Brouwer Marius, Larkin Patrick, Brown-Peterson Nancy, King Christina, Manning Steve, Denslow Nancy
Department of Coastal Sciences, University of Southern Mississippi, P.O. Box 7000, Ocean Springs, MS 39566, USA.
Mar Environ Res. 2004 Aug-Dec;58(2-5):787-92. doi: 10.1016/j.marenvres.2004.03.094.
Increases in hypoxic conditions are one of the major factors responsible for declines in estuarine habitat quality, yet to date there are no indicators for recognizing populations of estuarine organisms that are suffering from chronic hypoxic stress. Here we test the hypothesis that alterations in gene and protein expression of antioxidant enzymes and other stress-specific proteins can be used as molecular indicators of hypoxic stress. Blue crabs, Callinectes sapidus, were exposed to 2-3 ppm DO for 5 days. Gene expression was measured using macroarrays constructed from cDNA of 10 partial gene transcripts cloned from blue crab hepatopancreas. Significant (p< or =0.05) down-regulation of gene expression was found for MnSOD, hemocyanin, ribosomal S15 and L23. Subtractive hybridization using RNA from control and hypoxic hepatopancreas tissues also indicated down-regulation of hemocyanin transcription. In contrast, Western blotting showed a significant (p< or =0.05) increase of hemocyanin protein in the hepatopancreas and cross-linking of MnSOD proteins in hypoxia-exposed crabs. Thus, hypoxia-responsive cDNA arrays and Westerns may be useful diagnostic tools for monitoring effects of hypoxia in estuarine crustacea.
缺氧状况的增加是导致河口栖息地质量下降的主要因素之一,但迄今为止,尚无用于识别遭受慢性缺氧应激的河口生物种群的指标。在此,我们检验这样一个假设:抗氧化酶和其他应激特异性蛋白的基因和蛋白表达变化可作为缺氧应激的分子指标。将蓝蟹(Callinectes sapidus)暴露于2 - 3 ppm的溶解氧环境中5天。使用由从蓝蟹肝胰腺克隆的10个部分基因转录本的cDNA构建的宏阵列测量基因表达。发现锰超氧化物歧化酶(MnSOD)、血蓝蛋白、核糖体S15和L23的基因表达有显著(p≤0.05)下调。使用对照和缺氧肝胰腺组织的RNA进行消减杂交也表明血蓝蛋白转录下调。相比之下,蛋白质印迹显示缺氧暴露蟹的肝胰腺中血蓝蛋白显著(p≤0.05)增加,且锰超氧化物歧化酶蛋白发生交联。因此,缺氧反应性cDNA阵列和蛋白质印迹可能是监测河口甲壳类动物缺氧影响的有用诊断工具。