Klf4 cooperates with Oct3/4 and Sox2 to activate the Lefty1 core promoter in embryonic stem cells

被引:195
作者
Nakatake, Yuhki
Fukui, Nobutaka
Iwamatsu, Yuko
Masui, Shinji
Takahashi, Kadue
Yagi, Rika
Yagi, Kiyohito
Miyazaki, Jun-ichi
Matoba, Ryo
Ko, Minoru S. H.
Niwa, Hitoshi
机构
[1] RIKEN, Ctr Dev Biol, Lab Pluripotent Cell Studies, Chuo Ku, Kobe, Hyogo 6500047, Japan
[2] Osaka Univ, Grad Sch Pharmaceut Sci, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Grad Sch Med, Course Adv Med, Area Mol Therapeut, Suita, Osaka 5650871, Japan
[4] NIA, Dev Genom & Aging Sect, Genet Lab, NIH, Baltimore, MD 21224 USA
[5] Kobe Univ, Grad Sch Med, Lab Dev & Regenerat Med, Chuo Ku, Kobe, Hyogo 6500017, Japan
关键词
D O I
10.1128/MCB.00468-06
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
Although the POU transcription factor Oct3/4 is pivotal in maintaining self renewal of embryonic stem (ES) cells, little is known of its molecular mechanisms. We previously reported that the N-terminal transactivation domain of Oct3/4 is required for activation of Lefty1 expression (H. Niwa, S. Masui, I. Chambers, A. G. Smith, and J. Miyazaki, Mol. Cell. Biol. 22:1526-1536, 2002). Here we test whether Lefty1 is a direct target of Oct3/4. We identified an ES cell-specific enhancer upstream of the Lefty1 promoter that contains binding sites for Oct3/4 and Sox2. Unlike other known Oct3/4-Sox2-dependent enhancers, however, this enhancer element could not be activated by Oct3/4 and Sox2 in differentiated cells. By functional screening of ES-specific transcription factors, we found that Kruppel-like factor 4 (KIN) cooperates with Oct3/4 and Sox2 to activate Lefty1 expression, and that KIN acts as a mediating factor that specifically binds to the proximal element of the Lefty1 promoter. DNA microarray analysis revealed that a subset of putative Oct3/4 target genes may be regulated in the same manner. Our findings shed light on a novel function of Oct3/4 in ES cells.
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收藏
页码:7772 / 7782
页数:11
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