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泥蚶谷胱甘肽过氧化物酶基因的全长克隆与表达分析
引用本文:程雪艳,蒋国萍,柴雪良,滕爽爽.泥蚶谷胱甘肽过氧化物酶基因的全长克隆与表达分析[J].水生生物学报,2016,40(6):1144-1151.
作者姓名:程雪艳  蒋国萍  柴雪良  滕爽爽
作者单位:1. 浙江省海洋水产养殖研究所,温州 325005; 温州医科大学检验医学院,生命科学学院,温州 325035; 浙江省近岸水域生物资源开发和保护重点实验室,温州 325005;2. 浙江省海洋水产养殖研究所,温州 325005; 浙江省近岸水域生物资源开发和保护重点实验室,温州 325005; 上海海洋大学水产与生命学院,上海 201306;3. 浙江省海洋水产养殖研究所,温州 325005; 温州医科大学检验医学院,生命科学学院,温州 325035; 浙江省近岸水域生物资源开发和保护重点实验室,温州 325005; 上海海洋大学水产与生命学院,上海 201306;4. 浙江省海洋水产养殖研究所,温州 325005; 浙江省近岸水域生物资源开发和保护重点实验室,温州 325005
基金项目:国家高技术研究发展计划(2012AA10A410-1),浙江省重大科技专项(2012C12907-4),温州市种子种苗科技创新专项(N20120017)资助[Supported by National High Technology Research and Development Program of China (863 Program)(2012AA10A410-1),Major Science and Technology Projects of Zhejiang Province(2012C12907-4),Seed Science and Technology Innovation Project of Wenzhou City(N20120017)
摘    要:为了探讨谷胱甘肽过氧化物酶(Glutathione peroxidase,GPx)基因在泥蚶应激反应中的作用,研究采用RACE技术克隆了泥蚶GPx基因(TgGPx)cDNA全长,其cDNA全长1195 bp,包含45 bp 5’-UTR,639 bp开放阅读框(ORF)和511 bp 3’-UTR。ORF编码212个氨基酸残基,预测蛋白分子量为24.3 kD,理论等电点为8.33,其中,第53个氨基酸U是由密码子202UGA204编码的硒代半胱氨酸(Se-Cys)。在3’-UTR上存在一段序列,形成一种独特的茎环结构,即SECIS元件。SECIS元件在密码子UGA翻译为Se-Cys的过程中起决定性作用。通过序列比对与系统进化分析,发现软体动物中也存在不同种类的GPx基因,TgGPx与GPx1和GPx2的亲缘关系较近。利用qRT-PCR技术对TgGPx在泥蚶的不同组织以及重金属刺激后的表达量进行分析,结果表明,TgGPx在泥蚶的5个组织中都有表达,但存在组织特异性,在外套膜中的表达量最高,在血细胞中的表达量最低。用重金属铅、铜、镉刺激后,TgGPx在肝胰脏中的表达量显著升高,表明TgGPx在维护机体正常功能方面及泥蚶抵御外界刺激的应激反应中发挥作用。

关 键 词:泥蚶    谷胱甘肽过氧化物酶    全长克隆    基因表达
收稿时间:2015-12-23

FULL-LENGTH CDNA CLONING AND EXPRESSION ANALYSIS OF GLUTATHIONE PEROXIDASE FROM BLOOD CLAM TEGILLARCA GRANOSA
Abstract:Glutathione peroxidase (GPx) is an important member of cellular enzymatic antioxidant system regulating stress response of host as an acute protein. In this study, a selenium-dependent glutathione peroxidase (TgGPx) gene from blood clamTegillarca granosa was cloned and analyzed by rapid amplification of cDNA ends (RACE). The nuc-leotide sequence ofTgGPx was consisted of 1195 bp with a 45 bp 5′UTR a of 511 bp 3′UTR and 639 bp open reading frame (ORF) encoding a peptide of 212 amino acids with an estimated molecular mass of 24.3 kD and a theoretical iso-electric point of 8.33.TgGPx had a characteristic codon at202UGA204 that corresponded to Selenocysteine as U53. A sel-enocysteine insertion sequence (SECIS) element was identified in the 3′-UTR ofTgGPx cDNA, which forms a stem-loop secondary structure. SECIS element plays a decisive role in the translation of the stop codon UGA into a seleno-cysteine. Multiple sequence alignment and phylogenetic analysis revealed that there were different types of GPx genes in mollusks.TgGPx has a closer phylogenic relationship with GPx1 and GPx2.TgGPx expressed in all five tissues with the highest mRNA level in mantle and the lowest in haemocytes. The expression pattern ofTgGPx in adult may sup-port its role in adult tissue growth and larval development.TgGPx was significantly up-regulated in hepatopancreas by heavy metals (Zn2+, Cu2+ and Cd2+) exposure, suggestingTgGPx may play a role in stress response and maintaining the body’s normal function inT. granosa.
Keywords:Tegillarca granosa  Glutathione peroxidase  Full length clone  mRNA expression
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