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Genomic organization and mRNA expression of manganese superoxide dismutase (Mn-SOD) from Hemibarbus mylodon (Teleostei, Cypriniformes)

机译:半边形龙虾锰超氧化物歧化酶(Mn-SOD)的基因组组织和mRNA表达

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The genomic structure of manganese superoxide dismutase (Mn-SOD) was characterized in Hemibarbus mylodon (Teleostei, Cypriniformes), an endangered freshwater fish species, and changes in Mn-SOD mRNA expression in response to various stimuli, such as challenge with lipopolysaccharide (LPS), bacteria, or heavy metals, were examined. H. mylodon Mn-SOD possesses well-conserved features of vertebrate Mn-SODs, including its homologous quinquepartite gene structure (five exons interrupted by four introns) and high sequence identity with vertebrate orthologs in coding regions, including a typical eukaryotic Mn-SOD signature. The 5'-regulatory upstream region of the H. mylodon Mn-SOD gene lacked a canonical TATA sequence; however, it displayed various transcription factor binding elements that may be involved in immune and stress responses, as well as the modulation of enzymes that mediate the metabolism of metals and other xenobiotics. Bioinformatic analysis of Mn-SOD genes from fish and mammalian genome databases revealed chromosomal synteny of the Mn-SOD locus in the vertebrate lineage. Mn-SOD transcripts were ubiquitously detected in diverse tissues with variable levels of basal expression using an RT-PCR assay. Mn-SOD expression in the liver and kidney were significantly modulated by injection of LPS (1, 5, or 10 microg g(-1) body weight), Edwardsiella tarda challenge (5 x 10(3) or 5 x 10(5) cells/fish), and heavy metal exposure (Cd, Cu, or Zn at 5 microM). Results from this study suggest that Mn-SOD plays an important role in the host defence against oxidative damage caused by infection-mediated inflammation and/or toxicant related stress in this species.
机译:锰超氧化物歧化酶(Mn-SOD)的基因组结构在濒危淡水鱼半翅目(Teleostei,Cypriniformes)中得到了表征,并且Mn-SOD mRNA表达随各种刺激(例如脂多糖挑战)而变化。 ),细菌或重金属进行了检查。 H. mylodon Mn-SOD具有脊椎动物Mn-SOD的良好保守特征,包括其同源五倍体基因结构(五个外显子,被四个内含子打断),并与编码区中的脊椎动物直向同源物具有高度序列同一性,包括典型的真核Mn-SOD签名。 H. mylodon Mn-SOD基因的5'调控上游区域缺少规范的TATA序列;然而,它显示出可能与免疫和应激反应以及介导金属和其他异源生物代谢的酶的调节有关的各种转录因子结合元件。来自鱼类和哺乳动物基因组数据库的Mn-SOD基因的生物信息学分析揭示了脊椎动物谱系中Mn-SOD基因座的染色体同构。使用RT-PCR分析法广泛检测到基础表达水平可变的各种组织中的Mn-SOD转录本。通过注射LPS(1、5或10 microg g(-1)体重),爱德华氏菌tarda挑战(5 x 10(3)或5 x 10(5),可以显着调节肝脏和肾脏中Mn-SOD的表达。细胞/鱼类)和重金属暴露(5 microM的Cd,Cu或Zn)。这项研究的结果表明,Mn-SOD在宿主防御由该物种引起的感染介导的炎症和/或与毒性有关的应激引起的氧化损伤中起着重要作用。

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