Epigenetics & Chromatin (Jul 2009)

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

  • Navarro Pablo,
  • Chantalat Sophie,
  • Foglio Mario,
  • Chureau Corinne,
  • Vigneau Sébastien,
  • Clerc Philippe,
  • Avner Philip,
  • Rougeulle Claire

DOI
https://doi.org/10.1186/1756-8935-2-8
Journal volume & issue
Vol. 2, no. 1
p. 8

Abstract

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Abstract 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.