A Long Noncoding RNA Mediates Both Activation and Repression of Immune Response Genes

Author:

Carpenter Susan12,Aiello Daniel1,Atianand Maninjay K.1,Ricci Emiliano P.3,Gandhi Pallavi1,Hall Lisa L.4,Byron Meg4,Monks Brian1,Henry-Bezy Meabh1,Lawrence Jeanne B.4,O’Neill Luke A. J.2,Moore Melissa J.3,Caffrey Daniel R.1,Fitzgerald Katherine A.1

Affiliation:

1. Division of Infectious Diseases and Immunology, Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01605, USA.

2. School of Biochemistry and Immunology, Trinity College Dublin, Dublin 2, Ireland.

3. Howard Hughes Medical Institute, University of Massachusetts Medical School, Worcester, MA 01605, USA.

4. Department of Cell and Developmental Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.

Abstract

A New Linc in Innate Immunity Long noncoding RNAs (lncRNAs) have recently emerged as important regulators of gene expression in a wide variety of biological processes, although specific roles for these molecules in the immune system have not been described. Carpenter et al. (p. 789 , published online 1 August) now define the function of one such lncRNA in the immune system, lincRNA-Cox2. Whole-transcriptome profiling revealed that lincRNA-Cox2 was induced in mouse macrophages in response to activation of Toll-like receptors—molecules that detect microbes and alert the immune system to respond. LincRNA-Cox2 both positively and negatively regulated the expression of distinct groups of inflammatory genes. Negative regulation of gene expression was mediated by lincRNA-Cox interaction with heterogeneous nuclear ribonucleoprotein A/B and A2/B1.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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