A role for non-coding Tsix transcription in partitioning chromatin domains within the mouse X-inactivation centre

被引:29
作者
Navarro, Pablo [1 ]
Chantalat, Sophie [2 ]
Foglio, Mario [2 ]
Chureau, Corinne [1 ]
Vigneau, Sebastien [1 ,3 ]
Clerc, Philippe [1 ]
Avner, Philip [1 ]
Rougeulle, Claire [1 ,4 ]
机构
[1] Inst Pasteur, Unite Genet Mol Murine, URA 2578, F-75724 Paris 15, France
[2] CEA, Inst Genom, Ctr Natl Genotypage, F-91057 Evry, France
[3] Univ Penn, Sch Med, Dept Cell & Dev Biol, Philadelphia, PA 19104 USA
[4] Univ Paris Diderot Paris 7, CNRS, UMR Epigenet & Cell Fat 7216, Paris 13, France
来源
EPIGENETICS & CHROMATIN | 2009年 / 2卷
关键词
EMBRYONIC STEM-CELLS; CHROMOSOME INACTIVATION; HISTONE H3; XIST GENE; RNA; METHYLATION; REPRESSION; ANTISENSE; REPEAT; CHOICE;
D O I
10.1186/1756-8935-2-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Delimiting distinct chromatin domains is essential for temporal and spatial regulation of gene expression. Within the X-inactivation centre region (Xic), the Xist locus, which triggers X-inactivation, is juxtaposed to a large domain of H3K27 trimethylation (H3K27me3). Results: We describe here that developmentally regulated transcription of Tsix, a crucial non-coding antisense to Xist, is required to block the spreading of the H3K27me3 domain to the adjacent H3K4me2-rich Xist region. Analyses of a series of distinct Tsix mutations suggest that the underlying mechanism involves the RNA Polymerase II accumulating at the Tsix 3'-end. Furthermore, we report additional unexpected long-range effects of Tsix on the distal sub-region of the Xic, involved in Xic-Xic trans-interactions. Conclusion: These data point toward a role for transcription of non-coding RNAs as a developmental strategy for the establishment of functionally distinct domains within the mammalian genome.
引用
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页数:15
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