Chen Jinfeng, Hu Mingtao, Li Meiyuan, Wang Chenqi, Wang Liu, Tian Yushun, Yan Hongwei, Liu Qi, Liang Xinyan, Wang Xiuli
Key Laboratory of Environment Controlled Aquaculture (Dalian Ocean University), Ministry of Education, Dalian, 116023, China.
College of Marine Science and Environment Engineering, Dalian Ocean University, Dalian, 116023, China.
Fish Physiol Biochem. 2025 Jan 6;51(1):2. doi: 10.1007/s10695-024-01439-x.
To identify candidate genes and pathways involved in testicular development in Takifugu rubripes, a comparative transcription analysis was conducted across the various developmental stages of the testis (stages II to V). A total of 9520 differentially expressed genes (DEGs) were identified among the different stages, and they were significantly clustered into six clusters (P < 0.05). One thousand four hundred eleven DEGs such as gndf, wnt1, and cyp17b1 were found to be decreased from stage II to V. In contrast, 994 DEGs such as fn1, ift81, and cdc25a were found to be increased from stage II to V. Six thousand three hundred eighteen DEGs (e.g., dmrt1, sdk2, and chrna1) were identified as being expressed at similar levels at stages II and III. However, they were subsequently found to be decreased from stage III to IV. Four hundred one DEGs exhibited a significant upregulation trend from stage II to III. These genes were expressed at similar levels in stages III, IV, and V, including chrnd, wnt4a, and cyp7a1. The highest expression levels of 200 DEGs (e.g., ccnb2, cdk1, and sycp2) were observed in stage IV, while 196 DEGs (e.g., chmp1b, hsd17b3, and zp3) exhibited the highest expression level in stage III. Those DEGs were mainly enriched in the pathways (e.g., neuroactive ligand-receptor interaction, cell adhesion molecules, and calcium signaling pathways) associated with testicular development. Quantitative polymerase chain reaction of eight randomly selected genes validated the RNA sequencing results. This study may provide new insights into the molecular regulatory mechanisms governing testicular development and spermatogenesis in T. rubripes.
为了鉴定参与红鳍东方鲀睾丸发育的候选基因和信号通路,对睾丸的不同发育阶段(II至V期)进行了比较转录分析。在不同阶段共鉴定出9520个差异表达基因(DEG),它们显著聚为六个簇(P < 0.05)。发现1411个DEG(如gndf、wnt1和cyp17b1)从II期到V期表达量下降。相反,994个DEG(如fn1、ift81和cdc25a)从II期到V期表达量增加。6318个DEG(如dmrt1、sdk2和chrna1)在II期和III期表达水平相似,但随后发现从III期到IV期表达量下降。401个DEG从II期到III期呈现显著上调趋势,这些基因在III期、IV期和V期表达水平相似,包括chrnd、wnt4a和cyp7a1。200个DEG(如ccnb2、cdk1和sycp2)在IV期表达水平最高,而196个DEG(如chmp1b、hsd17b3和zp3)在III期表达水平最高。这些DEG主要富集在与睾丸发育相关的信号通路(如神经活性配体-受体相互作用、细胞粘附分子和钙信号通路)中。对八个随机选择基因的定量聚合酶链反应验证了RNA测序结果。本研究可能为红鳍东方鲀睾丸发育和精子发生的分子调控机制提供新的见解。