Long Yong, Yan Junjun, Song Guili, Li Xiaohui, Li Xixi, Li Qing, Cui Zongbin
The Key Laboratory of Aquatic Biodiversity and Conservation, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, Hubei, PR China.
University of the Chinese Academy of Sciences, Beijing, PR China.
BMC Genomics. 2015 May 15;16(1):385. doi: 10.1186/s12864-015-1560-y.
Hypoxia and temperature stress are two major adverse environmental conditions often encountered by fishes. The interaction between hypoxia and temperature stresses has been well documented and oxygen is considered to be the limiting factor for the thermal tolerance of fish. Although both high and low temperature stresses can impair the cardiovascular function and the cross-resistance between hypoxia and heat stress has been found, it is not clear whether hypoxia acclimation can protect fish from cold injury.
Pre-acclimation of 96-hpf zebrafish larvae to mild hypoxia (5% O2) significantly improved their resistance to lethal hypoxia (2.5% O2) and increased the survival rate of zebrafish larvae after lethal cold (10°C) exposure. However, pre-acclimation of 96-hpf larvae to cold (18°C) decreased their tolerance to lethal hypoxia although their ability to endure lethal cold increased. RNA-seq analysis identified 132 up-regulated and 41 down-regulated genes upon mild hypoxia exposure. Gene ontology enrichment analyses revealed that genes up-regulated by hypoxia are primarily involved in oxygen transport, oxidation-reduction process, hemoglobin biosynthetic process, erythrocyte development and cellular iron ion homeostasis. Hypoxia-inhibited genes are enriched in inorganic anion transport, sodium ion transport, very long-chain fatty acid biosynthetic process and cytidine deamination. A comparison with the dataset of cold-regulated gene expression identified 23 genes co-induced by hypoxia and cold and these genes are mainly associated with oxidation-reduction process, oxygen transport, hemopoiesis, hemoglobin biosynthetic process and cellular iron ion homeostasis. The alleviation of lipid peroxidation damage by both cold- and hypoxia-acclimation upon lethal cold stress suggests the association of these genes with cold resistance. Furthermore, the alternative promoter of hmbsb gene specifically activated by hypoxia and cold was identified and confirmed.
Acclimation responses to mild hypoxia and cold stress were found in zebrafish larvae and pre-acclimation to hypoxia significantly improved the tolerance of larvae to lethal cold stress. RNA-seq and bioinformatics analyses revealed the biological processes associated with hypoxia acclimation. Transcriptional events co-induced by hypoxia and cold may represent the molecular basis underlying the protection of hypoxia-acclimation against cold injury.
缺氧和温度胁迫是鱼类经常遇到的两种主要不利环境条件。缺氧和温度胁迫之间的相互作用已有充分记载,并且氧气被认为是鱼类热耐受性的限制因素。尽管高温和低温胁迫都会损害心血管功能,并且已经发现缺氧和热应激之间存在交叉抗性,但尚不清楚缺氧适应是否能保护鱼类免受冷损伤。
将96小时胚胎期(hpf)的斑马鱼幼虫预先适应轻度缺氧(5%氧气),可显著提高它们对致死性缺氧(2.5%氧气)的抗性,并提高斑马鱼幼虫在致死性低温(10°C)暴露后的存活率。然而,将96 hpf幼虫预先适应低温(18°C)会降低它们对致死性缺氧的耐受性,尽管它们忍受致死性低温的能力有所提高。RNA测序分析确定了轻度缺氧暴露后132个上调基因和41个下调基因。基因本体富集分析表明,缺氧上调的基因主要参与氧气运输、氧化还原过程、血红蛋白生物合成过程、红细胞发育和细胞铁离子稳态。缺氧抑制的基因富集在无机阴离子运输、钠离子运输、极长链脂肪酸生物合成过程和胞嘧啶脱氨作用中。与冷调节基因表达数据集的比较确定了23个由缺氧和寒冷共同诱导的基因,这些基因主要与氧化还原过程、氧气运输、造血作用、血红蛋白生物合成过程和细胞铁离子稳态相关。在致死性低温胁迫下,冷适应和缺氧适应均减轻了脂质过氧化损伤,这表明这些基因与抗寒能力有关。此外,还鉴定并证实了hmbsb基因的可变启动子在缺氧和寒冷条件下被特异性激活。
在斑马鱼幼虫中发现了对轻度缺氧和冷应激的适应反应,预先适应缺氧可显著提高幼虫对致死性冷应激的耐受性。RNA测序和生物信息学分析揭示了与缺氧适应相关的生物学过程。缺氧和寒冷共同诱导的转录事件可能代表了缺氧适应对冷损伤保护作用的分子基础。