Literature DB >> 15939376

Nanog expression in mouse germ cell development.

Shinpei Yamaguchi1, Hironobu Kimura, Masako Tada, Norio Nakatsuji, Takashi Tada.   

Abstract

Nanog is a newly identified transcriptional factor bearing a homeodomain and expressed in pluripotential cells of preimplantation and early postimplantation embryos, and embryonic stem (ES) and embryonic germ (EG) cells. Knockout experiments indicate that Nanog functions as a key player in maintaining the pluripotency of stem cells. Importantly, Nanog expression is highly expressed in primordial germ cells (PGCs) of E11.5 and E12.5 mouse embryos. However, its temporal and spatial expression pattern and function in germ cells are largely unknown. To address these issues, whole embryos and cryosections of embryos were immunostained with anti-NANOG and anti-STELLA/PGC7 antibodies. NANOG expression, repressed in colonized PGCs of E7.25-E7.5 embryos, became detectable in migrating PGCs of E7.75-E8.0 embryos. Both male and female PGCs migrating in E9.5 and E10.5 embryos and colonizing the genital ridges of E11.5 and E12.5 embryos were positive for NANOG immunostaining, while the NANOG expression pattern differed between the sexes in the later developmental stage. In female gonadal PGCs of E13.5 and E14.5 embryos, NANOG became undetectable in germ cells positive for the synaptonemal complex-specific protein SCP3, while in male PGCs of E14.5-E16.5 embryos, the number of NANOG-positive germ cells drastically decreased during the mitotic arrest. No germ cells positive for NANOG were detectable in testes and ovaries of adult mice. Thus, in germ cell development, NANOG is expressed in proliferating germ cells, in which nuclear reprogramming is progressing.

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Year:  2005        PMID: 15939376     DOI: 10.1016/j.modgep.2005.03.001

Source DB:  PubMed          Journal:  Gene Expr Patterns        ISSN: 1567-133X            Impact factor:   1.224


  90 in total

1.  NANOG regulates glioma stem cells and is essential in vivo acting in a cross-functional network with GLI1 and p53.

Authors:  Marie Zbinden; Arnaud Duquet; Aiala Lorente-Trigos; Sandra-Nadia Ngwabyt; Isabel Borges; Ariel Ruiz i Altaba
Journal:  EMBO J       Date:  2010-06-25       Impact factor: 11.598

2.  NANOG induction of fetal liver kinase-1 (FLK1) transcription regulates endothelial cell proliferation and angiogenesis.

Authors:  Erin E Kohler; Colleen E Cowan; Ishita Chatterjee; Asrar B Malik; Kishore K Wary
Journal:  Blood       Date:  2010-11-30       Impact factor: 22.113

3.  Zebrafish models of germ cell tumor.

Authors:  Joanie C Neumann; Kate Lillard; Vanessa Damoulis; James F Amatruda
Journal:  Methods Cell Biol       Date:  2011       Impact factor: 1.441

Review 4.  Zebrafish Germ Cell Tumors.

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

5.  Misexpression of cyclin D1 in embryonic germ cells promotes testicular teratoma initiation.

Authors:  Denise G Lanza; Emily P Dawson; Priya Rao; Jason D Heaney
Journal:  Cell Cycle       Date:  2016-02-22       Impact factor: 4.534

Review 6.  Pluripotency of male germline stem cells.

Authors:  Sungtae Kim; Juan Carlos Izpisua Belmonte
Journal:  Mol Cells       Date:  2011-03-24       Impact factor: 5.034

Review 7.  Testicular germ cell tumours: predisposition genes and the male germ cell niche.

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Journal:  Nat Rev Cancer       Date:  2011-03-17       Impact factor: 60.716

Review 8.  Switching on pluripotency: a perspective on the biological requirement of Nanog.

Authors:  Thorold W Theunissen; José C R Silva
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2011-08-12       Impact factor: 6.237

Review 9.  SWI/SNF chromatin remodeling complex: a new cofactor in reprogramming.

Authors:  Ling He; Huan Liu; Liling Tang
Journal:  Stem Cell Rev Rep       Date:  2012-03       Impact factor: 5.739

Review 10.  The stem cell identity of testicular cancer.

Authors:  Amander T Clark
Journal:  Stem Cell Rev       Date:  2007-01       Impact factor: 5.739

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