Climate Change Cluster, Faculty of Science, University of Technology Sydney, Ultimo, NSW, Australia.
Department of Biology, University of Konstanz, Konstanz, Germany.
Glob Chang Biol. 2021 Jan;27(2):312-326. doi: 10.1111/gcb.15436. Epub 2020 Nov 16.
Exposure of marine life to low oxygen is accelerating worldwide via climate change and localized pollution. Mass coral bleaching and mortality have recently occurred where reefs have experienced chronic low oxygen events. However, the mechanistic basis of tolerance to oxygen levels inadequate to sustain normal functioning (i.e. hypoxia) and whether it contributes to bleaching susceptibility, remain unknown. We therefore experimentally exposed colonies of the environmentally resilient Acropora tenuis, a common reef-building coral from the Great Barrier Reef, to deoxygenation-reoxygenation stress that was aligned to their natural night-day light cycle. Specifically, the treatment involved removing the 'night-time O buffer' to challenge the inherent hypoxia thresholds. RNA-Seq analysis revealed that coral possess a complete and active hypoxia-inducible factor (HIF)-mediated hypoxia response system (HRS) homologous to other metazoans. As expected, A. tenuis exhibited bleaching resistance and showed a strong inducibility of HIF target genes in response to deoxygenation stress. We applied this same approach in parallel to a colony of Acropora selago, known to be environmnetally susceptible, which conversely exhibited a bleaching phenotype response. This phenotypic divergence of A. selago was accompanied by contrasting gene expression profiles indicative of varied effectiveness of their HIF-HRS. Based on our RNA-Seq analysis, we propose (a) that the HIF-HRS is central for corals to manage deoxygenation stress and (b) that key genes of this system (and the wider gene network) may contribute to variation in coral bleaching susceptibility. Our analysis suggests that heat shock protein (hsp) 70 and 90 are important for low oxygen stress tolerance and further highlights how hsp90 expression might also affect the inducibility of coral HIF-HRS in overcoming a metabolic crisis under deoxygenation stress. We propose that differences in coral HIF-HRS could be central in regulating sensitivity to other climate change stressors-notably thermal stress-that commonly drive bleaching.
海洋生物暴露在低氧环境中的现象正通过气候变化和局部污染在全球范围内加速。最近,在经历慢性低氧事件的珊瑚礁中,大规模珊瑚白化和死亡事件时有发生。然而,对于维持正常功能所需的氧气水平不足(即缺氧)的耐受机制,以及它是否导致白化易感性,仍然未知。因此,我们通过实验将环境弹性强的 A. tenuis 珊瑚的群体暴露于脱氧再氧化应激中,该应激与它们的自然昼夜光照周期相吻合。具体来说,这种处理方法包括去除“夜间 O 缓冲”,以挑战其固有的缺氧阈值。RNA-Seq 分析表明,珊瑚拥有一个完整而活跃的缺氧诱导因子(HIF)介导的缺氧反应系统(HRS),与其他后生动物同源。正如预期的那样,A. tenuis 表现出抗白化能力,并在脱氧应激下强烈诱导 HIF 靶基因。我们将这种方法应用于 A. selago 珊瑚的一个群体,该珊瑚已知对环境敏感,相反,它表现出白化表型反应。A. selago 的这种表型差异伴随着不同有效性的基因表达谱,表明其 HIF-HRS 的差异。基于我们的 RNA-Seq 分析,我们提出(a)HIF-HRS 是珊瑚应对脱氧应激的核心,(b)该系统的关键基因(和更广泛的基因网络)可能有助于珊瑚白化易感性的变化。我们的分析表明,热休克蛋白(hsp)70 和 90 对低氧应激耐受很重要,进一步强调了 hsp90 表达如何影响珊瑚 HIF-HRS 在克服脱氧应激下代谢危机时的诱导能力。我们提出,珊瑚 HIF-HRS 的差异可能是调节对其他气候变化胁迫(特别是热胁迫)敏感性的核心,这些胁迫通常会导致白化。