Dissecting Oct3/4-Regulated Gene Networks in Embryonic Stem Cells by Expression Profiling

被引:140
作者
Matoba, Ryo [1 ]
Niwa, Hitoshi [2 ]
Masui, Shinji [2 ]
Ohtsuka, Satoshi [2 ]
Carter, Mark G. [1 ]
Sharov, Alexei A. [1 ]
Ko, Minoru S. H. [1 ]
机构
[1] NIA, Dev Genom & Aging Sect, Genet Lab, NIH, Baltimore, MD 21224 USA
[2] RIKEN, Ctr Dev Biol, Lab Pluripotent Cell Studies, Kobe, Hyogo, Japan
来源
PLOS ONE | 2006年 / 1卷 / 01期
关键词
D O I
10.1371/journal.pone.0000026
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
POU transcription factor Pou5f1 (Oct3/4) is required to maintain ES cells in an undifferentiated state. Here we show that global expression profiling of Oct3/4-manipulated ES cells delineates the downstream target genes of Oct3/4. Combined with data from genome-wide chromatin-immunoprecipitation (ChIP) assays, this analysis identifies not only primary downstream targets of Oct3/4, but also secondary or tertiary targets. Furthermore, the analysis also reveals that downstream target genes are regulated either positively or negatively by Oct3/4. Identification of a group of genes that show both activation and repression depending on Oct3/4 expression levels provides a possible mechanism for the requirement of appropriate Oct3/4 expression to maintain undifferentiated ES cells. As a proof-of-principle study, one of the downstream genes, Tcl1, has been analyzed in detail. We show that Oct3/4 binds to the promoter region of Tcl1 and activates its transcription. We also show that Tcl1 is involved in the regulation of proliferation, but not differentiation, in ES cells. These findings suggest that the global expression profiling of gene-manipulated ES cells can help to delineate the structure and dynamics of gene regulatory networks.
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页数:15
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