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Scientific article
English

Positional cloning of the APECED gene

Published inNature genetics, vol. 17, no. 4, p. 393-398
Publication date1997
Abstract

Autoimmune polyglandular syndrome type I (APS 1, also called APECED) is an autosomal-recessive disorder that maps to human chromosome 21q22.3 between markers D21S49 and D21S171 by linkage studies. We have isolated a novel gene from this region, AIRE (autoimmune regulator), which encodes a protein containing motifs suggestive of a transcription factor including two zinc-finger (PHD-finger) motifs, a proline-rich region and three LXXLL motifs. Two mutations, a C-->T substitution that changes the Arg 257 (CGA) to a stop codon (TGA) and an A-->G substitution that changes the Lys 83 (AAG) to a Glu codon (GAG), were found in this novel gene in Swiss and Finnish APECED patients. The Arg257stop (R257X) is the predominant mutation in Finnish APECED patients, accounting for 10/12 alleles studied. These results indicate that this gene is responsible for the pathogenesis of APECED. The identification of the gene defective in APECED should facilitate the genetic diagnosis and potential treatment of the disease and further enhance our general understanding of the mechanisms underlying autoimmune diseases.

Keywords
  • Amino Acid Sequence
  • Chromosomes, Human, Pair 21
  • Cloning, Molecular/ methods
  • DNA Mutational Analysis
  • Haplotypes
  • Humans
  • Molecular Sequence Data
  • Organ Specificity/genetics
  • Polyendocrinopathies, Autoimmune/ genetics
  • RNA, Messenger/biosynthesis
  • Transcription Factors/biosynthesis/chemistry/ genetics
  • Zinc Fingers/genetics
Citation (ISO format)
NAGAMINE, K. et al. Positional cloning of the APECED gene. In: Nature genetics, 1997, vol. 17, n° 4, p. 393–398. doi: 10.1038/ng1297-393
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ISSN of the journal1061-4036
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