斑节对虾含硒谷胱甘肽过氧化物酶基因全长克隆及表达分析
作者:
作者单位:

华南农业大学动物科学学院,中国水产科学研究院南海水产研究所,中国水产科学研究院南海水产研究所,中国水产科学研究院南海水产研究所,中国水产科学研究院南海水产研究所,华南农业大学动物科学学院,中国水产科学研究院南海水产研究所

作者简介:

通讯作者:

中图分类号:

基金项目:

现代农业产业技术体系建设专项(CARS-47);广东省科技计划项目(2014B020202003);海南省应用技术研发与示范推广专项(ZDXM2015056);深圳市生物产业发展专项资金现代农业生物产业推广扶持计划(NYSW20140331010053)


Full-length cDNA cloning and expression analysis of selenium-dependent glutathione peroxidase from Penaeus monodon
Author:
Affiliation:

College of Animal Science,South China Agricultural University,South China Sea Fisheries Research Institute,Chinese Academy of Fishery Sciences,,,,,Key Lab. of South China Sea Fishery Resources Exploitation & Utilization,Ministry of Agriculture; South China Sea Fisheries Research Institute,Chinese Academy of Fishery Sciences

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    为了研究含硒谷胱甘肽过氧化物酶(selenium-dependent glutathione peroxidase,Se-GPx)在斑节对虾应激反应和卵巢发育中的作用,实验以斑节对虾肝胰腺转录组数据中筛选获得的Se-GPx基因(Pm Se-GPx)片段为基础,利用RACE技术获得Pm Se-GPx基因的cDNA全长,并对其进行了生物信息学分析;利用荧光定量PCR技术研究了Pm Se-GPx在斑节对虾不同组织、卵巢发育各期、肝胰腺组织在pH9、硫酸铜(Cu2+)应激下的相对表达量和变化趋势。结果显示,Pm Se-GPx基因cDNA全长为959 bp,5’非编码区(UTR)长10 bp,开放阅读框(ORF)长639 bp,编码212个氨基酸,310 bp的3’UTR包含一个硒代半胱氨酸插入序列(SECIS),ORF中的密码子209TGA211编码硒代半胱氨酸(selenocysteine,U67)。实时定量PCR实验结果表明,Pm Se-GPx在斑节对虾的肝胰腺、卵巢、精巢、心脏等组织中均有表达,其中肝胰腺中表达量显著高于其他组织,卵巢次之;卵巢发育阶段表达结果则显示Pm Se-GPx在卵巢发育各期均有表达,在卵巢Ⅲ期表达量最高,其次是V期;在Cu2+胁迫下,其表达量总体呈现先下降后上升然后又下降的趋势;在环境pH为9胁迫下,表达趋势呈现先下降,后回升,然后又下降,再大幅上升的趋势。研究表明,Se-GPx在斑节对虾卵巢发育过程中具有重要作用,且Se-GPx参与斑节对虾对环境理化因子应激的免疫调控。

    Abstract:

    Selenium-dependent glutathione peroxidase(denoted as Se-GPx)plays an important role in the enzymatic antioxidant defense system. It clears the reactive oxygen species (ROS) to avoid the cellular damage. In order to study the function of Se-GPx in immune system and the ovarian development of Penaeus monodon, the full-length cDNA sequence of Se-GPx from black tiger shrimps (denoted as Pm Se-GPx) was obtained by high-throughput transcriptome sequencing and RACE. The full-length cDNA of Pm Se-GPx is 959 bp, including an open reading frame (ORF) of 639 bp encoding a polypeptide of 212 amino acids, a 5'UTR of 10 bp and a 3'UTR of 310 bp containing a conserved selenocysteine insertion sequence (SECIS) element. The molecular mass of the deduced amino acid (aa) sequence was 23.65 kDa with an estimated pI of 4.61. Blast and phylogenetic analyses suggest that Pm Se-GPx is a new member of the shrimp GPxs family. The tertiary structure of Pm Se-GPx protein presents like a bag and there is a catalysis site, which contains couplet of four conservative residues (cysteine C/selenocysteine U, glutamine Q, tryptophan W and asparagine N). Pm Se-GPx mRNA expression was detected in nine tissues by real-time PCR. Pm Se-GPx mRNA expressed was the highest in the hepatopancreas and moderate in the ovary. The result showed that Pm Se-GPx was expression mainly in hepatopancreas which plays an important role in detoxification. At different stages of ovary development, Pm Se-GPx was expressed highly at StageⅢ and Stage V, which indicated a large number of ROS may be produced during these development stages. Pm Se-GPx may protect the ovary from the oxidization damage. Under the stress of Cu2+, the expression of Pm Se-GPx showed a trend of decline, but recovered at 48 h, and then decreased. The result showed that the stress of Cu2+ may inhibit the expression of Pm Se-GPx. Under the stress of pH 9, expression trend of Pm Se-GPx first declined, but recovered at 24 h, then rose significantly at the 96 h. The result showed that neutral environment may inhibit the expression of Pm Se-GPx but aqueous alkaline medium may promote it. Presumably, Se-GPx plays an important role during the ovarian development and immune regulation of P. monodon. Our study provides a basis for further research in reproduction and immunology of P. monodon.

    参考文献
    相似文献
    引证文献
引用本文

唐蕾,傅明骏,赵超,邱丽华,刘文生,江世贵.斑节对虾含硒谷胱甘肽过氧化物酶基因全长克隆及表达分析[J].水产学报,2016,40(11):1664~1673

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2015-08-24
  • 最后修改日期:2016-07-05
  • 录用日期:2016-11-15
  • 在线发布日期: 2016-11-25
  • 出版日期: