Literature DB >> 28893375

A genomic lifespan program that reorganises the young adult brain is targeted in schizophrenia.

Nathan G Skene1, Marcia Roy1, Seth Gn Grant1.   

Abstract

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.

Entities:  

Keywords:  Schizophrenia; evolutionary biology; genomics; human; mouse; neuroscience; post-mortem; transcriptomics

Mesh:

Substances:

Year:  2017        PMID: 28893375      PMCID: PMC5595438          DOI: 10.7554/eLife.17915

Source DB:  PubMed          Journal:  Elife        ISSN: 2050-084X            Impact factor:   8.140


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