| Literature DB >> 10192386 |
E Jouanguy1, S Lamhamedi-Cherradi, D Lammas, S E Dorman, M C Fondanèche, S Dupuis, R Döffinger, F Altare, J Girdlestone, J F Emile, H Ducoulombier, D Edgar, J Clarke, V A Oxelius, M Brai, V Novelli, K Heyne, A Fischer, S M Holland, D S Kumararatne, R D Schreiber, J L Casanova.
Abstract
The immunogenetic basis of severe infections caused by bacille Calmette-Guérin vaccine and environmental mycobacteria in humans remains largely unknown. We describe 18 patients from several generations of 12 unrelated families who were heterozygous for 1 to 5 overlapping IFNGR1 frameshift small deletions and a wild-type IFNGR1 allele. There were 12 independent mutation events at a single mutation site, defining a small deletion hotspot. Neighbouring sequence analysis favours a small deletion model of slipped mispairing events during replication. The mutant alleles encode cell-surface IFNgamma receptors that lack the intra-cytoplasmic domain, which, through a combination of impaired recycling, abrogated signalling and normal binding to IFNgamma exert a dominant-negative effect. We thus report a hotspot for human IFNGR1 small deletions that confer dominant susceptibility to infections caused by poorly virulent mycobacteria.Entities:
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Year: 1999 PMID: 10192386 DOI: 10.1038/7701
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330