Longitudinal assessment of neuronal 3D genomes in mouse prefrontal cortex.
Amanda C MitchellBehnam JavidfarLucy K BicksRachael NeveKrassimira GarbettSharon S LanderKaroly MirnicsHirofumi MorishitaMarcelo A WoodYan JiangInna Gaisler-SalomonSchahram AkbarianPublished in: Nature communications (2016)
Neuronal epigenomes, including chromosomal loopings moving distal cis-regulatory elements into proximity of target genes, could serve as molecular proxy linking present-day-behaviour to past exposures. However, longitudinal assessment of chromatin state is challenging, because conventional chromosome conformation capture assays essentially provide single snapshots at a given time point, thus reflecting genome organization at the time of brain harvest and therefore are non-informative about the past. Here we introduce 'NeuroDam' to assess epigenome status retrospectively. Short-term expression of the bacterial DNA adenine methyltransferase Dam, tethered to the Gad1 gene promoter in mouse prefrontal cortex neurons, results in stable G(methyl)ATC tags at Gad1-bound chromosomal contacts. We show by NeuroDam that mice with defective cognition 4 months after pharmacological NMDA receptor blockade already were affected by disrupted chromosomal conformations shortly after drug exposure. Retrospective profiling of neuronal epigenomes is likely to illuminate epigenetic determinants of normal and diseased brain development in longitudinal context.
Keyphrases
- prefrontal cortex
- copy number
- genome wide
- dna methylation
- cerebral ischemia
- cross sectional
- resting state
- gene expression
- white matter
- transcription factor
- functional connectivity
- poor prognosis
- subarachnoid hemorrhage
- single molecule
- genome wide identification
- blood brain barrier
- emergency department
- high throughput
- circulating tumor
- spinal cord
- single cell
- molecular dynamics simulations
- minimally invasive
- multiple sclerosis
- type diabetes
- crystal structure