The muscle-specific microRNA miR-1 regulates cardiac arrhythmogenic potential by targeting GJA1 and KCNJ2

Nat Med. 2007 Apr;13(4):486-91. doi: 10.1038/nm1569. Epub 2007 Apr 1.

Abstract

MicroRNAs (miRNAs) are endogenous noncoding RNAs, about 22 nucleotides in length, that mediate post-transcriptional gene silencing by annealing to inexactly complementary sequences in the 3'-untranslated regions of target mRNAs. Our current understanding of the functions of miRNAs relies mainly on their tissue-specific or developmental stage-dependent expression and their evolutionary conservation, and therefore is primarily limited to their involvement in developmental regulation and oncogenesis. Of more than 300 miRNAs that have been identified, miR-1 and miR-133 are considered to be muscle specific. Here we show that miR-1 is overexpressed in individuals with coronary artery disease, and that when overexpressed in normal or infarcted rat hearts, it exacerbates arrhythmogenesis. Elimination of miR-1 by an antisense inhibitor in infarcted rat hearts relieved arrhythmogenesis. miR-1 overexpression slowed conduction and depolarized the cytoplasmic membrane by post-transcriptionally repressing KCNJ2 (which encodes the K(+) channel subunit Kir2.1) and GJA1 (which encodes connexin 43), and this likely accounts at least in part for its arrhythmogenic potential. Thus, miR-1 may have important pathophysiological functions in the heart, and is a potential antiarrhythmic target.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / physiology*
  • Animals
  • Arrhythmias, Cardiac / genetics
  • Arrhythmias, Cardiac / metabolism*
  • Base Sequence
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2 / metabolism
  • Connexin 43 / genetics
  • Connexin 43 / metabolism*
  • Coronary Artery Disease / genetics
  • Coronary Artery Disease / metabolism*
  • DNA Primers
  • Electrocardiography
  • Gene Expression Regulation*
  • Humans
  • MicroRNAs / metabolism*
  • Molecular Sequence Data
  • Mutagenesis
  • Myogenic Regulatory Factors / metabolism
  • Potassium Channels, Inwardly Rectifying / genetics
  • Potassium Channels, Inwardly Rectifying / metabolism*
  • Rats
  • Sequence Analysis, DNA
  • Signal Transduction / physiology

Substances

  • Connexin 43
  • DNA Primers
  • GJA1 protein, human
  • KCNJ2 protein, human
  • MicroRNAs
  • Myogenic Regulatory Factors
  • Potassium Channels, Inwardly Rectifying
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2

Associated data

  • GENBANK/AC103987
  • GENBANK/AF153818
  • GENBANK/BC081842
  • GENBANK/DQ066650
  • RefSeq/NM_000165
  • RefSeq/NW_047343