Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation

被引:276
作者
Brandenberger, R
Wei, H
Zhang, S
Lei, S
Murage, J
Fisk, GJ
Li, Y
Xu, CH
Fang, R
Guegler, K
Rao, MS
Mandalam, R
Lebkowski, J
Stanton, LW
机构
[1] Geron Corp, Menlo Pk, CA 94025 USA
[2] Celera Genom, Rockville, MD 20850 USA
[3] NIA, Baltimore, MD 21224 USA
关键词
D O I
10.1038/nbt971
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
Human embryonic stem (hES) cells hold promise for generating an unlimited supply of cells for replacement therapies. To characterize hES cells at the molecular level, we obtained 148,453 expressed sequence tags (ESTs) from undifferentiated hES cells and three differentiated derivative subpopulations. Over 32,000 different transcripts expressed in hES cells were identified, of which more than 16,000 do not match closely any gene in the UniGene public database. Queries to this EST database revealed 532 significantly upregulated and 140 significantly downregulated genes in undifferentiated hES cells. These data highlight changes in the transcriptional network that occur when hES cells differentiate. Among the differentially regulated genes are several components of signaling pathways and transcriptional regulators that likely play key roles in hES cell growth and differentiation. The genomic data presented here may facilitate the derivation of clinically useful cell types from hES cells.
引用
收藏
页码:707 / 716
页数:10
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