Emerging role of long noncoding RNAs as regulators of innate immune cell development and inflammatory gene expression
Program in Innate Immunity; Division of Infectious Diseases and Immunology, Department of Medicine
The innate immune system represents the first line of defense during infection and is initiated by the detection of conserved microbial products by germline-encoded pattern recognition receptors (PRRs). Sensing through PRRs induces broad transcriptional changes that elicit powerful inflammatory responses. Tight regulation of these processes depends on multiple regulatory checkpoints, including noncoding RNA species such as microRNAs. In addition, long noncoding RNAs (lncRNAs) have recently gained attention as important regulators of gene expression acting through versatile interactions with DNA, RNA, or proteins. As such, these RNAs have a multitude of mechanisms to modulate gene expression. Here, we summarize recent advances in this rapidly moving and evolving field. We highlight the contribution of lncRNAs to both the development and activation of innate immune cells, whether it is in the nucleus, where lncRNAs alter the transcription of target genes through interaction with transcription factors, chromatin-modifying complexes or heterogeneous ribonucleoprotein complexes, or in the cytosol where they can control the stability of target mRNAs. In addition, we discuss experimental approaches required to comprehensively investigate the function of a candidate noncoding RNA locus, including loss-of-function approaches encompassing genomic deletions, RNA interference, locked nucleic acids, and various adaptions of the CRISPR/Cas9 technology.
Rights and Permissions
Citation: Eur J Immunol. 2016 Mar;46(3):504-12. doi: 10.1002/eji.201444558. Epub 2016 Feb 24. Link to article on publisher's site
Gene expression, Immune regulation, Inflammation, Innate immunity, (Long) noncoding RNA
European journal of immunology
Elling, Roland; Chan, Jennie; and Fitzgerald, Katherine A., "Emerging role of long noncoding RNAs as regulators of innate immune cell development and inflammatory gene expression" (2016). University of Massachusetts Medical School Faculty Publications. 1155.