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Nature. 2016 Sep 8;537(7619):239-243. doi: 10.1038/nature19346. Epub 2016 Aug 15.

The long non-coding RNA Morrbid regulates Bim and short-lived myeloid cell lifespan.

Author information

1
Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
2
Institute for Immunology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
3
The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut 06032, USA.
4
Department of Genetics and Genomic Sciences, University of Connecticut Health Center, Farmington, Connecticut 06032, USA.
5
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
6
Department of Bioengineering, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
7
Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
8
Howard Hughes Medical Institute, Yale University, New Haven, Connecticut 06510, USA.
9
Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
10
McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, Baltimore, Maryland 21205, USA.
11
Department of Neuroscience, Johns Hopkins University, Baltimore, Maryland 21205, USA.
12
Biological and Biomedical Sciences, Harvard Medical School, Boston, Massachusetts 02115, USA.
13
Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
14
Division of Transplant Immunology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.

Abstract

Neutrophils, eosinophils and 'classical' monocytes collectively account for about 70% of human blood leukocytes and are among the shortest-lived cells in the body. Precise regulation of the lifespan of these myeloid cells is critical to maintain protective immune responses and minimize the deleterious consequences of prolonged inflammation. However, how the lifespan of these cells is strictly controlled remains largely unknown. Here we identify a long non-coding RNA that we termed Morrbid, which tightly controls the survival of neutrophils, eosinophils and classical monocytes in response to pro-survival cytokines in mice. To control the lifespan of these cells, Morrbid regulates the transcription of the neighbouring pro-apoptotic gene, Bcl2l11 (also known as Bim), by promoting the enrichment of the PRC2 complex at the Bcl2l11 promoter to maintain this gene in a poised state. Notably, Morrbid regulates this process in cis, enabling allele-specific control of Bcl2l11 transcription. Thus, in these highly inflammatory cells, changes in Morrbid levels provide a locus-specific regulatory mechanism that allows rapid control of apoptosis in response to extracellular pro-survival signals. As MORRBID is present in humans and dysregulated in individuals with hypereosinophilic syndrome, this long non-coding RNA may represent a potential therapeutic target for inflammatory disorders characterized by aberrant short-lived myeloid cell lifespan.

PMID:
27525555
PMCID:
PMC5161578
DOI:
10.1038/nature19346
[Indexed for MEDLINE]
Free PMC Article
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