Affiliations 

  • 1 Institute of Reproductive and Developmental Biology, Department of Surgery and Cancer, Imperial College London, Du Cane Road, London W12 ONN, UK National University of Malaysia, Kuala Lumpur, Malaysia
  • 2 Institute of Reproductive and Developmental Biology, Department of Surgery and Cancer, Imperial College London, Du Cane Road, London W12 ONN, UK
  • 3 Department of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, UK
  • 4 Wellcome Trust Genome Campus, Hinxton, CB10 S1A, UK
  • 5 University of Queensland Centre for Clinical Research, Brisbane, Australia
  • 6 Imperial Centre for Translational and Experimental Medicine (ICTEM), Department of Surgery and Cancer, Imperial College London, Du Cane Road, London W12 ONN, UK
  • 7 Max-Planck-Institut für Biochemi, Am Klopferspitz 1, D-82152 Martinsried, Germany University of Regensburg, Universitaetsstrasse, Germany
  • 8 Institute of Reproductive and Developmental Biology, Department of Surgery and Cancer, Imperial College London, Du Cane Road, London W12 ONN, UK n.dibb@imperial.ac.uk
Nucleic Acids Res, 2014 Aug;42(14):9424-35.
PMID: 25056318 DOI: 10.1093/nar/gku656

Abstract

We have sequenced miRNA libraries from human embryonic, neural and foetal mesenchymal stem cells. We report that the majority of miRNA genes encode mature isomers that vary in size by one or more bases at the 3' and/or 5' end of the miRNA. Northern blotting for individual miRNAs showed that the proportions of isomiRs expressed by a single miRNA gene often differ between cell and tissue types. IsomiRs were readily co-immunoprecipitated with Argonaute proteins in vivo and were active in luciferase assays, indicating that they are functional. Bioinformatics analysis predicts substantial differences in targeting between miRNAs with minor 5' differences and in support of this we report that a 5' isomiR-9-1 gained the ability to inhibit the expression of DNMT3B and NCAM2 but lost the ability to inhibit CDH1 in vitro. This result was confirmed by the use of isomiR-specific sponges. Our analysis of the miRGator database indicates that a small percentage of human miRNA genes express isomiRs as the dominant transcript in certain cell types and analysis of miRBase shows that 5' isomiRs have replaced canonical miRNAs many times during evolution. This strongly indicates that isomiRs are of functional importance and have contributed to the evolution of miRNA genes.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.