4.8 Article

DeCoN: Genome-wide Analysis of In Vivo Transcriptional Dynamics during Pyramidal Neuron Fate Selection in Neocortex

期刊

NEURON
卷 85, 期 2, 页码 275-288

出版社

CELL PRESS
DOI: 10.1016/j.neuron.2014.12.024

关键词

-

资金

  1. NSF Postdoctoral Fellowship in Biology
  2. Sternlicht Director's Fund Fellowship
  3. NIH [DP2OD006670, P01 GM099117, R01 MH102416, NS062489, NS073124, NS078164]
  4. Center for Cell Circuits [P50 HG006193-01]
  5. New York Stem Cell Foundation
  6. Harvard Stem Cell Institute

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据