A Dynamic Role of TBX3 in the Pluripotency Circuitry

Ronan Russell(Universität Ulm), Marcus M. Ilg(Universität Ulm), Qiong Lin(RWTH Aachen University), Guangming Wu(Max Planck Institute for Molecular Biomedicine), André Lechel(Universität Ulm), Wendy Bergmann(Universität Ulm), Tim Eiseler(Universität Ulm), Leonhard Linta(University of Tübingen), Pavan Kumar P(Geisinger Medical Center), Moritz Klingenstein(University of Tübingen), Kenjiro Adachi(Max Planck Institute for Molecular Biomedicine), Meike Hohwieler(Universität Ulm), Olena Sakk, Stefanie Raab(University of Tübingen), Anne Moon(Geisinger Medical Center), Martin Zenke(RWTH Aachen University), Thomas Seufferlein(Universität Ulm), Hans R. Schöler(Max Planck Institute for Molecular Biomedicine), Anett Illing(Universität Ulm), Stefan Liebau(University of Tübingen), Alexander Kleger(Universität Ulm)
Stem Cell Reports
December 1, 2015
Cited by 73Open Access
Full Text

Abstract

Pluripotency represents a cell state comprising a fine-tuned pattern of transcription factor activity required for embryonic stem cell (ESC) self-renewal. TBX3 is the earliest expressed member of the T-box transcription factor family and is involved in maintenance and induction of pluripotency. Hence, TBX3 is believed to be a key member of the pluripotency circuitry, with loss of TBX3 coinciding with loss of pluripotency. We report a dynamic expression of TBX3 in vitro and in vivo using genetic reporter tools tracking TBX3 expression in mouse ESCs (mESCs). Low TBX3 levels are associated with reduced pluripotency, resembling the more mature epiblast. Notably, TBX3-low cells maintain the intrinsic capability to switch to a TBX3-high state and vice versa. Additionally, we show TBX3 to be dispensable for induction and maintenance of naive pluripotency as well as for germ cell development. These data highlight novel facets of TBX3 action in mESCs.


Related Papers

No related papers found

Powered by citation graph analysis