Long noncoding RNA IL6-AS1 is highly expressed in chronic obstructive pulmonary disease and is associated with interleukin 6 by targeting miR-149-5p and early B-cell factor 1

Clin Transl Med. 2021 Jul;11(7):e479. doi: 10.1002/ctm2.479.

Abstract

Chronic obstructive pulmonary disease is a complex condition with multiple etiologies, including inflammation. We identified a novel long noncoding RNA (lncRNA), interleukin 6 antisense RNA 1 (IL6-AS1), which is upregulated in this disease and is associated with airway inflammation. We found that IL6-AS1 promotes the expression of inflammatory factors, especially interleukin (IL) 6. Mechanistically, cytoplasmic IL6-AS1 acts as an endogenous sponge by competitively binding to the microRNA miR-149-5p to stabilize IL-6 mRNA. Nuclear IL6-AS1 promotes IL-6 transcription by recruiting early B-cell factor 1 to the IL-6 promoter, which increases the methylation of the H3K4 histone and acetylation of the H3K27 histone. We propose a model of lncRNA expression in both the nucleus and cytoplasm that exerts similar effects through differing mechanisms, and IL6-AS1 probably increases inflammation via multiple pathways.

Keywords: IL-6; IL6-AS1; chronic obstructive pulmonary disease; early B-cell factor 1; hsa-miR-149-5p; inflammation; long noncoding RNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antagomirs / metabolism
  • Cytokines / metabolism
  • Cytoplasm / metabolism
  • Fibroblasts / cytology
  • Fibroblasts / metabolism
  • Histones / metabolism
  • Humans
  • Interleukin-6 / chemistry
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism*
  • Methylation
  • MicroRNAs / antagonists & inhibitors
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Promoter Regions, Genetic
  • Protein Binding
  • Pulmonary Disease, Chronic Obstructive / genetics
  • Pulmonary Disease, Chronic Obstructive / pathology*
  • RNA Interference
  • RNA, Long Noncoding / antagonists & inhibitors
  • RNA, Long Noncoding / genetics
  • RNA, Long Noncoding / metabolism*
  • RNA, Small Interfering / metabolism
  • Trans-Activators / chemistry
  • Trans-Activators / metabolism*

Substances

  • Antagomirs
  • Cytokines
  • EBF1 protein, human
  • Histones
  • Interleukin-6
  • MIRN149 microRNA, human
  • MicroRNAs
  • RNA, Long Noncoding
  • RNA, Small Interfering
  • Trans-Activators