The role of Zfp352 in the regulation of transient expression of 2-cell specific genes in mouse embryonic stem cells

被引:2
作者
Mwalilino, Lusubilo [1 ]
Yamane, Mariko [1 ,2 ,3 ]
Ishiguro, Kei-ichiro [4 ]
Usuki, Shingo [5 ]
Endoh, Mitsuhiro [1 ]
Niwa, Hitoshi [1 ]
机构
[1] Kumamoto Univ, Inst Mol Embryol & Genet, Dept Pluripotent Stem Cell Biol, 2-2-1 Honjo,Chuo Ku, Kumamoto 8600811, Japan
[2] Tokyo Med & Dent Univ, Med Res Inst, Dept Funct Genome Informat, Div Med Genom, Tokyo, Japan
[3] RIKEN Ctr Biosyst Dynam Res, Lab Bioinformat Res, Kobe, Japan
[4] Kumamoto Univ, Inst Mol Embryol & Genet, Dept Chromosome Biol, Kumamoto, Japan
[5] Kumamoto Univ, Liaison Lab Res Promot Ctr, IMEG, Kumamoto, Japan
关键词
embryonic stem cells; transcriptional regulation; ZSCAN4; RETROTRANSPOSONS; TRANSCRIPTION; MERVL; DUX;
D O I
10.1111/gtc.13070
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mouse ES cell populations contain a minor sub-population that expresses genes specifically expressed in 2-cell stage embryos. This sub-population consists of 2-cell-gene labeled cells (2CLCs) generated by the transient activation of the 2-cell specific genes initiated by the master regulator, Dux. However, the mechanism regulating the transient expression remains largely unclear. Here we reported a novel function of Zfp352, one of the 2-cell specific genes, in regulating the 2CLC sub-population. Zfp352 encodes zinc-finger transcription factor belonging to the Klf family. Dux transiently activates Zfp352 after the activation of Zscan4c in a subset of the 2CLC subpopulation. Interestingly, in the reporter assay, the transcriptional activation of Zscan4c by Dux is strongly repressed by the co-expression of Zfp352. However, the knockout of Zfp352 resulted in the repression of a subset of the 2-cell-specific genes. These data suggest the dual roles of Zfp352 in regulating the transient activation of the 2-cell-specific genes.
引用
收藏
页码:831 / 844
页数:14
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