Expression and transcriptional regulation of gsdf in spotted scat (Scatophagus argus)

Gonadal soma-derived factor (Gsdf) is critical for testicular differentiation and early germ cell development in teleosts. The spotted scat (Scatophagus argus), with a stable XX-XY sex-determination system and the candidate sex determination gene dmrt1, provides a good model for understanding the me...

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Veröffentlicht in:Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology 2019-07, Vol.233, p.35-45
Hauptverfasser: Jiang, Dong-Neng, Mustapha, Umar Farouk, Shi, Hong-Juan, Huang, Yuan-Qing, Si-Tu, Jia-Xin, Wang, Mei, Deng, Si-Ping, Chen, Hua-Pu, Tian, Chang-Xu, Zhu, Chun-Hua, Li, Ming-Hui, Li, Guang-Li
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container_title Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology
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creator Jiang, Dong-Neng
Mustapha, Umar Farouk
Shi, Hong-Juan
Huang, Yuan-Qing
Si-Tu, Jia-Xin
Wang, Mei
Deng, Si-Ping
Chen, Hua-Pu
Tian, Chang-Xu
Zhu, Chun-Hua
Li, Ming-Hui
Li, Guang-Li
description Gonadal soma-derived factor (Gsdf) is critical for testicular differentiation and early germ cell development in teleosts. The spotted scat (Scatophagus argus), with a stable XX-XY sex-determination system and the candidate sex determination gene dmrt1, provides a good model for understanding the mechanism of sex determination and differentiation in teleosts. In this study, we analyzed spotted scat gsdf tissue distribution and gene expression patterns in gonads, as well as further analysis of transcriptional regulation. Tissue distribution analysis showed that gsdf was only expressed in testis and ovary. Real-time PCR showed that both gsdf and dmrt1 were expressed significantly higher in testes at different phases (phase III, IV and V) compared to ovaries at phase II, III and IV, while gsdf was expressed significantly higher in phase II ovaries than those of phase III and IV. Western blot analysis also showed that Gsdf was more highly expressed in the testis than ovary. Immunohistochemistry analysis showed that Gsdf was expressed in Sertoli cells surrounding spermatogonia in the testis, while it was expressed in the somatic cells surrounding the oogonia of the ovary. Approximately 2.7 kb of the 5′ upstream region of gsdf was cloned from the spotted scat genomic DNA and in silico promoter analysis revealed the putative transcription factor binding sites of Dmrt1 and Sf1. The luciferase reporter assay, using the human embryonic kidney cells, demonstrated that Dmrt1 activated gsdf expression in a dose-dependent manner in the presence of Sf1 in spotted scat. These results suggest that Gsdf could play a role in regulating the development of spermatogonia and oogonia, and also participate in male sex differentiation by acting as a downstream gene of Dmrt1 in spotted scat. [Display omitted] •Gonadal soma-derived factor (gsdf) was cloned in Scatophagus argus.•Gsdf was more highly expressed in the testes than ovaries in S. argus.•Gsdf is expressed in gonadal somatic cells surrounding spermatozoa and oogonia.•Dmrt1 activates gsdf expression in a dose-dependent manner in the presence of Sf1.
