Proviral Silencing in Embryonic Cells Is Regulated by Yin Yang 1

被引:55
作者
Schlesinger, Sharon [1 ,2 ]
Lee, Andreia H. [3 ]
Wang, Gary Z. [4 ,5 ]
Green, Lisa [3 ]
Goff, Stephen P. [1 ,2 ,6 ]
机构
[1] Columbia Univ, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[2] Columbia Univ, Dept Microbiol & Immunol, New York, NY 10032 USA
[3] Columbia Univ, Dept Biol Sci, New York, NY 10032 USA
[4] Columbia Univ, Med Scientist Training Program, New York, NY 10032 USA
[5] Columbia Univ, Integrated Program Cellular Mol & Biophys Studies, New York, NY 10032 USA
[6] Columbia Univ, Howard Hughes Med Inst, New York, NY 10032 USA
关键词
MURINE LEUKEMIA-VIRUS; NOVO DNA METHYLATION; STEM-CELLS; ENDOGENOUS RETROVIRUSES; TRANSCRIPTION FACTOR; YY1; CHROMATIN; BINDING; EXPRESSION; PROTEIN;
D O I
10.1016/j.celrep.2013.06.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Embryonic cells transcriptionally repress the expression of endogenous and exogenous retroelements. Trim28, a key player in this silencing, is known to act in a large DNA-bound complex, but the other components of the complex are not fully characterized. Here, we show that the zinc finger protein Yin Yang 1 (YY1) is one such component. YY1 binds to the long terminal repeat (LTR) region of both exogenous and endogenous retroviruses (ERVs). Deletion of the YY1-binding site from the retroviral genome leads to a major loss of silencing in embryonic cells and a coordinated loss of repressive histone marks from the proviral chromatin. Depletion of YY1 protein results in marked upregulation of expression of exogenous viruses and of selected ERVs. Finally, we report an embryonic cell-specific interaction between YY1 and Trim28. Our results suggest a major role for YY1 in the silencing of both exogenous retroviruses and ERVs in embryonic cells.
引用
收藏
页码:50 / 58
页数:9
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