Frontiers in Molecular Neuroscience (Oct 2019)

MiR-137 Deficiency Causes Anxiety-Like Behaviors in Mice

  • Hai-Liang Yan,
  • Xiao-Wen Sun,
  • Xiao-Wen Sun,
  • Zhi-Meng Wang,
  • Zhi-Meng Wang,
  • Pei-Pei Liu,
  • Pei-Pei Liu,
  • Ting-Wei Mi,
  • Cong Liu,
  • Cong Liu,
  • Ying-Ying Wang,
  • Ying-Ying Wang,
  • Xuan-Cheng He,
  • Xuan-Cheng He,
  • Hong-Zhen Du,
  • Hong-Zhen Du,
  • Chang-Mei Liu,
  • Chang-Mei Liu,
  • Chang-Mei Liu,
  • Zhao-Qian Teng,
  • Zhao-Qian Teng,
  • Zhao-Qian Teng

DOI
https://doi.org/10.3389/fnmol.2019.00260
Journal volume & issue
Vol. 12

Abstract

Read online

Anxiety and depression are major public health concerns worldwide. Although genome-wide association studies have identified several genes robustly associated with susceptibility for these disorders, the molecular and cellular mechanisms associated with anxiety and depression is largely unknown. Reduction of microRNA-137 (miR-137) level has been implicated in the etiology of major depressive disorder. However, little is known about the in vivo impact of the loss of miR-137 on the biology of anxiety and depression. Here, we generated a forebrain-specific miR-137 knockout mouse line, and showed that miR-137 is critical for dendritic and synaptic growth in the forebrain. Mice with miR-137 loss-of-function exhibit anxiety-like behavior, and impaired spatial learning and memory. We then observe an elevated expression of EZH2 in the forebrain of miR-137 knockout mice, and provide direct evidence that knockdown of EZH2 can rescue anxious phenotypes associated with the loss of miR-137. Together our results suggest that loss of miR-137 contributes to the etiology of anxiety, and EZH2 might be a potential therapeutic target for anxiety and depressive phenotypes associated with the dysfunction of miR-137.

Keywords