doi_str_mv 10.1016/j.cbpb.2019.04.002
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The spotted scat (Scatophagus argus), with a stable XX-XY sex-determination system and the candidate sex determination gene dmrt1, provides a good model for understanding the mechanism of sex determination and differentiation in teleosts. In this study, we analyzed spotted scat gsdf tissue distribution and gene expression patterns in gonads, as well as further analysis of transcriptional regulation. Tissue distribution analysis showed that gsdf was only expressed in testis and ovary. Real-time PCR showed that both gsdf and dmrt1 were expressed significantly higher in testes at different phases (phase III, IV and V) compared to ovaries at phase II, III and IV, while gsdf was expressed significantly higher in phase II ovaries than those of phase III and IV. Western blot analysis also showed that Gsdf was more highly expressed in the testis than ovary. Immunohistochemistry analysis showed that Gsdf was expressed in Sertoli cells surrounding spermatogonia in the testis, while it was expressed in the somatic cells surrounding the oogonia of the ovary. Approximately 2.7 kb of the 5′ upstream region of gsdf was cloned from the spotted scat genomic DNA and in silico promoter analysis revealed the putative transcription factor binding sites of Dmrt1 and Sf1. The luciferase reporter assay, using the human embryonic kidney cells, demonstrated that Dmrt1 activated gsdf expression in a dose-dependent manner in the presence of Sf1 in spotted scat. These results suggest that Gsdf could play a role in regulating the development of spermatogonia and oogonia, and also participate in male sex differentiation by acting as a downstream gene of Dmrt1 in spotted scat. [Display omitted] •Gonadal soma-derived factor (gsdf) was cloned in Scatophagus argus.•Gsdf was more highly expressed in the testes than ovaries in S. argus.•Gsdf is expressed in gonadal somatic cells surrounding spermatozoa and oogonia.•Dmrt1 activates gsdf expression in a dose-dependent manner in the presence of Sf1.</description><identifier>ISSN: 1096-4959</identifier><identifier>EISSN: 1879-1107</identifier><identifier>DOI: 10.1016/j.cbpb.2019.04.002</identifier><identifier>PMID: 30980893</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Animals ; Dmrt1 ; Female ; Fish Proteins - biosynthesis ; Fish Proteins - genetics ; Gene Expression Regulation - physiology ; Gsdf ; Male ; Ovary - metabolism ; Promoter analysis ; Sex determination and differentiation ; Skates (Fish) - genetics ; Skates (Fish) - metabolism ; Spotted scat (Scatophagus argus) ; Testis - metabolism ; Transcription, Genetic - physiology ; Transforming Growth Factor beta - biosynthesis ; Transforming Growth Factor beta - genetics</subject><ispartof>Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 2019-07, Vol.233, p.35-45</ispartof><rights>2019 Elsevier Inc.</rights><rights>Copyright © 2019 Elsevier Inc. 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The spotted scat (Scatophagus argus), with a stable XX-XY sex-determination system and the candidate sex determination gene dmrt1, provides a good model for understanding the mechanism of sex determination and differentiation in teleosts. In this study, we analyzed spotted scat gsdf tissue distribution and gene expression patterns in gonads, as well as further analysis of transcriptional regulation. Tissue distribution analysis showed that gsdf was only expressed in testis and ovary. Real-time PCR showed that both gsdf and dmrt1 were expressed significantly higher in testes at different phases (phase III, IV and V) compared to ovaries at phase II, III and IV, while gsdf was expressed significantly higher in phase II ovaries than those of phase III and IV. Western blot analysis also showed that Gsdf was more highly expressed in the testis than ovary. Immunohistochemistry analysis showed that Gsdf was expressed in Sertoli cells surrounding spermatogonia in the testis, while it was expressed in the somatic cells surrounding the oogonia of the ovary. Approximately 2.7 kb of the 5′ upstream region of gsdf was cloned from the spotted scat genomic DNA and in silico promoter analysis revealed the putative transcription factor binding sites of Dmrt1 and Sf1. The luciferase reporter assay, using the human embryonic kidney cells, demonstrated that Dmrt1 activated gsdf expression in a dose-dependent manner in the presence of Sf1 in spotted scat. These results suggest that Gsdf could play a role in regulating the development of spermatogonia and oogonia, and also participate in male sex differentiation by acting as a downstream gene of Dmrt1 in spotted scat. [Display omitted] •Gonadal soma-derived factor (gsdf) was cloned in Scatophagus argus.•Gsdf was more highly expressed in the testes than ovaries in S. argus.•Gsdf is expressed in gonadal somatic cells surrounding spermatozoa and oogonia.