Literature DB >> 10694754

Oct-4: control of totipotency and germline determination.

M Pesce1, H R Schöler.   

Abstract

The transcription factor Oct-4 is expressed in totipotent embryonic cells and germ cells. As totipotent cells differentiate to form somatic and/or extraembryonic tissues, the Oct-4 gene is downregulated. Primordial germ cells are the only cells in which Oct-4 expression is maintained after postgastrulation. Recent in vivo ablation of the Oct-4 function has shown that the absence of this transcription factor causes early embryonic lethality due to trophectodermal differentiation of cells which normally would give rise to the inner cell mass of the blastocyst. This result strongly suggests that Oct-4 is necessary for the maintenance of the totipotent phenotype of embryonic cells and that this factor likely plays a role as a determinant of the totipotency of germ cells by preventing their differentiation to a somatic cell phenotype during gastrulation. The involvement of Oct-4 in the biology of totipotent and germ cells is here discussed in view of new understanding about Oct-4 function. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10694754     DOI: 10.1002/(SICI)1098-2795(200004)55:4<452::AID-MRD14>3.0.CO;2-S

Source DB:  PubMed          Journal:  Mol Reprod Dev        ISSN: 1040-452X            Impact factor:   2.609


  57 in total

1.  Repression of Ets-2-induced transactivation of the tau interferon promoter by Oct-4.

Authors:  T Ezashi; D Ghosh; R M Roberts
Journal:  Mol Cell Biol       Date:  2001-12       Impact factor: 4.272

2.  Phenotypic complementation establishes requirements for specific POU domain and generic transactivation function of Oct-3/4 in embryonic stem cells.

Authors:  Hitoshi Niwa; Shinji Masui; Ian Chambers; Austin G Smith; Jun-ichi Miyazaki
Journal:  Mol Cell Biol       Date:  2002-03       Impact factor: 4.272

3.  Development and Validation of a Rex1-RFP Potency Activity Reporter Assay That Quantifies Stress-Forced Potency Loss in Mouse Embryonic Stem Cells.

Authors:  Quanwen Li; Nardhy Gomez-Lopez; Sascha Drewlo; Elly Sanchez-Rodriguez; Jing Dai; Elizabeth E Puscheck; Daniel A Rappolee
Journal:  Stem Cells Dev       Date:  2016-01-29       Impact factor: 3.272

4.  High-throughput screen for genes predominantly expressed in the ICM of mouse blastocysts by whole mount in situ hybridization.

Authors:  Toshiyuki Yoshikawa; Yulan Piao; Jinhui Zhong; Ryo Matoba; Mark G Carter; Yuxia Wang; Ilya Goldberg; Minoru S H Ko
Journal:  Gene Expr Patterns       Date:  2005-12-01       Impact factor: 1.224

5.  Subcellular characterization of the primordial germ cell antigen PG2 in adult oocytes.

Authors:  Bernd Püschel; Uta Demus; Christoph Viebahn
Journal:  Histochem Cell Biol       Date:  2005-10-28       Impact factor: 4.304

6.  Differential recruitment of methylated CpG binding domains by the orphan receptor GCNF initiates the repression and silencing of Oct4 expression.

Authors:  Peili Gu; Damien Le Menuet; Arthur C-K Chung; Austin J Cooney
Journal:  Mol Cell Biol       Date:  2006-10-09       Impact factor: 4.272

7.  Production of a monoclonal antibody specific for Pou5f1/Oct4.

Authors:  Tatsuhiko Arakawa; Tomohiko Yoshimi; Masayuki Azuma; Taro Tachibana
Journal:  Monoclon Antib Immunodiagn Immunother       Date:  2013-06

Review 8.  Zebrafish Germ Cell Tumors.

Authors:  Angelica Sanchez; James F Amatruda
Journal:  Adv Exp Med Biol       Date:  2016       Impact factor: 2.622

9.  Skin keratinocytes pre-treated with embryonic stem cell-conditioned medium or BMP4 can be directed to an alternative cell lineage.

Authors:  K L Grinnell; J R Bickenbach
Journal:  Cell Prolif       Date:  2007-10       Impact factor: 6.831

10.  Epigenetic deregulation of the human Oct4 promoter in mouse cells.

Authors:  Young Cha; Min-Kyung Sung; Kyung-Won Jung; Hwan-Hee Kim; Su-Man Lee; Kyung-Soon Park
Journal:  Dev Genes Evol       Date:  2008-09-23       Impact factor: 0.900

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