首页> 外文期刊>Fish & Shellfish Immunology >The molecular characterizations of Cu/ZnSOD and MnSOD and its responses of mRNA expression and enzyme activity to Aeromonas hydrophila or lipopolysaccharide challenge in Qihe crucian carp Carassius auratus
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The molecular characterizations of Cu/ZnSOD and MnSOD and its responses of mRNA expression and enzyme activity to Aeromonas hydrophila or lipopolysaccharide challenge in Qihe crucian carp Carassius auratus

机译:Cu / ZnSOD和MNSOD的分子特征及其对QIHE Crucian Carassius Auratus的AeroMonas患者的MRNA表达和酶活性与酶活性的反应

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Superoxide dismutases (SODs), as the prime antioxidant enzymes, present the first line of defense against oxidative stress caused by excessive reactive oxygen species (ROS) in organism. In the study, two distinct members of SOD family were cloned and analyzed in Qihe crucian carp Carassius auratus (designated as CaCu/ZnSOD and CaMnSOD, respectively). The full-length cDNA of CaCu/ZnSOD is 759 bp, containing a 5'-untranslated region (UTR) of 39 bp, a ORF (including stop codon, TAG) of 465 bp and a 3'-UTR of 255 bp. The ORF of CaCu/ZnSOD encodes a protein of 154 amino acids (aa), in which, two Cu/ZnSOD signature ((45)GFHVHAFGDNT(55) and (139)GNAGGRLACGVI(150)) and four conserved amino acids for Cu/Zn2+-binding sites (H64, H72, H81 and D84) were observed. The full-length CaMnSOD cDNA (960 bp) consists of a 5'-UTR of 114 bp, a ORF of 675 bp and a 3'-UTR of 231 bp, the ORF of CaMnSOD encodes a 224 aa protein with a 26 aa mitochondrial-targeting sequence (MTS) in the N-terminus, and four conserved amino acids for manganese binding (H52, H100, D185 and H189) were observed. Multiple alignment and the structural analysis revealed two Cu/ZnSOD signature motifs and a MnSOD signature motif as well as the invariant binding sites for Cu2+/Zn2+ in CaCu/ZnSOD and Mn2+ in CaMnSOD. The phylogenetic analysis indicated that CaCu/ZnSOD was homologous to cytosolic Cu/ZnSODs, and CaMnSOD was high similarity with mitochondrial MnSODs from other fish. The tissue distribution analysis demonstrated that CaCu/ZnSOD and CaMnSOD were highly expressed in liver, heart and muscle. The dynamic expressions of CaCu/ZnSOD and CaMnSOD were observed after the challenges with Aeromonas hydrophila or LPS, which generally increased in liver, gill, kidney and spleen, while, the mRNA expressions were down regulated at some time points in head kidney. The enzyme activities increased after A. hydrophila or LPS challenge, compared to the control. In this study, the molecular structures and functional motifs of CaCu/ZnSOD and CaMnSOD were determined, and it is crucial for us to understand the biological functions of SODs. The highest level in liver showed that the function of liver to remove ROS is much more important. The obvious responses of mRNA expression levels and enzyme activities to pathogens indicate the important roles of CaCu/ZnSOD and CaMnSOD in antioxidant defense in C auratus. (C) 2017 Elsevier Ltd. All rights reserved.
机译:作为主要抗氧化酶的超氧化物歧化酶(SODS)呈现第一线路防御抗氧化应激因生物体过多的反应性氧(ROS)。在研究中,在齐氏鲫鱼Carassius Auratus(分别被称为CACU / ZNSOD和Camnsod),克隆并分析了两个不同的SOD家族成员。 CACU / ZnSOD的全长cDNA是759bp,含有39bp的5'非翻译区(UTR),ORF(包括止乳封顿,标签)为465bp和255bp的3'-UTR。 CACU / ZnSOD的ORF编码154个氨基酸(AA)的蛋白质,其中,两个Cu / ZnSOD签名((45)GFHVHAFGDNT(55)和(139)Gnagglacgvi(150))和用于Cu /的四个保守氨基酸。 Zn2 + - 桥接位点(H64,H72,H81和D84)被观察到。全长CAMNSOD cDNA(960bp)由114bp的5'-UTR,ORF为675bp和321bp的3'-UTR,CAMNSOD的ORF编码224 AA蛋白,具有26 AA线粒体观察到N-末端中的序列(MTS),并观察到用于锰结合的四个保守的氨基酸(H52,H100,D185和H189)。多对准和结构分析显示了两个Cu / ZnSod标志性主题和MNSOD标记基序以及CACU / ZNSOD和CAMNSOD中的CAC2 + / Zn2 +的不变结合位点。系统发育分析表明,CaCu / ZnSOD对细胞溶质Cu / ZnSODS同源,而Camnsod与来自其他鱼的线粒体MNSODS高相似性。组织分布分析证明了CACU / ZnSOD和Camnsod在肝脏,心脏和肌肉中高度表达。在肝脏,鳃,肾脏和脾脏中通常增加的肝脏,鳃,肾脏和脾脏遭受挑战后观察到CACU / ZnSOD和CAMNSOD的动态表达,而MRNA表达在头肾上的一些时间点下调。与控制相比,酶活性在A.疏水层或LPS挑战后增加。在这项研究中,确定了CaCU / ZnSod和Camnsod的分子结构和功能基序,对于我们了解SODS的生物学功能至关重要。肝脏中最高水平表明,肝脏去除ROS的功能更为重要。 mRNA表达水平和酶活性对病原体的明显反应表明了CACU / ZNSOD和CAMNSOD在C auratus中抗氧化防御中的重要作用。 (c)2017 Elsevier Ltd.保留所有权利。

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