Social interaction-induced activation of RNA splicing in the amygdala of microbiome-deficient mice

Elife. 2018 May 29:7:e33070. doi: 10.7554/eLife.33070.

Abstract

Social behaviour is regulated by activity of host-associated microbiota across multiple species. However, the molecular mechanisms mediating this relationship remain elusive. We therefore determined the dynamic, stimulus-dependent transcriptional regulation of germ-free (GF) and GF mice colonised post weaning (exGF) in the amygdala, a brain region critically involved in regulating social interaction. In GF mice the dynamic response seen in controls was attenuated and replaced by a marked increase in expression of splicing factors and alternative exon usage in GF mice upon stimulation, which was even more pronounced in exGF mice. In conclusion, we demonstrate a molecular basis for how the host microbiome is crucial for a normal behavioural response during social interaction. Our data further suggest that social behaviour is correlated with the gene-expression response in the amygdala, established during neurodevelopment as a result of host-microbe interactions. Our findings may help toward understanding neurodevelopmental events leading to social behaviour dysregulation, such as those found in autism spectrum disorders (ASDs).

Keywords: Social behaviour; activity-dependent transcription; amygdala; autism; microbiome; mouse; neurodevelopment; neuroscience.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amygdala / metabolism*
  • Amygdala / physiopathology
  • Animal Communication*
  • Animals
  • Autism Spectrum Disorder / genetics
  • Autism Spectrum Disorder / microbiology
  • Autism Spectrum Disorder / physiopathology
  • Disease Models, Animal
  • Gastrointestinal Microbiome / physiology*
  • Germ-Free Life
  • Male
  • Mice
  • Nerve Tissue Proteins / genetics*
  • Nerve Tissue Proteins / metabolism
  • Neurogenesis / genetics
  • RNA Splicing Factors / genetics*
  • RNA Splicing Factors / metabolism
  • RNA Splicing*
  • Weaning

Substances

  • Nerve Tissue Proteins
  • RNA Splicing Factors