Transient bursts of Zscan4 expression are accompanied by the rapid derepression of heterochromatin in mouse embryonic stem cells

被引:75
作者
Akiyama, Tomohiko [1 ,2 ]
Xin, Li [2 ]
Oda, Mayumi [1 ]
Sharov, Alexei A. [2 ]
Amano, Misa [2 ]
Piao, Yulan [2 ]
Cadet, J. Scotty [2 ]
Dudekula, Dawood B. [2 ]
Qian, Yong [2 ]
Wang, Weidong [2 ]
Ko, Shigeru B. H. [1 ]
Ko, Minoru S. H. [1 ,2 ]
机构
[1] Keio Univ, Sch Med, Dept Syst Med, Tokyo 160, Japan
[2] NIA, Genet Lab, NIH, Baltimore, MD 21224 USA
基金
美国国家卫生研究院;
关键词
heterochromatin; pericentromere; embryonic stem cells; PREIMPLANTATION DEVELOPMENT; MAMMALIAN TELOMERES; SATELLITE REPEATS; GENE-EXPRESSION; 2-CELL EMBRYOS; GROUND-STATE; ES CELLS; PLURIPOTENT; TRANSCRIPTION; CULTURE;
D O I
10.1093/dnares/dsv013
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mouse embryonic stem cells (mESCs) have a remarkable capacity to maintain normal genome stability and karyotype in culture. We previously showed that infrequent bursts of Zscan4 expression (Z4 events) are important for the maintenance of telomere length and genome stability in mESCs. However, the molecular details of Z4 events remain unclear. Here we show that Z4 events involve unexpected transcriptional derepression in heterochromatin regions that usually remain silent. During a Z4 event, we see rapid derepression and rerepression of heterochromatin leading to a burst of transcription that coincides with transient histone hyperacetylation and DNA demethylation, clustering of pericentromeric heterochromatin around the nucleolus, and accumulation of activating and repressive chromatin remodelling complexes. This heterochromatin-based transcriptional activity suggests that mESCs may maintain their extraordinary genome stability at least in part by transiently resetting their heterochromatin.
引用
收藏
页码:307 / 318
页数:12
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