Characterization of the Nanog gene involved in the gonadal development in pearlscale angelfish (Centropyge vrolikii)
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 t...
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Veröffentlicht in: | Fish physiology and biochemistry 2022-04, Vol.48 (2), p.303-319 |
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Zusammenfassung: | 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. |
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ISSN: | 0920-1742 1573-5168 |
DOI: | 10.1007/s10695-022-01054-8 |