Evidence map›Paper›PMID 39244546›Full record

ArticleBiology of sex differences2024

Histological observations and transcriptome analyses reveal the dynamic changes in the gonads of the blotched snakehead (Channa maculata) during sex differentiation and gametogenesis.

Xiaotian Zhang, Yuxia Wu, Yang Zhang, Jin Zhang, Pengfei Chu, Kunci Chen, Haiyang Liu, Qing Luo, Shuzhan Fei, Jian Zhao and 1 more

Abstract read
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Article in Biology of sex differences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Molecular Characterization and Functional Analysis ofInternational journal of molecular sciences · 2026
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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Xiaotian ZhangKey Laboratory of Tropical and Subtropical Fishery Resources Application and Cultivation, Ministry of Agriculture and Rural Affairs, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, No. 1 Xingyu Road, Xilang, Liwan District, Guangzhou, 510380, Guangdong, China.
Yuxia WuKey Laboratory of Tropical and Subtropical Fishery Resources Application and Cultivation, Ministry of Agriculture and Rural Affairs, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, No. 1 Xingyu Road, Xilang, Liwan District, Guangzhou, 510380, Guangdong, China.
Yang ZhangKey Laboratory of Tropical and Subtropical Fishery Resources Application and Cultivation, Ministry of Agriculture and Rural Affairs, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, No. 1 Xingyu Road, Xilang, Liwan District, Guangzhou, 510380, Guangdong, China.
Jin ZhangKey Laboratory of Tropical and Subtropical Fishery Resources Application and Cultivation, Ministry of Agriculture and Rural Affairs, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, No. 1 Xingyu Road, Xilang, Liwan District, Guangzhou, 510380, Guangdong, China.
Pengfei ChuCollege of Animal Science and Technology, Yangzhou University, Yangzhou, 225000, China.
Kunci ChenKey Laboratory of Tropical and Subtropical Fishery Resources Application and Cultivation, Ministry of Agriculture and Rural Affairs, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, No. 1 Xingyu Road, Xilang, Liwan District, Guangzhou, 510380, Guangdong, China.
Haiyang LiuKey Laboratory of Tropical and Subtropical Fishery Resources Application and Cultivation, Ministry of Agriculture and Rural Affairs, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, No. 1 Xingyu Road, Xilang, Liwan District, Guangzhou, 510380, Guangdong, China.
Qing LuoKey Laboratory of Tropical and Subtropical Fishery Resources Application and Cultivation, Ministry of Agriculture and Rural Affairs, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, No. 1 Xingyu Road, Xilang, Liwan District, Guangzhou, 510380, Guangdong, China.
Shuzhan FeiKey Laboratory of Tropical and Subtropical Fishery Resources Application and Cultivation, Ministry of Agriculture and Rural Affairs, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, No. 1 Xingyu Road, Xilang, Liwan District, Guangzhou, 510380, Guangdong, China.
Jian ZhaoKey Laboratory of Tropical and Subtropical Fishery Resources Application and Cultivation, Ministry of Agriculture and Rural Affairs, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, No. 1 Xingyu Road, Xilang, Liwan District, Guangzhou, 510380, Guangdong, China. zhaojian@prfri.ac.cn.
Mi OuKey Laboratory of Tropical and Subtropical Fishery Resources Application and Cultivation, Ministry of Agriculture and Rural Affairs, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, No. 1 Xingyu Road, Xilang, Liwan District, Guangzhou, 510380, Guangdong, China. om1990@prfri.ac.cn.

Funding

Basic and Applied Basic Research Foundation of Guangdong Province 2024A1515030165Central Public-interest Scientific Institution Basal Research Fund, Chinese Academy of Fishery Sciences 2023TD37Central Public-interest Scientific Institution Basal Research Fund, Chinese Academy of Fishery Sciences 2023XT0202China Agriculture Research System of MOF and MARA CARS-46China-ASEAN Maritime Cooperation Fund CAMC-2018FGuangdong Province Rural Revitalization Strategy Special Fund 2022-SPY-00-016National Natural Science Foundation of China 32373127
6 · The paper itself

Abstract

backgroundBlotched snakehead (Channa maculata) displays significant sexual dimorphism, with males exhibiting faster growth rates and larger body sizes compared to females. The cultivation of the all-male population of snakeheads holds substantial economic and ecological value. Nonetheless, the intricate processes governing the development of bipotential gonads into either testis or ovary in C. maculata remain inadequately elucidated. Therefore, it is necessary to determine the critical time window of sex differentiation in C. maculata, providing a theoretical basis for sex control in production practices.

methodsThe body length and weight of male and female C. maculata were measured at different developmental stages to reveal when sexual dimorphism in growth initially appears. Histological observations and spatiotemporal comparative transcriptome analyses were performed on ovaries and testes across various developmental stages to determine the crucial time windows for sex differentiation in each sex and the sex-related genes. Additionally, qPCR and MG2C were utilized to validate and locate sex-related genes, and levels of E

resultsSexual dimorphism in growth became evident starting from 90 dpf. Histological observations revealed that morphological sex differentiation in females and males occurred between 20 and 25 dpf or earlier and 30-35 dpf or earlier, respectively, corresponding to the appearance of the ovarian cavity or efferent duct anlage. Transcriptome analyses revealed divergent gene expression patterns in testes and ovaries after 30 dpf. The periods of 40-60 dpf and 60-90 dpf marked the initiation of molecular sex differentiation in females and males, respectively. Male-biased genes (Sox11a, Dmrt1, Amh, Amhr2, Gsdf, Ar, Cyp17a2) likely play crucial roles in male sex differentiation and spermatogenesis, while female-biased genes (Foxl2, Cyp19a1a, Bmp15, Figla, Er) could be pivotal in ovarian differentiation and development. Numerous biological pathways linked to sex differentiation and gametogenesis were also identified. Additionally, E

conclusionsThis study provides a comprehensive overview of gonadal dynamic changes during sex differentiation and gametogenesis in C. maculata, establishing a scientific foundation for sex control in this species.

Indexed as

GametogenesisSex CharacteristicsSex DifferentiationAnimalsChanna punctataFemaleFishesGene Expression ProfilingGene Expression Regulation, DevelopmentalGonadsMaleOvaryTestisTranscriptomeChanna maculataGametogenesisSex differentiationSexual dimorphism

Identifiers

PMID39244546
PMCPMC11380785

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