The nuclear matrix protein Matr3 regulates processing of the synaptic microRNA-138-5p

Neurobiol Learn Mem. 2019 Mar:159:36-45. doi: 10.1016/j.nlm.2019.02.008. Epub 2019 Feb 18.

Abstract

microRNA-dependent post-transcriptional control represents an important gene-regulatory layer in post-mitotic neuronal development and synaptic plasticity. We recently identified the brain-enriched miR-138 as a negative regulator of dendritic spine morphogenesis in rat hippocampal neurons. A potential involvement of miR-138 in cognition is further supported by a recent GWAS study on memory performance in a cohort of aged (>60 years) individuals. The expression of miR-138, which is encoded in two independent genomic loci (miR-138-1 and -2), is subject to both cell-type and developmental stage-specific regulation, the underlying molecular mechanisms however are poorly understood. Here, we show that miR-138-2 is the primary source of mature miR-138 in developing rat hippocampal neurons. Furthermore, we obtained evidence for the regulation of miR-138-2 biogenesis at the level of primary miRNA processing. Using biochemical pull-down assays, we identified the nuclear matrix protein Matrin-3 as pri/pre-miR-138 interacting protein and mapped the interaction to the pri/pre-miR-138-2 loop region. Matrin-3 loss-of-function experiments in HEK293 cells and primary neurons together with protein localization studies suggest an inhibitory function of Matrin-3 in nuclear pri-miR-138-2 processing. Together, our experiments unravel a new mechanism of miR-138 regulation in neurons, with important implications for miR-138 regulation during neuronal development, synaptic plasticity and memory-related processes.

Keywords: Matrin-3; RNA-binding protein; Synaptic plasticity; miR-138; microRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Embryo, Mammalian
  • HEK293 Cells
  • Hippocampus / metabolism*
  • Humans
  • MicroRNAs / metabolism*
  • Neuronal Plasticity / physiology*
  • Nuclear Matrix-Associated Proteins / physiology*
  • RNA-Binding Proteins / physiology*
  • Rats
  • Rats, Sprague-Dawley
  • Rats, Transgenic

Substances

  • MATR3 protein, human
  • MIRN138 microRNA, human
  • MIRN138 microRNA, rat
  • MicroRNAs
  • Nuclear Matrix-Associated Proteins
  • RNA-Binding Proteins