Global Transcriptome Profiling of Genes that Are Differentially Regulated During Differentiation of Mouse Embryonic Neural Stem Cells into Astrocytes

被引:16
|
作者
Han, Dalmuri [1 ]
Choi, Mi Ran [1 ]
Jung, Kyoung Hwa [1 ]
Kim, Namshin [3 ]
Kim, Se Kye [1 ]
Chai, Jin Choul [1 ]
Lee, Young Seek [1 ]
Chai, Young Gyu [1 ,2 ]
机构
[1] Hanyang Univ, Dept Mol & Life Sci, Ansan 426791, South Korea
[2] Hanyang Univ, Dept Nanobiotechnol, Seoul 131791, South Korea
[3] Korea Res Inst Biosci & Biotechnol, Korean Bioinformat Ctr, Taejon 305806, South Korea
基金
新加坡国家研究基金会;
关键词
Neural stem cells; Astrocytes; Cell differentiation; TGF beta; WNTs; IN-VIVO; RNA-SEQ; EXPRESSION; SPECIFICATION; IDENTIFICATION; OLIGODENDROCYTES; PLURIPOTENT; INSIGHTS; CULTURES; DATABASE;
D O I
10.1007/s12031-014-0382-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many genes are associated with the differentiation of neural stem cells (NSCs) into astrocytes, the most abundant and functionally diverse population of glial cells in the central nervous system, particularly in the brain. In the present study, we differentiated NSCs from the forebrain of embryonic day 14.5 mouse embryos into astrocytes over 1 and 7 days. We identified transcriptomes of NSCs and astrocytes using RNA sequencing and analyzed enriched gene networks, signal pathways, and ontology. To identify important regulators of differentiation, we performed gene clustering according to expression patterns and promoter CG types. Our data show that genes related to system development, including Fbln2, Bcan, Ncam1, Itih3, Tnr, and Vcan, regulate NSC differentiation through WNT/beta-catenin and epithelial to mesenchymal transition pathways. We identified many CG-rich promoter genes related to basic cellular maintenance such as transcription, translation, and structural components and CG-poor promoter genes that are highly associated with cell-type-specific functions or play important roles during development. Our study provides a foundation for further research on NSC differentiation and the future application of stem cells.
引用
收藏
页码:109 / 125
页数:17
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