Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle–Wells syndrome

HM Hoffman, JL Mueller, DH Broide, AA Wanderer… - Nature …, 2001 - nature.com
HM Hoffman, JL Mueller, DH Broide, AA Wanderer, RD Kolodner
Nature genetics, 2001nature.com
Familial cold autoinflammatory syndrome (FCAS, MIM 120100), commonly known as familial
cold urticaria (FCU), is an autosomal-dominant systemic inflammatory disease characterized
by intermittent episodes of rash, arthralgia, fever and conjunctivitis after generalized
exposure to cold 1, 2, 3, 4. FCAS was previously mapped to a 10-cM region on chromosome
1q44 (refs. 5, 6). Muckle–Wells syndrome (MWS; MIM 191900), which also maps to
chromosome 1q44, is an autosomal-dominant periodic fever syndrome with a similar …
Abstract
Familial cold autoinflammatory syndrome (FCAS, MIM 120100), commonly known as familial cold urticaria (FCU), is an autosomal-dominant systemic inflammatory disease characterized by intermittent episodes of rash, arthralgia, fever and conjunctivitis after generalized exposure to cold 1, 2, 3, 4. FCAS was previously mapped to a 10-cM region on chromosome 1q44 (refs. 5, 6). Muckle–Wells syndrome (MWS; MIM 191900), which also maps to chromosome 1q44, is an autosomal-dominant periodic fever syndrome with a similar phenotype except that symptoms are not precipitated by cold exposure and that sensorineural hearing loss is frequently also present 6, 7, 8. To identify the genes for FCAS and MWS, we screened exons in the 1q44 region for mutations by direct sequencing of genomic DNA from affected individuals and controls. This resulted in the identification of four distinct mutations in a gene that segregated with the disorder in three families with FCAS and one family with MWS. This gene, called CIAS1, is expressed in peripheral blood leukocytes and encodes a protein with a pyrin domain 9, 10, 11, a nucleotide-binding site (NBS, NACHT subfamily 12) domain and a leucine-rich repeat (LRR) motif region 13, suggesting a role in the regulation of inflammation and apoptosis.
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