GSBS Student Publications
Title
The long noncoding RNA THRIL regulates TNFalpha expression through its interaction with hnRNPL
GSBS Program
Biochemistry & Molecular Pharmacology
UMMS Affiliation
Department of Biochemistry and Molecular Pharmacology, Chemical Biology Program
Date
1-21-2014
Document Type
Article
Medical Subject Headings
Cell Line; Cell Nucleolus; Cytokines; Enzyme-Linked Immunosorbent Assay; Gene Expression Profiling; *Gene Expression Regulation; Heterogeneous-Nuclear Ribonucleoprotein L; Humans; Immunity, Innate; Inflammation; Interleukin-6; Macrophages; Mucocutaneous Lymph Node Syndrome; Oligonucleotide Array Sequence Analysis; RNA, Long Noncoding; Tumor Necrosis Factor-alpha
Disciplines
Cell Biology | Genetics and Genomics | Immunity | Immunology and Infectious Disease
Abstract
Thousands of large intergenic noncoding RNAs (lincRNAs) have been identified in the mammalian genome, many of which have important roles in regulating a variety of biological processes. Here, we used a custom microarray to identify lincRNAs associated with activation of the innate immune response. A panel of 159 lincRNAs was found to be differentially expressed following innate activation of THP1 macrophages. Among them, linc1992 was shown to be expressed in many human tissues and was required for induction of TNFalpha expression. Linc1992 bound specifically to heterogenous nuclear ribonucleoprotein L (hnRNPL) and formed a functional linc1992-hnRNPL complex that regulated transcription of the TNFalpha gene by binding to its promoter. Transcriptome analysis revealed that linc1992 was required for expression of many immune-response genes, including other cytokines and transcriptional and posttranscriptional regulators of TNFalpha expression, and that knockdown of linc1992 caused dysregulation of these genes during innate activation of THP1 macrophages. Therefore, we named linc1992 THRIL (TNFalpha and hnRNPL related immunoregulatory LincRNA). Finally, THRIL expression was correlated with the severity of symptoms in patients with Kawasaki disease, an acute inflammatory disease of childhood. Collectively, our data provide evidence that lincRNAs and their binding proteins can regulate TNFalpha expression and may play important roles in the innate immune response and inflammatory diseases in humans.
Rights and Permissions
Citation: Proc Natl Acad Sci U S A. 2014 Jan 21;111(3):1002-7. doi: 10.1073/pnas.1313768111. Epub 2013 Dec 26. Link to article on publisher's site
DOI of Published Version
10.1073/pnas.1313768111
Related Resources
Keywords
innate immunity, inflammation, Toll-like receptors
Journal Title
Proceedings of the National Academy of Sciences of the United States of America
PubMed ID
24371310
Repository Citation
Li, Zhonghan; Chao, Ti-Chun; Chang, Kung-Yen; Lin, Nianwei; Patil, Veena S.; Shimizu, Chisato; Head, Steven R.; Burns, Jane C.; and Rana, Tariq M., "The long noncoding RNA THRIL regulates TNFalpha expression through its interaction with hnRNPL" (2014). GSBS Student Publications. 1945.
https://escholarship.umassmed.edu/gsbs_sp/1945
Comments
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