| Literature DB >> 22730530 |
Shunichiro Takezaki1, Masafumi Yamada, Masahiko Kato, Myoung-Ja Park, Kenichi Maruyama, Yasuhiro Yamazaki, Natsuko Chida, Osamu Ohara, Ichiro Kobayashi, Tadashi Ariga.
Abstract
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.Entities:
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Year: 2012 PMID: 22730530 DOI: 10.4049/jimmunol.1200926
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422