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Chronic Mucocutaneous Candidiasis Caused by a Gain-of-Function Mutation in the STAT1 DNA-Binding Domain
Author(s) -
Shunichiro Takezaki,
Masafumi Yamada,
Masahiko Katô,
Hyuntae Park,
Kenichi Maruyama,
Yasuhiro Yamazaki,
Natsuko Chida,
Osamu Ohara,
Ichiro Kobayashi,
Tadashi Ariga
Publication year - 2012
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1200926
Subject(s) - chronic mucocutaneous candidiasis , dephosphorylation , mutation , dna , biology , dna binding domain , phosphorylation , mutagenesis , stat1 , binding domain , primary immunodeficiency , exon , genetics , medicine , gene , binding site , transcription factor , immune system , disease , phosphatase
Chronic mucocutaneous candidiasis (CMC) is a heterogeneous group of primary immunodeficiency diseases characterized by chronic and recurrent Candida infections of the skin, nails, and oropharynx. Gain-of-function mutations in STAT1 were very recently shown to be responsible for autosomal-dominant or sporadic cases of CMC. The reported mutations have been exclusively localized in the coiled-coil domain, resulting in impaired dephosphorylation of STAT1. However, recent crystallographic analysis and direct mutagenesis experiments indicate that mutations affecting the DNA-binding domain of STAT1 could also lead to persistent phosphorylation of STAT1. To our knowledge, this study shows for the first time that a DNA-binding domain mutation of c.1153C>T in exon 14 (p.T385M) is the genetic cause of sporadic CMC in two unrelated Japanese patients. The underlying mechanisms involve a gain of STAT1 function due to impaired dephosphorylation as observed in the coiled-coil domain mutations.

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