Comparative transcriptome analysis identified genes involved in ovarian development in Takifugu rubripes

被引:0
|
作者
Hu, Mingtao [1 ,2 ,4 ]
Yan, Hongwei [1 ,2 ,4 ]
Chen, Jinfeng [1 ,3 ,4 ]
Gao, Rui [1 ,3 ,4 ]
Li, Weiyuan [2 ]
Zhou, Huiting [1 ,2 ,4 ]
Wang, Jia [1 ,2 ,4 ]
Liu, Qi [1 ,3 ,4 ]
Wang, Xiuli [2 ,4 ]
Hu, Pengfei [5 ]
Fu, Chuang [6 ]
机构
[1] Dalian Ocean Univ, Key Lab Environm Controlled Aquaculture, Minist Educ, Dalian 116023, Peoples R China
[2] Dalian Ocean Univ, Coll Fisheries & Life Sci, Dalian 116023, Peoples R China
[3] Dalian Ocean Univ, Coll Marine Sci & Environm Engn, Dalian 116023, Liaoning, Peoples R China
[4] Dalian Ocean Univ, Key Lab Pufferfish Breeding & Culture Liaoning Pro, Dalian 116023, Liaoning, Peoples R China
[5] Inner Mongolia Agr & Anim Husb Technol Promot Ctr, Inner Mongolia 015199, Peoples R China
[6] Changhai Cty Marine & Fisheries Comprehens Adm Law, Dalian, Peoples R China
关键词
Takifugu rubripes; RNA-Seq; Ovary and ovarian development; TIGER PUFFER; MOLECULAR-CLONING; ZONA-PELLUCIDA; EXPRESSION; FOXL2; MATURATION; HORMONE; GROWTH; FISH; DIFFERENTIATION;
D O I
10.1016/j.cbd.2024.101407
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ovarian development is a complex process involving multiple genes, but the molecular mechanisms underlying this process in Takifugu rubripes remain poorly understood. This study aimed to identify genes associated with ovarian development in T. rubripes and to investigate the regulatory mechanisms of oocyte maturation. Transcriptome data were compared across four different developmental stages (stage II to V) to identify differentially expressed genes (DEGs) and perform GO and KEGG enrichment analysis. The expression patterns of randomly selected genes were then validated by qPCR. The results yielded a total of 1,289,401,820 raw data from all libraries, with 16,929 DEGs identified across all comparison groups. The DEGs were predominantly enriched in ovarian steroidogenesis, estrogen-mediated signaling, and TGF-beta signaling pathways. The qPCR analysis showed that cyp17a1 was identified as being expressed at similar levels in stage II and III. Thereafter, cyp17a1 was observed to undergo a continuous increase in expression from stage III to V. cyp19a1, nanos1, foxl2 and ar were identified as being expressed at similar levels at stage II and III, then increase in expression from stage III to IV and subsequent downregulation from stage IV to V. hsd17b1 was identified as being expressed at similar levels at stage II and IV. This study represents a transcriptomic study of ovarian development in female T. rubripes. Several essential ovarian-related genes and sex-related biological pathways were identified. The results will improve our understanding of the molecular mechanisms underlying ovarian development in this species.
