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SPEN is required for Xist upregulation during initiation of X chromosome inactivation.

Teresa Robert-FinestraBeatrice F TanHegias Mira-BontenbalErika TimmersCristina GontanSarra MerzoukBenedetto Daniele GiaimoFrançois DossinWilfred F J Van IJckenJohn W M MartensTilman BorggrefeEdith HeardJoost H Gribnau
Published in: Nature communications (2021)
At initiation of X chromosome inactivation (XCI), Xist is monoallelically upregulated from the future inactive X (Xi) chromosome, overcoming repression by its antisense transcript Tsix. Xist recruits various chromatin remodelers, amongst them SPEN, which are involved in silencing of X-linked genes in cis and establishment of the Xi. Here, we show that SPEN plays an important role in initiation of XCI. Spen null female mouse embryonic stem cells (ESCs) are defective in Xist upregulation upon differentiation. We find that Xist-mediated SPEN recruitment to the Xi chromosome happens very early in XCI, and that SPEN-mediated silencing of the Tsix promoter is required for Xist upregulation. Accordingly, failed Xist upregulation in Spen-/- ESCs can be rescued by concomitant removal of Tsix. These findings indicate that SPEN is not only required for the establishment of the Xi, but is also crucial in initiation of the XCI process.
Keyphrases
  • poor prognosis
  • cell proliferation
  • copy number
  • signaling pathway
  • embryonic stem cells
  • gene expression
  • transcription factor
  • oxidative stress
  • current status
  • rna seq