Heterochromatin Reorganization during Early Mouse Development Requires a Single-Stranded Noncoding Transcript

被引:77
作者
Casanova, Miguel [1 ,2 ]
Pasternak, Micha [1 ,2 ]
El Marjou, Fatima [1 ,3 ]
Le Baccon, Patricia [1 ,2 ,4 ]
Probst, Aline V. [1 ,2 ]
Almouzni, Genevieve [1 ,2 ]
机构
[1] Inst Curie, Ctr Rech, F-75248 Paris, France
[2] CNRS, UMR218, F-75248 Paris, France
[3] CNRS, UMR144, F-75248 Paris, France
[4] Inst Curie, Ctr Rech, PITC IBiSA Plateforme Imagerie Tissulaire & Cellu, F-75248 Paris, France
关键词
PERICENTRIC HETEROCHROMATIN; CONSTITUTIVE HETEROCHROMATIN; DYNAMIC ORGANIZATION; SATELLITE REPEATS; EPIGENETIC DYNAMICS; LYSINE METHYLATION; CHROMATIN DOMAINS; DNA-REPLICATION; GENE-EXPRESSION; STEM-CELLS;
D O I
10.1016/j.celrep.2013.08.015
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The equalization of pericentric heterochromatin from distinct parental origins following fertilization is essential for genome function and development. The recent implication of noncoding transcripts in this process raises questions regarding the connection between RNA and the nuclear organization of distinct chromatin environments. Our study addresses the interrelationship between replication and transcription of the two parental pericentric heterochromatin (PHC) domains and their reorganization during early embryonic development. We demonstrate that the replication of PHC is dispensable for its clustering at the late two-cell stage. In contrast, using parthenogenetic embryos, we show that pericentric transcripts are essential for this reorganization independent of the chromatin marks associated with the PHC domains. Finally, our discovery that only reverse pericentric transcripts are required for both the nuclear reorganization of PHC and development beyond the two-cell stage challenges current views on heterochromatin organization.
引用
收藏
页码:1156 / 1167
页数:12
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