MicroRNA-mediated disruption of dendritogenesis during a critical period of development influences cognitive capacity later in life

Proc Natl Acad Sci U S A. 2017 Aug 22;114(34):9188-9193. doi: 10.1073/pnas.1706069114. Epub 2017 Aug 8.

Abstract

The prenatal period of cortical development is important for the establishment of neural circuitry and functional connectivity of the brain; however, the molecular mechanisms underlying this process remain unclear. Here we report that disruption of the actin-cytoskeletal network in the developing mouse prefrontal cortex alters dendritic morphogenesis and synapse formation, leading to enhanced formation of fear-related memory in adulthood. These effects are mediated by a brain-enriched microRNA, miR-9, through its negative regulation of diaphanous homologous protein 1 (Diap1), a key organizer of the actin cytoskeletal assembly. Our findings not only revealed important regulation of dendritogenesis and synaptogenesis during early brain development but also demonstrated a tight link between these early developmental events and cognitive functions later in life.

Keywords: Diap1; dendritogenesis; learning; memory; miR-9.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Cognition*
  • Formins
  • Gene Expression Regulation, Developmental
  • Male
  • Memory
  • Mice
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Neurogenesis*
  • Prefrontal Cortex / growth & development*
  • Prefrontal Cortex / metabolism*

Substances

  • Carrier Proteins
  • Diap1 protein, mouse
  • Formins
  • MIRN9 microRNA, mouse
  • MicroRNAs