Zhang Ziping, Ju Zhenlin, Wells Melissa C, Walter Ronald B
Department of Chemistry and Biochemistry, 419 Centennial Hall, Texas State University, 601 University Drive, San Marcos, TX 78666, USA.
J Exp Mar Biol Ecol. 2009 Dec 1;381(Suppl 1):S180-S187. doi: 10.1016/j.jembe.2009.07.021.
Eutrophication leading to hypoxic water conditions has become a major problem in aquatic systems worldwide. Monitoring the levels and biological effects of lowered oxygen levels in aquatic systems may provide data useful in management of natural aquatic environments. Fishes represent an economically important resource that is subject to hypoxia exposure effects. Due to the extreme diversity of fish species and their habitats, fishes in general have evolved unique capabilities to modulate gene expression patterns in response to hypoxic stress. Recent studies have attempted to document quantitative changes in gene expression patterns induced in various fish species in response to reduced dissolved oxygen levels. From a management perspective, the goal of these studies is to provide a more complete characterization of hypoxia responsive genes in fish, as molecular indicators (biomarkers) of ecosystem hypoxic stress.The molecular genetic response to hypoxia is highly complex and overlaps with other stress responses making it difficult to identify hypoxia specific responses using traditional single gene or low throughput approaches. Therefore, recent approaches have been aimed at developing functional genomic (e.g. high density microarray and real-time PCR) and proteomic (two-dimensional fluorescence difference in gel electrophoresis coupled with mass spectrometry based peptide identification) technologies that employ fish species. Many of the fish species utilized in these studies do not have the advantages of underlying genome resources (i.e., genome or transcriptome sequences). Efforts have attempted to establish correlations between discreet molecular responses elicited by fish in response to hypoxia and changes in the genetic profiles of stressed organs or tissues. Notable progress in these areas has been made using several different versions of either cDNA or oligonucleotide based microarrays to profile changes in gene expression patterns in response to hypoxic stress.Due to these efforts, hundreds of hypoxia responsive genes have been identified both from laboratory reared aquaria fish and from feral fish derived from both fresh and saltwater habitats. Herein, we review these reports and the emergence of hypoxia biomarker development in aquatic species. We also include some of our own recent results using the medaka (Oryzias latipes) as a model to define genetic profiles of hypoxia exposure.
富营养化导致水体缺氧已成为全球水生系统中的一个主要问题。监测水生系统中氧含量降低的水平及其生物效应,可能会为自然水生环境的管理提供有用的数据。鱼类是一种具有重要经济价值的资源,容易受到缺氧暴露的影响。由于鱼类物种及其栖息地的极端多样性,一般来说,鱼类已经进化出独特的能力来调节基因表达模式以应对缺氧应激。最近的研究试图记录各种鱼类在溶解氧水平降低时基因表达模式的定量变化。从管理角度来看,这些研究的目标是更全面地表征鱼类中的缺氧反应基因,作为生态系统缺氧应激的分子指标(生物标志物)。对缺氧的分子遗传反应非常复杂,并且与其他应激反应重叠,这使得使用传统的单基因或低通量方法难以识别缺氧特异性反应。因此,最近的方法旨在开发功能基因组学(如高密度微阵列和实时PCR)和蛋白质组学(二维荧光差异凝胶电泳结合基于质谱的肽鉴定)技术,这些技术都应用于鱼类物种。这些研究中使用的许多鱼类物种没有潜在基因组资源(即基因组或转录组序列)的优势。人们努力尝试在鱼类对缺氧引发的离散分子反应与应激器官或组织的基因谱变化之间建立相关性。使用几种不同版本的基于cDNA或寡核苷酸的微阵列来分析缺氧应激下基因表达模式的变化,在这些领域已经取得了显著进展。由于这些努力,已经从实验室饲养的水族箱鱼类以及来自淡水和咸水栖息地的野生鱼类中鉴定出数百个缺氧反应基因。在此,我们综述这些报告以及水生物种中缺氧生物标志物开发的出现情况。我们还包括了我们自己最近使用青鳉(Oryzias latipes)作为模型来定义缺氧暴露基因谱的一些结果。