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Longitudinal assessment of neuronal 3D genomes in mouse prefrontal cortex
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 chromoso...
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Published in: | Nature communications 2016-09, Vol.7 (1), p.12743-12743, Article 12743 |
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Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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.
Chromosome conformation is a dynamic process, especially in brain. Here, Mitchell and colleagues devise a method they call NeuroDam that can prospectively tag chromosome conformation in the mouse brain
in vivo
, and longitudinally assess long range chromosome looping weeks and months later. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/ncomms12743 |