Environmental enrichment increases transcriptional and epigenetic differentiation between mouse dorsal and ventral dentate gyrus.
Tie-Yuan ZhangChristopher L KeownXianglan WenJunhao LiDulcie A VousdenChristoph AnackerUrvashi BhattacharyyaRichard RyanJosie DiorioNicholas O'TooleJason P LerchEran A MukamelMichael J MeaneyPublished in: Nature communications (2018)
Early life experience influences stress reactivity and mental health through effects on cognitive-emotional functions that are, in part, linked to gene expression in the dorsal and ventral hippocampus. The hippocampal dentate gyrus (DG) is a major site for experience-dependent plasticity associated with sustained transcriptional alterations, potentially mediated by epigenetic modifications. Here, we report comprehensive DNA methylome, hydroxymethylome and transcriptome data sets from mouse dorsal and ventral DG. We find genome-wide transcriptional and methylation differences between dorsal and ventral DG, including at key developmental transcriptional factors. Peripubertal environmental enrichment increases hippocampal volume and enhances dorsal DG-specific differences in gene expression. Enrichment also enhances dorsal-ventral differences in DNA methylation, including at binding sites of the transcription factor NeuroD1, a regulator of adult neurogenesis. These results indicate a dorsal-ventral asymmetry in transcription and methylation that parallels well-known functional and anatomical differences, and that may be enhanced by environmental enrichment.
Keyphrases
- spinal cord
- gene expression
- dna methylation
- genome wide
- neuropathic pain
- transcription factor
- spinal cord injury
- mental health
- early life
- prefrontal cortex
- cerebral ischemia
- human health
- risk assessment
- copy number
- single cell
- machine learning
- big data
- life cycle
- deep learning
- young adults
- heat shock
- genome wide identification
- neural stem cells