An RNA-Sequencing Transcriptome and Splicing Database of Glia, Neurons, and Vascular Cells of the Cerebral Cortex

被引:21
|
作者
Zhang, Ye [1 ]
Chen, Kenian [2 ,3 ]
Sloan, Steven A. [1 ]
Bennett, Mariko L. [1 ]
Scholze, Anja R. [1 ]
O'Keeffe, Sean [4 ]
Phatnani, Hemali P. [4 ]
Guarnieri, Paolo [7 ,9 ]
Caneda, Christine [1 ]
Ruderisch, Nadine [5 ]
Deng, Shuyun [2 ,3 ]
Liddelow, Shane A. [1 ,6 ]
Zhang, Chaolin [4 ,7 ,8 ]
Daneman, Richard [5 ]
Maniatis, Tom [4 ]
Barres, Ben A. [1 ]
Wu, Jia Qian [2 ,3 ]
机构
[1] Stanford Univ, Sch Med, Dept Neurobiol, Stanford, CA 94305 USA
[2] Univ Texas Houston, Med Sch Houston, Vivian L Smith Dept Neurosurg, Houston, TX 77057 USA
[3] Univ Texas, Inst Mol Med Brown, Ctr Stem Cell & Regenerat Med, Houston, TX 77057 USA
[4] Columbia Univ, Med Ctr, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[5] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
[6] Univ Melbourne, Dept Pharmacol & Therapeut, Parkville, Vic 3010, Australia
[7] Columbia Univ, Dept Syst Biol, New York, NY 10032 USA
[8] Columbia Univ, Ctr Motor Neuron Biol & Dis, New York, NY 10032 USA
[9] Columbia Univ, Herbert Irving Comprehens Canc Ctr, New York, NY 10032 USA
来源
JOURNAL OF NEUROSCIENCE | 2014年 / 34卷 / 36期
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
alternative splicing; astrocytes; microglia; oligodendrocytes; transcriptome; vascular cells; BRAIN ENERGY-METABOLISM; GENE-EXPRESSION; ADHESION MOLECULE; GENOMIC ANALYSIS; BINDING PROTEIN; NONCODING RNAS; STEM-CELLS; RAT-BRAIN; IN-VITRO; ASTROCYTES;
D O I
10.1523/JNEUROSCI.1860-14.2014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The major cell classes of the brain differ in their developmental processes, metabolism, signaling, and function. To better understand the functions and interactions of the cell types that comprise these classes, we acutely purified representative populations of neurons, astrocytes, oligodendrocyte precursor cells, newly formed oligodendrocytes, myelinating oligodendrocytes, microglia, endothelial cells, and pericytes from mouse cerebral cortex. We generated a transcriptome database for these eight cell types by RNA sequencing and used a sensitive algorithm to detect alternative splicing events in each cell type. Bioinformatic analyses identified thousands of new cell type-enriched genes and splicing isoforms that will provide novel markers for cell identification, tools for genetic manipulation, and insights into the biology of the brain. For example, our data provide clues as to how neurons and astrocytes differ in their ability to dynamically regulate glycolytic flux and lactate generation attributable to unique splicing of PKM2, the gene encoding the glycolytic enzyme pyruvate kinase. This dataset will provide a powerful new resource for understanding the development and function of the brain. To ensure the widespread distribution of these datasets, we have created a user-friendly website (http://web.stanford.edu/group/barres_lab/brain_rnaseq.html) that provides a platform for analyzing and comparing transciption and alternative splicing profiles for various cell classes in the brain.
引用
收藏
页码:11929 / 11947
页数:19
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