Transcriptional control of a novel long noncoding RNA Mymsl in smooth muscle cells by a single Cis-element and its initial functional characterization in vessels

J Mol Cell Cardiol. 2020 Jan:138:147-157. doi: 10.1016/j.yjmcc.2019.11.148. Epub 2019 Nov 18.

Abstract

Differentiated vascular smooth muscle cells (VSMCs) are crucial in maintaining vascular homeostasis. While the coding transcriptome of the differentiated VSMC phenotype has been defined, we know little about its noncoding signature. Herein, we identified a Myocardin-induced muscle specific long noncoding RNA (lncRNA) (Mymsl) downregulated upon VSMC phenotypic modulation. We demonstrated an essential role of a proximal consensus CArG element in response to MYOCD/SRF in vitro. To validate the in vivo role of this CArG element, we generated CArG mutant mice via CRISPR-Cas9 genome editing. While the CArG mutation had no impact on the expression of surrounding genes, it abolished Mymsl expression in SMCs, but not skeletal and cardiac muscle. Chromatin immunoprecipitation assays (ChIPs) showed decreased SRF binding to CArG region in mutants whereas the enrichment of H3K79Me2 remained the same. RNA-seq analysis showed a downregulation of matrix genes in aortas from Mymsl knockout mice, which was further validated in injured carotid arteries. Our study defined the transcriptional control of a novel lncRNA in SMCs via a single transcription factor binding site, which may offer a new strategy for generating SMC-specific knockout mouse models. We also provided in vivo evidence supporting the potential importance of Mymsl in vascular pathophysiology.

Keywords: CRISPR genome editing; Long noncoding RNA; Transcription factor; Vascular smooth muscle.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aorta / metabolism
  • Blood Vessels / metabolism*
  • Cell Differentiation
  • Down-Regulation
  • Extracellular Matrix / metabolism
  • Gene Editing
  • Genome
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mutation / genetics
  • Myocytes, Cardiac / metabolism
  • Myocytes, Smooth Muscle / metabolism*
  • Nuclear Proteins / metabolism
  • Open Reading Frames / genetics
  • Phenotype
  • RNA, Long Noncoding / genetics
  • RNA, Long Noncoding / metabolism*
  • Regulatory Sequences, Nucleic Acid / genetics*
  • Serum Response Factor / metabolism
  • Trans-Activators / metabolism
  • Transcription, Genetic*

Substances

  • Nuclear Proteins
  • RNA, Long Noncoding
  • Serum Response Factor
  • Trans-Activators
  • myocardin