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First published online September 7, 2007
doi: 10.1242/10.1242/dev.006569

1 Institut de Génomique Fonctionnelle de Lyon, Université de Lyon,
Université Lyon 1, CNRS, INRA, Ecole Normale Supérieure de Lyon,
France.
2 Department of Anatomy and Developmental Biology, University College London,
London, UK.
3 Roslin Institute, Roslin, Midlothian EH25 9PS, UK.
4 Inserm, U384, Faculté de Médecine, 28, place Henri Dunant,
Clermont-Ferrand, F-63001, France.
5 Département de Physiologie Animale, INRA, France.
Author for correspondence (e-mail:
bepain{at}u-clermont1.fr)
Accepted 16 July 2007
Embryonic stem cells (ESC) have been isolated from pregastrulation mammalian embryos. The maintenance of their pluripotency and ability to self-renew has been shown to be governed by the transcription factors Oct4 (Pou5f1) and Nanog. Oct4 appears to control cell-fate decisions of ESC in vitro and the choice between embryonic and trophectoderm cell fates in vivo. In non-mammalian vertebrates, the existence and functions of these factors are still under debate, although the identification of the zebrafish pou2 (spg; pou5f1) and Xenopus Pou91 (XlPou91) genes, which have important roles in maintaining uncommitted putative stem cell populations during early development, has suggested that these factors have common functions in all vertebrates. Using chicken ESC (cESC), which display similar properties of pluripotency and long-term self-renewal to mammalian ESC, we demonstrated the existence of an avian homologue of Oct4 that we call chicken PouV (cPouV). We established that cPouV and the chicken Nanog gene are required for the maintenance of pluripotency and self-renewal of cESC. These findings show that the mechanisms by which Oct4 and Nanog regulate pluripotency and self-renewal are not exclusive to mammals.
Key words: Nanog, Oct4, Avian homologue, cPouV, Stem cells
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