We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
A new CARD15 mutation in Blau syndrome.
- Authors
van Duist, Marjan M; Albrecht, Mario; Podswiadek, Marta; Giachino, Daniela; Lengauer, Thomas; Punzi, Leonardo; De Marchi, Mario
- Abstract
The caspase recruitment domain gene CARD15/NOD2, encoding a cellular receptor involved in an NF-?B-mediated pathway of innate immunity, was first identified as a major susceptibility gene for Crohn's disease (CD), and more recently, as responsible for Blau syndrome (BS), a rare autosomal-dominant trait characterized by arthritis, uveitis, skin rash and granulomatous inflammation. While CARD15 variants associated with CD are located within or near the C-terminal leucine-rich repeat domain and cause decreased NF-?B activation, BS mutations affect the central nucleotide-binding NACHT domain and result in increased NF-?B activation. In an Italian family with BS, we detected a novel mutation E383K, whose pathogenicity is strongly supported by cosegregation with the disease in the family and absence in controls, and by the evolutionary conservation and structural role of the affected glutamate close to the Walker B motif of the nucleotide-binding site in the NACHT domain. Interestingly, substitutions at corresponding positions in another NACHT family member cause similar autoinflammatory phenotypes.European Journal of Human Genetics (2005) 13, 742-747. doi:10.1038/sj.ejhg.5201404 Published online 6 April 2005
- Subjects
NATURAL immunity; JOINT diseases; EYE inflammation; UVEITIS; AMINO acids; HUMAN genetics
- Publication
European Journal of Human Genetics, 2005, Vol 13, Issue 6, p742
- ISSN
1018-4813
- Publication type
Article
- DOI
10.1038/sj.ejhg.5201404