Structural, expression, and evolutionary analysis of mouse CIASI

被引:48
作者
Anderson, JP
Mueller, JL
Rosengren, S
Boyle, DL
Schaner, P
Cannon, SB
Goodyear, CS
Hoffman, HM
机构
[1] Univ Calif San Diego, UCSD Div Rheumatol Allergy & Immunol, Sch Med, Rheumat Dis Core Ctr, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Pediat, Sch Med, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Ludwig Inst Canc Res, Sch Med, La Jolla, CA 92093 USA
[4] Univ Michigan, Dept Cell & Dev Biol, Ann Arbor, MI 48109 USA
[5] Univ Minnesota, Dept Plant Pathol, St Paul, MN 55108 USA
关键词
cryopyrin; pyrin; primate; NACHT; autoinflammatory; NALP;
D O I
10.1016/j.gene.2004.05.002
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mutations in the human CIAS1 (hCIAS1) gene have been identified in a continuum of inflammatory disorders including familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), and neonatal onset multisystem inflammatory disease (NOMID). CIAS1 codes for the protein Cryopyrin, which appears to play a role in innate immune function by regulating the production of proinflammatory cytokines. Human and mouse Cryopyrin are highly conserved and consist of three functional domains including a pyrin domain, an NACHT domain, and a leucine-rich repeat (LRR) domain that are characteristics of the NALP family of proteins. The pyrin and NACHT domains of Cryopyrin and other NALP proteins are highly conserved among primate and nonprimate mammals, suggesting purifying selection throughout mammalian evolution. Cryopyrin expression is also very similar in human and mouse with mouse CIAS1 mRNA expression found primarily in peripheral blood leukocytes consistent with the postulated inflammatory function. We also detected significant expression in mouse eye and skin tissue, which is consistent with symptoms observed in human Cryopyrin-associated diseases. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:25 / 34
页数:10
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