•Dmrt1 activates gsdf expression in a dose-dependent manner in the presence of Sf1.</description><subject>Animals</subject><subject>Dmrt1</subject><subject>Female</subject><subject>Fish Proteins - biosynthesis</subject><subject>Fish Proteins - genetics</subject><subject>Gene Expression Regulation - physiology</subject><subject>Gsdf</subject><subject>Male</subject><subject>Ovary - metabolism</subject><subject>Promoter analysis</subject><subject>Sex determination and differentiation</subject><subject>Skates (Fish) - genetics</subject><subject>Skates (Fish) - metabolism</subject><subject>Spotted scat (Scatophagus argus)</subject><subject>Testis - metabolism</subject><subject>Transcription, Genetic - physiology</subject><subject>Transforming Growth Factor beta - biosynthesis</subject><subject>Transforming Growth Factor beta - genetics</subject><issn>1096-4959</issn><issn>1879-1107</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1KxDAUhYMozjj6Ai4kS1203qRN2oAbGfwDwYXOOqRpOmbotDVJRd_elBldujn3Jpxz4H4InRNICRB-vUl1NVQpBSJSyFMAeoDmpCxEQggUh3EHwZNcMDFDJ95vALKSZOQYzTIQJZQim6PV3dfgjPe277Dqahyc6rx2dgjxR7XYmfXYqumB-wavfd1g22E_9CGYGnutAr58jdoP72o9eqxc1KtTdNSo1puz_Vyg1f3d2_IxeX55eFrePic6pzQkJVOkyYqcF4yKop6UZAUDanQjMmhy2jCW80pwVlWMVURUXFBQPMbqnOtsgS53vYPrP0bjg9xar03bqs70o5eURgLAWaxdILqzatd770wjB2e3yn1LAnLCKTdywiknnBJyGXHG0MW-f6y2pv6L_PKLhpudwcQrP61x0mtrOm1q64wOsu7tf_0_DjuFqw</recordid><startdate>201907</startdate><enddate>201907</enddate><creator>Jiang, Dong-Neng</creator><creator>Mustapha, Umar Farouk</creator><creator>Shi, Hong-Juan</creator><creator>Huang, Yuan-Qing</creator><creator>Si-Tu, Jia-Xin</creator><creator>Wang, Mei</creator><creator>Deng, Si-Ping</creator><creator>Chen, Hua-Pu</creator><creator>Tian, Chang-Xu</creator><creator>Zhu, Chun-Hua</creator><creator>Li, Ming-Hui</creator><creator>Li, Guang-Li</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201907</creationdate><title>Expression and transcriptional regulation of gsdf in spotted scat (Scatophagus argus)</title><author>Jiang, Dong-Neng ; 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The spotted scat (Scatophagus argus), with a stable XX-XY sex-determination system and the candidate sex determination gene dmrt1, provides a good model for understanding the mechanism of sex determination and differentiation in teleosts. In this study, we analyzed spotted scat gsdf tissue distribution and gene expression patterns in gonads, as well as further analysis of transcriptional regulation. Tissue distribution analysis showed that gsdf was only expressed in testis and ovary. Real-time PCR showed that both gsdf and dmrt1 were expressed significantly higher in testes at different phases (phase III, IV and V) compared to ovaries at phase II, III and IV, while gsdf was expressed significantly higher in phase II ovaries than those of phase III and IV. Western blot analysis also showed that Gsdf was more highly expressed in the testis than ovary. Immunohistochemistry analysis showed that Gsdf was expressed in Sertoli cells surrounding spermatogonia in the testis, while it was expressed in the somatic cells surrounding the oogonia of the ovary. Approximately 2.7 kb of the 5′ upstream region of gsdf was cloned from the spotted scat genomic DNA and in silico promoter analysis revealed the putative transcription factor binding sites of Dmrt1 and Sf1. The luciferase reporter assay, using the human embryonic kidney cells, demonstrated that Dmrt1 activated gsdf expression in a dose-dependent manner in the presence of Sf1 in spotted scat. These results suggest that Gsdf could play a role in regulating the development of spermatogonia and oogonia, and also participate in male sex differentiation by acting as a downstream gene of Dmrt1 in spotted scat. [Display omitted] •Gonadal soma-derived factor (gsdf) was cloned in Scatophagus argus.•Gsdf was more highly expressed in the testes than ovaries in S. argus.•Gsdf is expressed in gonadal somatic cells surrounding spermatozoa and oogonia.•Dmrt1 activates gsdf expression in a dose-dependent manner in the presence of Sf1.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>30980893</pmid><doi>10.1016/j.cbpb.2019.04.002</doi><tpages>11</tpages></addata></record>
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1879-1107
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source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Animals
Dmrt1
Female
Fish Proteins - biosynthesis
Fish Proteins - genetics
Gene Expression Regulation - physiology
Gsdf
Male
Ovary - metabolism
Promoter analysis
Sex determination and differentiation
Skates (Fish) - genetics
Skates (Fish) - metabolism
Spotted scat (Scatophagus argus)
Testis - metabolism
Transcription, Genetic - physiology
Transforming Growth Factor beta - biosynthesis
Transforming Growth Factor beta - genetics
title Expression and transcriptional regulation of gsdf in spotted scat (Scatophagus argus)
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