State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China.
College of Advanced Agricultural Sciences, University of Chinese Academy of Sciences, Beijing 100049, China.
Int J Mol Sci. 2021 Mar 16;22(6):3028. doi: 10.3390/ijms22063028.
Low temperature stress represents a major threat to the lives of both farmed and wild fish species. However, biological pathways determining the development of cold resistance in fish remain largely unknown. Zebrafish larvae at 96 hpf were exposed to lethal cold stress (10 °C) for different time periods to evaluate the adverse effects at organism, tissue and cell levels. Time series RNA sequencing (RNA-seq) experiments were performed to delineate the transcriptomic landscape of zebrafish larvae under cold stress and during the subsequent rewarming phase. The genes regulated by cold stress were characterized by progressively enhanced or decreased expression, whereas the genes associated with rewarming were characterized by rapid upregulation upon return to normal temperature (28 °C). Genes such as , and were identified as the representative molecular markers of cold-induced damages through network analysis. Biological pathways involved in cold stress responses were mined from the transcriptomic data and their functions in regulating cold resistance were validated using specific inhibitors. The autophagy, FoxO and MAPK (mitogen-activated protein kinase) signaling pathways were revealed to be survival pathways for enhancing cold resistance, while apoptosis and necroptosis were the death pathways responsible for cold-induced mortality. Functional mechanisms of the survival-enhancing factors Foxo1, ERK (extracellular signal-regulated kinase) and p38 MAPK were further characterized by inhibiting their activities upon cold stress and analyzing gene expression though RNA-seq. These factors were demonstrated to determine the cold resistance of zebrafish through regulating apoptosis and p53 signaling pathway. These findings have provided novel insights into the stress responses elicited by lethal cold and shed new light on the molecular mechanisms underlying cold resistance of fish.
低温胁迫是养殖和野生鱼类生存的主要威胁之一。然而,鱼类耐寒性形成的生物学途径在很大程度上尚不清楚。本研究以 96 小时pf 期斑马鱼幼鱼为研究对象,采用致死低温胁迫(10℃)处理不同时间,评估其在机体、组织和细胞水平的损伤效应;采用时间序列 RNA 测序(RNA-seq)实验,描绘斑马鱼幼鱼在低温胁迫及随后复温过程中的转录组图谱;采用网络分析鉴定了 、 、 等基因作为冷诱导损伤的代表性分子标记;从转录组数据中挖掘低温胁迫响应的生物学途径,并利用特定抑制剂验证其在调控耐寒性中的作用。研究结果表明,自噬、FoxO 和 MAPK(丝裂原活化蛋白激酶)信号通路是增强鱼类耐寒性的生存途径,而凋亡和坏死则是导致冷诱导死亡的死亡途径。通过抑制冷胁迫下 Foxo1、ERK(细胞外信号调节激酶)和 p38 MAPK 的活性,并通过 RNA-seq 分析基因表达,进一步研究了增强耐寒性的生存因子 Foxo1、ERK 和 p38 MAPK 的功能机制。这些因子通过调节凋亡和 p53 信号通路来决定斑马鱼的耐寒性。本研究为深入理解致死低温引起的应激反应提供了新的见解,为鱼类耐寒性的分子机制研究提供了新的思路。