mRNA expression, splicing and editing in the embryonic and adult mouse cerebral cortex

被引:132
作者
Dillman, Allissa A. [1 ,2 ]
Hauser, David N. [1 ,3 ]
Gibbs, J. Raphael [4 ,5 ,6 ]
Nalls, Michael A. [7 ]
McCoy, Melissa K. [1 ]
Rudenko, Iakov N. [1 ]
Galter, Dagmar [2 ]
Cookson, Mark R. [1 ]
机构
[1] NIA, Cell Biol & Gene Express Sect, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
[2] Karolinska Inst, Dept Neurosci, Stockholm, Sweden
[3] Brown Univ, Natl Inst Hlth Grad Partnership Program, Dept Neurosci, Providence, RI 02912 USA
[4] NIA, Computat Biol Unit, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
[5] UCL, Inst Neurol, Reta Lila Weston Labs, London, England
[6] UCL, Inst Neurol, Dept Mol Neurosci, London, England
[7] NIA, Mol Genet Sect, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院; 瑞典研究理事会;
关键词
GLOBAL REGULATION; GENOME; POINT;
D O I
10.1038/nn.3332
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The complexity of the adult brain is a result of both developmental processes and experience-dependent circuit formation. One way to look at the differences between embryonic and adult brain is to examine gene expression. Previous studies have used microarrays to address this in a global manner. However, the transcriptome is more complex than gene expression levels alone, as alternative splicing and RNA editing generate a diverse set of mature transcripts. Here we report a high-resolution transcriptome data set of mouse cerebral cortex at embryonic and adult stages using RNA sequencing (RNA-Seq). We found many differences in gene expression, splicing and RNA editing between embryonic and adult cerebral cortex. Each data set was validated technically and biologically, and in each case we found our RNA-Seq observations to have predictive validity. We provide this data set and analysis as a resource for understanding gene expression in the embryonic and adult cerebral cortex.
引用
收藏
页码:499 / U178
页数:9
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