引用
收藏
页数:16
相关论文
共 50 条
  • [1] Comparative transcriptome analysis identified genes involved in testicular development in Takifugu rubripes
    Chen, Jinfeng
    Hu, Mingtao
    Li, Meiyuan
    Wang, Chenqi
    Wang, Liu
    Tian, Yushun
    Yan, Hongwei
    Liu, Qi
    Liang, Xinyan
    Wang, Xiuli
    FISH PHYSIOLOGY AND BIOCHEMISTRY, 2025, 51 (01)
  • [2] Comparative transcriptome analysis of fast twitch muscle and slow twitch muscle in Takifugu rubripes
    Gao, Kailun
    Wang, Zhicheng
    Zhou, Xiaoxu
    Wang, Haoze
    Kong, Derong
    Jiang, Chen
    Wang, Xiuli
    Jiang, Zhiqiang
    Qiu, Xuemei
    COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY D-GENOMICS & PROTEOMICS, 2017, 24 : 79 - 88
  • [3] Comparative transcriptome analysis identified candidate genes involved in mycelium browning in Lentinula edodes
    Seung-il Yoo
    Hwa-Yong Lee
    Kesavan Markkandan
    Suyun Moon
    Yong Ju Ahn
    Sumin Ji
    Junsu Ko
    Seong-Jin Kim
    Hojin Ryu
    Chang Pyo Hong
    BMC Genomics, 20
  • [4] Comparative transcriptome analysis identified candidate genes involved in mycelium browning in Lentinula edodes
    Yoo, Seung-il
    Lee, Hwa-Yong
    Markkandan, Kesavan
    Moon, Suyun
    Ahn, Yong Ju
    Ji, Sumin
    Ko, Junsu
    Kim, Seong-Jin
    Ryu, Hojin
    Hong, Chang Pyo
    BMC GENOMICS, 2019, 20 (1)
  • [5] Comparative transcriptome profiling and functional analysis in the blood of tiger puffer (Takifugu rubripes) in response to acute hypoxia
    Lu, Yun
    Li, Yan
    Bao, Mingxiu
    Shang, Fengqin
    Wei, Renjie
    Liu, Fujun
    Liu, Yang
    Wang, Xiuli
    AQUACULTURE REPORTS, 2023, 30
  • [6] Comparative RNA-Seq analysis of differentially expressed genes in the testis and ovary of Takifugu rubripes
    Wang, Zhicheng
    Qiu, Xuemei
    Kong, Derong
    Zhou, Xiaoxu
    Guo, Zhongbao
    Gao, Changfu
    Ma, Shuai
    Hao, Weiwei
    Jiang, Zhiqiang
    Liu, Shengcong
    Zhang, Tao
    Meng, Xuesong
    Wang, Xiuli
    COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY D-GENOMICS & PROTEOMICS, 2017, 22 : 50 - 57
  • [7] Transcriptomic analysis reveals the genes involved in tetrodotoxin (TTX) accumulation, translocation, and detoxification in the pufferfish Takifugu rubripes
    Zhang, Hanyuan
    Li, Peizhen
    Wu, Biyin
    Hou, Jilun
    Ren, Jiangong
    Zhu, Youxiu
    Xu, Jian
    Si, Fei
    Sun, Zhaohui
    Liu, Xia
    CHEMOSPHERE, 2022, 303
  • [8] Comparative transcriptome analysis reveals genes involved in trichome development and metabolism in tobacco
    Chen, Mingli
    Li, Zhiyuan
    He, Xinxi
    Zhang, Zhe
    Wang, Dong
    Cui, Luying
    Xie, Minmin
    Zhao, Zeyu
    Sun, Quan
    Wang, Dahai
    Dai, Jiameng
    Gong, Daping
    BMC PLANT BIOLOGY, 2024, 24 (01):
  • [9] Transcriptome analysis of the gill of Takifugu rubripes using Illumina sequencing for discovery of SNPs
    Cui, Jun
    Wang, Hongdi
    Liu, Shikai
    Qiu, Xuemei
    Jiang, Zhiqiang
    Wang, Xiuli
    COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY D-GENOMICS & PROTEOMICS, 2014, 10 : 44 - 51
  • [10] Retinal development and the expression profiles of opsin genes during larval development in Takifugu rubripes
    Zhang, Qi
    Wu, Yumeng
    Li, Weiyuan
    Wang, Jia
    Zhou, Huiting
    Zhang, Lei
    Liu, Qi
    Ying, Liu
    Yan, Hongwei
    JOURNAL OF FISH BIOLOGY, 2023, 102 (02) : 380 - 394