Identification of the secretory leukocyte protease inhibitor (SLPI) as a target of IRF-1 regulation

被引:0
|
作者
Hannah Nguyen
Lindsay Teskey
Rongtuan Lin
John Hiscott
机构
[1] Terry Fox Molecular Oncology Group,Department of Microbiology and Immunology
[2] Lady Davis Institute for Medical Research,Department of Medicine
[3] Sir Mortimer B Davis Jewish General Hospital,undefined
[4] McGill University,undefined
[5] Montreal,undefined
[6] McGill University,undefined
[7] Montreal,undefined
[8] McGill University,undefined
[9] Montreal,undefined
来源
Oncogene | 1999年 / 18卷
关键词
interferon regulatory factor (IRF)-1; secretory leukocyte protease inhibitor (SLPI); transcription;
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学科分类号
摘要
Interferon Regulatory Factor (IRF)-1 is a multifunctional transcription factor, involved in cell growth regulation, pathogen response and immune activation. To identify novel gene targets that may contribute to IRF-1 mediated activities, RNA fingerprinting was performed using NIH3T3 cells that inducibly express a hybrid form of IRF-1 under tetracycline regulated control. Secretory leukocyte protease inhibitor (SLPI) – a regulator of inflammation and an inhibitor of the LPS response – was identified as a gene repressed after doxycycline induced IRF-1 expression. Preliminary analysis of the human SLPI promoter identified an ISRE-like site located within the −221 to −200 region to which IRF-1 binds and a second, putative IRF-1 binding site upstream of the TATA box. Furthermore, co-transfection studies demonstrated that SLPI expression was inhibited by IRF-1 co-expression. The identification of SLPI as a target of IRF-1 regulation reveals a unique involvement of IRF-1 in repression of gene transcription and assigns a novel role for IRF-1 in inflammation.
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页码:5455 / 5463
页数:8
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