{"title":"Comparative Transcriptomic Analysis of Prefertilization Stage V Testes and Ovaries in Hemibagrus guttatus","authors":"Lan Ma, Zuoyu Jiang, Wei Xiong, Junjie Yao, Julin Wang, Xianjun Zhou, Guotao Yan, Xianyi Mo, Jiwei Chen, Zhengqi Liang","doi":"10.1155/are/4873171","DOIUrl":null,"url":null,"abstract":"<p>To investigate the gene expression characteristics associated with stage V gonadal development in <i>Hemibagrus guttatus</i>, transcriptome sequencing was performed on stage V testes and ovaries using an Illumina high-throughput sequencing platform. In total, 97,689 unigenes were obtained after de novo assembly; a total of 5364 differentially expressed genes (DEGs) were identified between testes and ovaries samples. Compared with the testes, 2518 genes (46.9%) were upregulated and 2846 genes (53.1%) were downregulated in the ovaries. Combined with Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses, 80 key DEGs related to gonadal development were further screened out, among which 44 were highly expressed in testes and 36 were highly expressed in ovaries. These DEGs were mainly enriched in 21 signaling pathways regulating sex determination, differentiation, and gonadal development, including steroid hormone biosynthesis, gonadotropin regulation, the TGF-β pathway, and progesterone-mediated oocyte maturation. These results indicate that multiple genes involved in hormone synthesis, gamete maturation, and energy and substance metabolism exhibit significant sex-biased expression in stage V testes and ovaries of <i>H. guttatus</i>, which may collectively provide the endocrine environment and the material and energy reserves required for subsequent fertilization.</p>","PeriodicalId":8104,"journal":{"name":"Aquaculture Research","volume":"2026 1","pages":""},"PeriodicalIF":2.5000,"publicationDate":"2026-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/are/4873171","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aquaculture Research","FirstCategoryId":"97","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1155/are/4873171","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0
Abstract
To investigate the gene expression characteristics associated with stage V gonadal development in Hemibagrus guttatus, transcriptome sequencing was performed on stage V testes and ovaries using an Illumina high-throughput sequencing platform. In total, 97,689 unigenes were obtained after de novo assembly; a total of 5364 differentially expressed genes (DEGs) were identified between testes and ovaries samples. Compared with the testes, 2518 genes (46.9%) were upregulated and 2846 genes (53.1%) were downregulated in the ovaries. Combined with Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses, 80 key DEGs related to gonadal development were further screened out, among which 44 were highly expressed in testes and 36 were highly expressed in ovaries. These DEGs were mainly enriched in 21 signaling pathways regulating sex determination, differentiation, and gonadal development, including steroid hormone biosynthesis, gonadotropin regulation, the TGF-β pathway, and progesterone-mediated oocyte maturation. These results indicate that multiple genes involved in hormone synthesis, gamete maturation, and energy and substance metabolism exhibit significant sex-biased expression in stage V testes and ovaries of H. guttatus, which may collectively provide the endocrine environment and the material and energy reserves required for subsequent fertilization.
期刊介绍:
International in perspective, Aquaculture Research is published 12 times a year and specifically addresses research and reference needs of all working and studying within the many varied areas of aquaculture. The Journal regularly publishes papers on applied or scientific research relevant to freshwater, brackish, and marine aquaculture. It covers all aquatic organisms, floristic and faunistic, related directly or indirectly to human consumption. The journal also includes review articles, short communications and technical papers. Young scientists are particularly encouraged to submit short communications based on their own research.