Two different STAT1 gain-of-function mutations lead to diverse IFN-γ-mediated gene expression

被引:13
|
作者
Ovadia, Adi [1 ,2 ,3 ,4 ]
Sharfe, Nigel [1 ,2 ,3 ,4 ]
Hawkins, Cynthia [5 ]
Laughlin, Suzanne [6 ]
Roifman, Chaim M. [1 ,2 ,3 ,4 ]
机构
[1] Hosp Sick Children, Dept Paediat, Div Immunol & Allergy, Toronto, ON, Canada
[2] Univ Toronto, Toronto, ON, Canada
[3] Hosp Sick Children, Canadian Ctr Primary Immunodeficiency, Toronto, ON, Canada
[4] Hosp Sick Children, Jeffrey Modell Res Lab Diag Primary Immunodeficie, Toronto, ON, Canada
[5] Hosp Sick Children, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[6] Hosp Sick Children, Dept Radiol, Toronto, ON, Canada
来源
NPJ GENOMIC MEDICINE | 2018年 / 3卷
关键词
UNDERLIE;
D O I
10.1038/s41525-018-0063-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Signal transducer and activator of transcription 1 (STAT1) regulates multiple biological processes downstream of a variety of cytokine receptors in many cell types. Heterozygous gain-of-function (GOF) mutations in STAT1 have been associated with a diverse phenotype encompassing chronic mucocutaneous candidiasis (CMCC) and declining immunity. There is no dear correlation between STAT1 domain-specific mutations and phenotype, and it remains unclear why GOF mutations in STAT1 result in such a wide spectrum of clinical presentations. To begin exploring this dilemma, we have studied the patterns of gene expression mediated by two different GOF mutations. Analysis of IFN-gamma response elements using RNA microarrays in cells transfected with the rare H629Y mutant or the common R274G mutant showed distinct patterns of gene expression. We show here that the impact of GOF mutations in STAT1 is variant-specific. This difference in gene expression may explain the diversity in clinical manifestations experienced by these patients.
引用
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页数:5
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