生理和转录组学分析揭示了模拟运输条件下鳜鱼幼鱼的应激反应、蛋白质合成和代谢重编程的温度依赖调控。

IF 2.5 3区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jinghong He, Bingnan Li, Kexun Chen, Zhiqiang Deng, Sujia Wang, Bo Zhao, Yixiang He
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引用次数: 0

摘要

随着水产养殖长途运输的兴起,温度已成为影响幼鱼生存和健康的关键因素。然而,它们对运输温度的分子适应性尚不清楚。本研究通过生理和转录组学分析,探讨了运输温度对翘嘴鳜幼鱼的影响。以25°C未运输的鱼为对照(C25),建立3个运输温度组:15°C运输(T15)、25°C运输(T25)和30°C运输(T30)。然后在每个转运组与对照组(T15 vs. C25, T25 vs. C25, T30 vs. C25)之间进行比较分析。随着运输温度的升高,肝损伤逐渐加重,在T30达到顶峰,出现明显的水肿和坏死。转录组学分析发现,超过5463个deg和三个WGCNA模块与温度变化显著相关。MEdarkseagreen4模块(T30)中的枢纽基因在溶酶体活性、钙信号和细胞骨架调节中富集,表明破坏细胞稳态是肝损伤的关键驱动因素。在T15时,MEcyan模块富含核糖体功能和脂肪酸代谢中心基因上调,表明低温运输促进了蛋白质合成和能量利用。在T25中,MEpalevioletred3 WGCNA模块中的枢纽基因显示氧化磷酸化和胰岛素信号通路下调,表明能量代谢和生长信号的抑制是应激适应策略的一部分。这些结果加深了我们对常温鱼类在模拟运输过程中温度适应的分子机制的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Physiological and transcriptomic analyses reveal temperature-dependent regulation of stress response, protein synthesis and metabolic reprogramming in juvenile mandarin fish (Siniperca chuatsi) under simulated transport.

With the rise of long-distance transport in aquaculture, temperature has become a key factor affecting juvenile fish survival and health. However, their molecular adaptation to transport temperature is not well understood. In this study, physiological and transcriptomic analyses were conducted to investigate the effects of transport temperatures on juvenile Siniperca chuatsi. With 25 °C non-transported fish as the control (C25), three transport temperature groups were established: transport at 15 °C (T15), transport at 25 °C (T25) and transport at 30 °C (T30). Comparative analyses were then performed between each transport group and the control (T15 vs. C25, T25 vs. C25 and T30 vs. C25). Liver damage became progressively more severe with increasing transport temperature, reaching its peak at T30 with pronounced edema and necrosis. Transcriptomic analysis identified over 5463 DEGs and three WGCNA modules significantly associated with temperature variation. Hub genes in the MEdarkseagreen4 module (T30) were enriched in lysosomal activity, calcium signaling and cytoskeletal regulation, indicating disrupted cellular homeostasis as a key driver of liver damage. At T15, the MEcyan module was enriched with upregulated hub genes for ribosome function and fatty acid metabolism, indicating boosted protein synthesis and energy use under low-temperature transport. In the T25, hub genes in the MEpalevioletred3 WGCNA module showed downregulation of oxidative phosphorylation and insulin signaling pathways, indicating a suppression of energy metabolism and growth signaling as part of a stress-adaptive strategy. These results deepen our understanding of the molecular mechanisms underlying temperature adaptation in eurythermal fish during simulated transport.

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来源期刊
Fish Physiology and Biochemistry
Fish Physiology and Biochemistry 农林科学-生化与分子生物学
CiteScore
5.60
自引率
6.90%
发文量
106
审稿时长
4 months
期刊介绍: Fish Physiology and Biochemistry is an international journal publishing original research papers in all aspects of the physiology and biochemistry of fishes. Coverage includes experimental work in such topics as biochemistry of organisms, organs, tissues and cells; structure of organs, tissues, cells and organelles related to their function; nutritional, osmotic, ionic, respiratory and excretory homeostasis; nerve and muscle physiology; endocrinology; reproductive physiology; energetics; biochemical and physiological effects of toxicants; molecular biology and biotechnology and more.
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