Transcriptome coexpression map of human embryonic stem cells

被引:23
作者
Li, Huai
Liu, Ying
Shin, Soojung
Sun, Yu
Loring, Jeanne F.
Mattson, Mark P.
Rao, Mahendra S. [1 ]
Zhan, Ming
机构
[1] NIA, Bioinformat Unit, Branch Res Resources, NIH, Baltimore, MD 21224 USA
[2] NIA, Neurosci Lab, NIH, Baltimore, MD 21224 USA
[3] Johns Hopkins Univ, Sch Med, Neurosci Program, Baltimore, MD 21224 USA
[4] Burnham Inst, La Jolla, CA 92037 USA
[5] CRL, Invitrogen Corp, Carlsbad, CA 92008 USA
关键词
D O I
10.1186/1471-2164-7-103
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
Background: Human embryonic stem (ES) cells hold great promise for medicine and science. The transcriptome of human ES cells has been studied in detail in recent years. However, no systematic analysis has yet addressed whether gene expression in human ES cells may be regulated in chromosomal domains, and no chromosomal domains of coexpression have been identified. Results: We report the first transcriptome coexpression map of the human ES cell and the earliest stage of ES differentiation, the embryoid body (EB), for the analysis of how transcriptional regulation interacts with genomic structure during ES self-renewal and differentiation. We determined the gene expression profiles from multiple ES and EB samples and identified chromosomal domains showing coexpression of adjacent genes on the genome. The coexpression domains were not random, with significant enrichment in chromosomes 8, 11, 16, 17, 19, and Y in the ES state, and 6, 11, 17, 19 and 20 in the EB state. The domains were significantly associated with Giemsa-negative bands in EB, yet showed little correlation with known cytogenetic structures in ES cells. Different patterns of coexpression were revealed by comparative transcriptome mapping between ES and EB. Conclusion: The findings and methods reported in this investigation advance our understanding of how genome organization affects gene expression in human ES cells and help to identify new mechanisms and pathways controlling ES self-renewal or differentiation.
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页数:15
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