@article{MuenstThierWinnemoelleretal.2016,
  author    = {M{\"u}nst, Bernhard and Thier, Marc Christian and Winnem{\"o}ller, Dirk and Helfen, Martina and Thummer, Rajkumar P. and Edenhofer, Frank},
  title     = {Nanog induces suppression of senescence through downregulation of p27\(^{KIP1}\) expression},
  series = {Journal of Cell Science},
  volume    = {129},
  journal   = {Journal of Cell Science},
  number    = {5},
  doi       = {10.1242/jcs.167932},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-190761},
  pages     = {912-920},
  year      = {2016},
  abstract  = {A comprehensive analysis of the molecular network of cellular factors establishing and maintaining pluripotency as well as self renewal of pluripotent stem cells is key for further progress in understanding basic stem cell biology. Nanog is necessary for the natural induction of pluripotency in early mammalian development but dispensable for both its maintenance and its artificial induction. To gain further insight into the molecular activity of Nanog, we analyzed the outcomes of Nanog gain-of-function in various cell models employing a recently developed biologically active recombinant cell-permeant protein, Nanog-TAT. We found that Nanog enhances the proliferation of both NIH 3T3 and primary fibroblast cells. Nanog transduction into primary fibroblasts results in suppression of senescence-associated beta-galactosidase activity. Investigation of cell cycle factors revealed that transient activation of Nanog correlates with consistent downregulation of the cell cycle inhibitor p27\(^{KIP1}\) (also known as CDKN1B). By performing chromatin immunoprecipitation analysis, we confirmed bona fide Nanog-binding sites upstream of the p27\(^{KIP1}\) gene, establishing a direct link between physical occupancy and functional regulation. Our data demonstrates that Nanog enhances proliferation of fibroblasts through transcriptional regulation of cell cycle inhibitor p27 gene.},
  language  = {en}
}