PI3K/Akt-dependent functions of TFII-I transcription factors in mouse embryonic stem cells

被引:12
|
作者
Chimge, Nyam-Osor [1 ]
Makeyev, Aleksandr V. [1 ]
Waigel, Sabine J. [2 ]
Enkhmandakh, Badam [1 ]
Bayarsaihan, Dashzeveg [1 ]
机构
[1] Univ Connecticut, Ctr Hlth, Dept Reconstruct Sci, Ctr Regenerat Med & Skeletal Dev,Sch Dent, Farmington, CT 06030 USA
[2] Univ Louisville, Brown Canc Ctr, Louisville, KY 40202 USA
关键词
EMBRYONIC STEM CELLS; Gtf2i; Gtf2ird1; EPIGENETICS; TFII-I; PHOSPHOINOSITOL; 3-KINASE; SELF-RENEWAL; PLURIPOTENCY; EXPRESSION; GENES; PREIMPLANTATION; IDENTIFICATION; METHYLATION; ACTIVATION; INHIBITOR; FAMILY;
D O I
10.1002/jcb.23441
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
Activation of PI3K/Akt signaling is sufficient to maintain the pluripotency of mouse embryonic stem cells (mESC) and results in down-regulation of Gtf2i and Gtf2ird1 encoding TFII-I family transcription factors. To investigate how these genes might be involved in the process of embryonic stem cell differentiation, we performed expression microarray profiling of mESC upon inhibition of PI3K by LY294002. This analysis revealed significant alterations in expression of genes for specific subsets of chromatin-modifying enzymes. Surprisingly, genome-wide promoter ChIP-chip mapping indicated that the majority of differently expressed genes could be direct targets of TFII-I regulation. The data support the hypothesis that upregulation of TFII-I factors leads to activation of a specific group of developmental genes during mESC differentiation. J. Cell. Biochem. 113: 11221131, 2012. (c) 2011 Wiley Periodicals, Inc.
引用
收藏
页码:1122 / 1131
页数:10
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