Literature DB >> 35138521

Characterization of the Nanog gene involved in the gonadal development in pearlscale angelfish (Centropyge vrolikii).

Zhaowei Zhong1,2, Yan Xu1,2, Yan Feng1,2, Lulu Ao1,2, Yonghua Jiang3,4.   

Abstract

The homeodomain transcription factor Nanog plays a crucial role in the embryonic and gonadal development and the maintenance of embryonic stem cells (ESCs), interacting with transcription factors such as Oct4 and Sox2 in mammals. Nevertheless, its pathways to molecular mechanisms remain unclear as to teleosts. This study investigates the role of the Nanog gene in gonadal development and sex reversal of pearlscale angelfish (Centropyge vrolikii). To understand the expression pattern of gonadal development, we identified the Nanog gene of C. vrolikii, which we named Cv-Nanog. The full-length cDNA sequence of Cv-Nanog was 2,136 bp in length and encoded a homeodomain protein of 436 amino acid residues. The gene structure and western blot prove results that Cv-Nanog was homologous to the Nanog gene of mammalians. The protein sequence comparison demonstrates that the Cv-Nanog shared a high degree of similarity with orthologs from other vertebrates in the conserved homeodomain. The Cv-Nanog gene was substantially expressed in gonads, and the expression was significantly higher in the ovaries than in the testis, according to quantitative real-time PCR (qRT-PCR) and western blot analyses. In situ hybridization reveals that the transcripts were located in the cytoplasm and membrane of the oocytes in the ovaries and testes. The expression of Cv-Nanog mRNA was weak in Sertoli cells but strong in germ cells. After overexpression of Cv-Nanog, the expression levels of pluripotent factors Sox2 and Oct4 increased significantly with 21.5-fold and 12.2-fold, respectively. Simultaneously, the TGF-beta signaling pathway was activated, and the gonadal cell growth was promoted. The expression of ovary-bias genes Cyp19a and Foxl2 was upregulated, and the expression of testis-bias genes Sox9 and Dmrt1 was downregulated to promote ovarian development. These results imply that the Nanog gene might play a crucial role in the process of gonadal development and sexual reversion in C. vrolikii. This study provides new insight to understand the molecular regulatory mechanism of the Nanog gene further and important clues for the future studies in gonadal development.
© 2022. The Author(s), under exclusive licence to Springer Nature B.V.

Entities:  

Keywords:  Centropyge vrolikii; Nanog; Gonadal development; Gene expression; Sexual reversion

Mesh:

Year:  2022        PMID: 35138521     DOI: 10.1007/s10695-022-01054-8

Source DB:  PubMed          Journal:  Fish Physiol Biochem        ISSN: 0920-1742            Impact factor:   2.794


  47 in total

1.  Functional expression cloning of Nanog, a pluripotency sustaining factor in embryonic stem cells.

Authors:  Ian Chambers; Douglas Colby; Morag Robertson; Jennifer Nichols; Sonia Lee; Susan Tweedie; Austin Smith
Journal:  Cell       Date:  2003-05-30       Impact factor: 41.582

2.  Germ cell restricted expression of chick Nanog.

Authors:  Susana Cañón; Cristina Herranz; Miguel Manzanares
Journal:  Dev Dyn       Date:  2006-10       Impact factor: 3.780

3.  Nanog safeguards pluripotency and mediates germline development.

Authors:  Ian Chambers; Jose Silva; Douglas Colby; Jennifer Nichols; Bianca Nijmeijer; Morag Robertson; Jan Vrana; Ken Jones; Lars Grotewold; Austin Smith
Journal:  Nature       Date:  2007-12-20       Impact factor: 49.962

4.  Multipotent cells can be generated in vitro from several adult human organs (heart, liver, and bone marrow).

Authors:  Antonio P Beltrami; Daniela Cesselli; Natascha Bergamin; Patrizia Marcon; Silvia Rigo; Elisa Puppato; Federica D'Aurizio; Roberto Verardo; Silvano Piazza; Angela Pignatelli; Alessandra Poz; Umberto Baccarani; Daniela Damiani; Renato Fanin; Laura Mariuzzi; Nicoletta Finato; Paola Masolini; Silvia Burelli; Ottorino Belluzzi; Claudio Schneider; Carlo A Beltrami
Journal:  Blood       Date:  2007-05-24       Impact factor: 22.113

5.  KLF4 and PBX1 directly regulate NANOG expression in human embryonic stem cells.

Authors:  Ken Kwok-Keung Chan; Jingyao Zhang; Na-Yu Chia; Yun-Shen Chan; Hui Shan Sim; Ker Sin Tan; Steve Kah-Weng Oh; Huck-Hui Ng; Andre Boon-Hwa Choo
Journal:  Stem Cells       Date:  2009-09       Impact factor: 6.277

6.  Expression of NANOG and NANOGP8 in a variety of undifferentiated and differentiated human cells.

Authors:  Sakthikumar Ambady; Christopher Malcuit; Olga Kashpur; Denis Kole; William F Holmes; Emmett Hedblom; Raymond L Page; Tanja Dominko
Journal:  Int J Dev Biol       Date:  2010       Impact factor: 2.203

7.  Molecular characterization of the human NANOG protein.

Authors:  David F Chang; Steven C Tsai; Xing Chao Wang; Ping Xia; Dinithi Senadheera; Carolyn Lutzko
Journal:  Stem Cells       Date:  2009-04       Impact factor: 6.277

8.  An embryonic stem cell-like gene expression signature in poorly differentiated aggressive human tumors.

Authors:  Ittai Ben-Porath; Matthew W Thomson; Vincent J Carey; Ruping Ge; George W Bell; Aviv Regev; Robert A Weinberg
Journal:  Nat Genet       Date:  2008-05       Impact factor: 38.330

9.  Human STELLAR, NANOG, and GDF3 genes are expressed in pluripotent cells and map to chromosome 12p13, a hotspot for teratocarcinoma.

Authors:  Amander T Clark; Ryan T Rodriguez; Megan S Bodnar; Michael J Abeyta; Marcelle I Cedars; Paul J Turek; Meri T Firpo; Renee A Reijo Pera
Journal:  Stem Cells       Date:  2004       Impact factor: 6.277

10.  Nanog regulates proliferation during early fish development.

Authors:  Esther Camp; Ana V Sánchez-Sánchez; Antonio García-España; Rob Desalle; Lina Odqvist; José Enrique O'Connor; José L Mullor
Journal:  Stem Cells       Date:  2009-09       Impact factor: 6.277

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