MicroRNA-138 and SIRT1 form a mutual negative feedback loop to regulate mammalian axon regeneration

  1. Feng-Quan Zhou1,3,5
  1. 1Department of Orthopaedic Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287, USA;
  2. 2Department of Orthopaedic Surgery, Affiliated Hospital of Guilin Medical University, Guilin, Guangxi 541001, China;
  3. 3Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287, USA
    1. 4 These authors contributed equally to this work.

    Abstract

    Regulated gene expression determines the intrinsic ability of neurons to extend axons, and loss of such ability is the major reason for the failed axon regeneration in the mature mammalian CNS. MicroRNAs and histone modifications are key epigenetic regulators of gene expression, but their roles in mammalian axon regeneration are not well explored. Here we report microRNA-138 (miR-138) as a novel suppressor of axon regeneration and show that SIRT1, the NAD-dependent histone deacetylase, is the functional target of miR-138. Importantly, we provide the first evidence that miR-138 and SIRT1 regulate mammalian axon regeneration in vivo. Moreover, we found that SIRT1 also acts as a transcriptional repressor to suppress the expression of miR-138 in adult sensory neurons in response to peripheral nerve injury. Therefore, miR-138 and SIRT1 form a mutual negative feedback regulatory loop, which provides a novel mechanism for controlling intrinsic axon regeneration ability.

    Keywords

    Footnotes

    • Received November 5, 2012.
    • Accepted June 3, 2013.
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