Social interaction-induced activation of RNA splicing in the amygdala of microbiome-deficient mice.
Roman M StillingGerard M MoloneyFeargal Joseph RyanAlan E HobanThomaz F S BastiaanssenFergus ShanahanGerard ClarkeMarcus Joakim ClaessonTimothy G DinanJohn F CryanPublished in: eLife (2018)
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).
Keyphrases
- healthcare
- mental health
- gene expression
- high fat diet induced
- functional connectivity
- resting state
- autism spectrum disorder
- dna methylation
- type diabetes
- adipose tissue
- insulin resistance
- skeletal muscle
- white matter
- endothelial cells
- electronic health record
- machine learning
- wild type
- attention deficit hyperactivity disorder
- stress induced
- artificial intelligence
- mechanical ventilation
- acute respiratory distress syndrome
- drug induced
- genetic diversity
- data analysis