DeCoN: genome-wide analysis of in vivo transcriptional dynamics during pyramidal neuron fate selection in neocortex.

Neuron
Authors
Keywords
Abstract

UNLABELLED: Neuronal development requires a complex choreography of transcriptional decisions to obtain specific cellular identities. Realizing the ultimate goal of identifying genome-wide signatures that define and drive specific neuronal fates has been hampered by enormous complexity in both time and space during development. Here, we have paired high-throughput purification of pyramidal neuron subclasses with deep profiling of spatiotemporal transcriptional dynamics during corticogenesis to resolve lineage choice decisions. We identified numerous features ranging from spatial and temporal usage of alternative mRNA isoforms and promoters to a host of mRNA genes modulated during fate specification. Notably, we uncovered numerous long noncoding RNAs with restricted temporal and cell-type-specific expression. To facilitate future exploration, we provide an interactive online database to enable multidimensional data mining and dissemination. This multifaceted study generates a powerful resource and informs understanding of the transcriptional regulation underlying pyramidal neuron diversity in the neocortex.

VIDEO ABSTRACT:

Year of Publication
2015
Journal
Neuron
Volume
85
Issue
2
Pages
275-288
Date Published
2015 Jan 21
ISSN
1097-4199
URL
DOI
10.1016/j.neuron.2014.12.024
PubMed ID
25556833
PubMed Central ID
PMC4430475
Links
Grant list
DP2 OD006670 / OD / NIH HHS / United States
R01 NS078164 / NS / NINDS NIH HHS / United States
P01 GM099117 / GM / NIGMS NIH HHS / United States
R01 MH101268 / MH / NIMH NIH HHS / United States
F30 NS062489 / NS / NINDS NIH HHS / United States
R01 MH102416 / MH / NIMH NIH HHS / United States
NS073124 / NS / NINDS NIH HHS / United States
R01 NS073124 / NS / NINDS NIH HHS / United States
P50 HG006193 / HG / NHGRI NIH HHS / United States
P50 HG006193-01 / HG / NHGRI NIH HHS / United States
NIH R01 MH102416 / MH / NIMH NIH HHS / United States
DP2OD006670 / OD / NIH HHS / United States
NS078164 / NS / NINDS NIH HHS / United States
NS062489 / NS / NINDS NIH HHS / United States