genetics*
  • Adrenal Insufficiency / metabolism
  • Amino Acid Sequence
  • Animals
  • Antioxidants / metabolism
  • Apoptosis / genetics
  • Cell Line, Tumor
  • Child, Preschool
  • Esophageal Achalasia / enzymology
  • Esophageal Achalasia / genetics*
  • Esophageal Achalasia / metabolism
  • Exome
  • Glucocorticoids / genetics
  • Glucocorticoids / metabolism
  • Humans
  • Infant
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria / genetics
  • Molecular Sequence Data
  • Mutation*
  • NADP Transhydrogenases / genetics*
  • Oxidation-Reduction
  • Reactive Oxygen Species / metabolism
  • Sequence Alignment

Substances

  • Antioxidants
  • Glucocorticoids
  • Reactive Oxygen Species
  • NADP Transhydrogenases

Supplementary concepts

  • Achalasia Addisonianism Alacrimia syndrome