A genomic lifespan program that reorganises the young adult brain is targeted in schizophrenia.
Nathan G SkeneMarcia RoySeth G N GrantPublished in: eLife (2017)
The genetic mechanisms regulating the brain and behaviour across the lifespan are poorly understood. We found that lifespan transcriptome trajectories describe a calendar of gene regulatory events in the brain of humans and mice. Transcriptome trajectories defined a sequence of gene expression changes in neuronal, glial and endothelial cell-types, which enabled prediction of age from tissue samples. A major lifespan landmark was the peak change in trajectories occurring in humans at 26 years and in mice at 5 months of age. This species-conserved peak was delayed in females and marked a reorganization of expression of synaptic and schizophrenia-susceptibility genes. The lifespan calendar predicted the characteristic age of onset in young adults and sex differences in schizophrenia. We propose a genomic program generates a lifespan calendar of gene regulation that times age-dependent molecular organization of the brain and mutations that interrupt the program in young adults cause schizophrenia.
Keyphrases
- young adults
- bipolar disorder
- gene expression
- resting state
- white matter
- genome wide
- quality improvement
- cerebral ischemia
- depressive symptoms
- functional connectivity
- endothelial cells
- copy number
- dna methylation
- type diabetes
- single cell
- childhood cancer
- transcription factor
- high fat diet induced
- rna seq
- neuropathic pain
- multiple sclerosis
- single molecule
- blood brain barrier
- spinal cord
- cancer therapy
- binding protein
- insulin resistance
- genetic diversity