Cutting Edge: A Natural Antisense Transcript, AS-IL1α, Controls Inducible Transcription of the Proinflammatory Cytokine IL-1α

被引:90
作者
Chan, Jennie [1 ]
Atianand, Maninjay [1 ]
Jiang, Zhaozhao [1 ]
Carpenter, Susan [1 ,2 ]
Aiello, Daniel [1 ]
Elling, Roland [1 ]
Fitzgerald, Katherine A. [1 ,3 ]
Caffrey, Daniel R. [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Med, Program Innate Immun,Div Infect Dis, Worcester, MA 01605 USA
[2] Univ Calif San Francisco, Dept Immunol & Microbiol, San Francisco, CA 94143 USA
[3] Norwegian Univ Sci & Technol, Dept Canc Res & Mol Med, Ctr Mol Inflammat Res, N-7491 Trondheim, Norway
基金
新加坡国家研究基金会; 美国国家卫生研究院;
关键词
LONG NONCODING RNAS; EXPRESSION; GENES;
D O I
10.4049/jimmunol.1500264
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Natural antisense transcripts (NATs) are a class of long noncoding RNAs (lncRNAs) that are complementary to other protein-coding genes. Although thousands of NATs are encoded by mammalian genomes, their functions in innate immunity are unknown. In this study, we identified and characterized a novel NAT, AS-IL1 alpha, which is partially complementary to IL-1 alpha. Similar to IL-1 alpha, AS-IL1 alpha is expressed at low levels in resting macrophages and is induced following infection with Listeria monocytogenes or stimulation with TLR ligands (Pam(3)CSK(4), LPS, polyinosinic-polycytidylic acid). Inducible expression of IL-1 alpha mRNA and protein were significantly reduced in macrophages expressing shRNA that target AS-IL1 alpha. AS-IL1 alpha is located in the nucleus and did not alter the stability of IL-1 alpha mRNA. Instead, AS-IL1 alpha was required for the recruitment of RNA polymerase II to the IL-1 alpha promoter. In summary, our studies identify AS-IL1 alpha as an important regulator of IL-1 alpha transcription during the innate immune response.
引用
收藏
页码:1359 / 1363
页数:5
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