2022
DOI: 10.3389/fmars.2022.962534
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Comparative transcriptome analysis of the differentiating gonads in Scatophagus argus

Abstract: The reproductive-related studies, including genetic and genomic such as gonadal transcriptome analyses, have previously focused on the adult spotted scat, with little information on juvenile fish. Transcriptomics is a powerful tool that allows for massive parallel analysis to identify differential expression and the patterns of gene expression holistically at a particular stage in a cell or tissue development. This study presents the first report on gonadal transcriptome analysis of the differentiating (juveni… Show more

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Cited by 12 publications
(7 citation statements)
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References 109 publications
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“…In addition, the foxl2 can directly bind to the promoter region of the aromatase gene cyp19a1a to promote its expression, or indirectly regulated expression of cyp19a1a through interaction with sf1 (splicing factor 1), resulting in estrogen (E2) production to promote ovarian differentiation ( Wang et al, 2007 ; Zhang et al, 2017 ; Yuan et al, 2021 ). In our present study, folx2 (log2FC = −3.67) and cyp19a1 (log2FC = −6.97) were found to be highly upregulated in the ovary compared with the testis ( Figure 3A ), showing a similar expression pattern to other fish species ( Zhang et al, 2019 ; Mustapha et al, 2022 ). Through a PPI analysis, we found that most of the potential sex-related genes among the DEGs exhibit interaction relationships, suggesting that these genes may play functional roles in sex differentiation and development, potentially being directly or indirectly involved in gonadal development or differentiation.…”
Section: Discussionsupporting
confidence: 76%
“…In addition, the foxl2 can directly bind to the promoter region of the aromatase gene cyp19a1a to promote its expression, or indirectly regulated expression of cyp19a1a through interaction with sf1 (splicing factor 1), resulting in estrogen (E2) production to promote ovarian differentiation ( Wang et al, 2007 ; Zhang et al, 2017 ; Yuan et al, 2021 ). In our present study, folx2 (log2FC = −3.67) and cyp19a1 (log2FC = −6.97) were found to be highly upregulated in the ovary compared with the testis ( Figure 3A ), showing a similar expression pattern to other fish species ( Zhang et al, 2019 ; Mustapha et al, 2022 ). Through a PPI analysis, we found that most of the potential sex-related genes among the DEGs exhibit interaction relationships, suggesting that these genes may play functional roles in sex differentiation and development, potentially being directly or indirectly involved in gonadal development or differentiation.…”
Section: Discussionsupporting
confidence: 76%
“…According to previous similar studies [15,17,18], a total of six mature S. oramin (about one year old) were obtained before spawning (three males and three females) from the waters of Daya Bay, Guangdong Province, in China in May 2023. The temperature of the environment ranged from 27 to 33 • C, with humidity of about 70-80%.…”
Section: Sample Collectionmentioning
confidence: 99%
“…Recently, next-generation sequencing technology has rapidly developed, and transcriptome sequencing technology has been increasingly applied in studies related to fish sex and reproduction. Based on transcriptome sequencing technology, many reproduction-related genes have been uncovered in a large number of fish species, such as yellow catfish (Pleteobagrus fulvidraco) [10], spotted knifejaw (Oplegnathus punctatus) [11], Chinese tongue sole (Cynoglossus semilaevis) [12], silver sillago (Sillago sihama) [13], spot-fin porcupine fish (Diodon hystrix) [14], spotted scat (Scatophagus argus) [15], mandarin fish (Siniperca chuatsi) [16], army fish (Spinibarbus hollandi) [17], white head mandarin fish (Coreoperca whiteheadi) [18], and so on. Based on these reproduction-related genes, researchers can explore their expression and function more pertinently.…”
Section: Introductionmentioning
confidence: 99%
“…The reaction conditions were: predenaturation at 94 • C for 300 s; followed by denaturation at 94 • C for 30 s, annealing at 60 • C for 20 s, and extension at 72 • C for 20 s (fluorescence data acquisition) for 40 cycles. Primer efficiencies were verified in our previous study and ranged from 90% to 105% [18]. Melting curves were checked to confirm the specificity of the PCR amplification.…”
Section: Gene Expression Analysismentioning
confidence: 99%