海洋生物学

黄斑篮子鱼去毒相关基因的克隆与肝脏组成型表达分析

  • 王琳 ,
  • 梁旭方 ,
  • 林群 ,
  • 李光照 ,
  • 胡永乐
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  • 暨南大学生命科学技术学院, 广东 广州 510632
王琳(1980— ),女,山西省人,博士,主要从事鱼类去毒相关基因研究工作。

收稿日期: 2007-11-28

  修回日期: 2008-04-09

  网络出版日期: 2009-12-12

基金资助

国家科技部“863”项目(2007AA09Z437), 国家自然科学基金项目(30670367), 广东省科技计划项目(2007B020701002;2005B20301005), 广东省自然科学基金项目(031886)和教育部留学回国人员科研启动基金项目

Molecular cloning of cDNA core sequences of detoxification-related genes and liver constitutive expression in rabbitfish Siganus oramin

  • WANG Lin ,
  • LIANG Xu-fang ,
  • LIN Qun ,
  • Li Guang-zhao ,
  • Hu Yong-le
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  • College of Life Science and Technology, Jinan University, Guangzhou 510632, China
王琳(1980— ),女,山西省人,博士,主要从事鱼类去毒相关基因研究工作。

Received date: 2007-11-28

  Revised date: 2008-04-09

  Online published: 2009-12-12

Supported by

国家科技部“863”项目(2007AA09Z437), 国家自然科学基金项目(30670367), 广东省科技计划项目(2007B020701002;2005B20301005), 广东省自然科学基金项目(031886)和教育部留学回国人员科研启动基金项目

摘要

从基因水平探讨海洋鱼类对海洋藻毒素的去毒分子机理。采用RT-PCR法成功克隆了黄斑篮子鱼Siganus oramin肝脏I时相代谢酶细胞色素P450 1A(CYP1A)、II时相代谢酶alpha型谷胱甘肽S-转移酶(GSTA)和rho型谷胱甘肽S-转移酶(GSTR)、热休克蛋白70 (HSP70)、alpha 1型钠钾ATP酶(ATP1A1)及β-肌动蛋白(beta-actin, ACT)基因cDNA核心序列,序列分别长879 bp、582 bp、588 bp、660 bp、749 bp和554 bp。序列同源性分析发现,属鲈形目的黄斑篮子鱼CYP1A、GSTA和GSTR与同属鲈形目的牙鲆Paralichthys olivaceus、欧洲鲽Pleuronectes platessa、真鲷Pagrus major、鲤形目的斑马鱼Brachydanio rerio 相应氨基酸序列同源性较高,CYP1A和GSTA与非洲爪蟾(两栖类)、鸡(鸟类)、小鼠、大鼠和人(哺乳类)相应氨基酸序列同源性低,这可能与鱼类I、II时相去毒酶基因承担水环境毒素去毒代谢的特殊功能有关;而HSP70、ATP1A和β-肌动蛋白在鱼类、两栖类、鸟类、哺乳类中均有较高的同源性,这可能与这些基因在机体中承担的最基本的生命功能相关。应用半定量RT-PCR的方法,以β-肌动蛋白作为外参照,在指数期增长范围内分别得到了CYP1A、GSTA、GSTR、HSP70和ATP1A1 mRNA与β-肌动蛋白mRNA (%)的比值,确定黄斑篮子鱼肝脏去毒相关基因的组成型表达水平。其中,黄斑篮子鱼肝脏CYP1A、GSTA和GSTR基因组成型表达相对较高,HSP70和ATP1A1基因组成型表达相对较低,这可能与不同基因在黄斑篮子鱼海洋藻毒素去毒分子机理中承担的作用相关,为海洋藻毒素在海洋鱼类中的积聚及代谢去毒分子机制的研究提供了相关数据。

本文引用格式

王琳 , 梁旭方 , 林群 , 李光照 , 胡永乐 . 黄斑篮子鱼去毒相关基因的克隆与肝脏组成型表达分析[J]. 热带海洋学报, 2009 , 28(6) : 79 -87 . DOI: 10.11978/j.issn.1009-5470.2009.06.079

Abstract

Partial cDNA sequences of hepatic cytochrome P-450 1A (CYP1A), glutathione S-transferase alpha (GSTA), glutathione S-transferase rho (GSTR), heat shock protein 70 (HSP70), Na+/K+-ATPase alpha 1(ATP1A1) and beta-actin (ACT) genes from rabbitfish (Siganus oramin) were obtained by PCR using degenerate primers. These sequences were 879 bp, 582 bp, 588 bp, 660 bp, 749 bp and 554 bp in length, respectively. Homology of the CYP1A, GSTA and GSTR amino acid sequence are high with bastard halibut (Paralichthys olivaceus), European plaice (Pleuronectes platessa), red sea bream (Pagrus major) and zebrafish CYP1A, GSTA and GSTR, and CYP1A and GSTA are low with human, rat, mouse, chicken and African clawed frog. The identities of HSP70, ATP1A and beta-actin amino acid sequences are highly conserved between fish, bird, amphibian and mammals. Using semi-quantitative PCR within the exponential phase, with beta-actin as an external control, the constitutive transcriptional expression of genes of phase I (CYP1A), phase II (GSTA and GSTR) xenobiotic metabolizing enzymes (XMEs), HSP70 and ATP1A1 were also investigated. The levels of CYP1A, GSTA and GSTR mRNA expression were higher, and the levels of HSP70 and ATP1A1 mRNA expression were lower. The constitutive expression pattern of these genes, show an accordant relationship with their functions, which provide data for our understanding to the detoxification mechanism of marine algae toxin in marine fish.

参考文献

[1] White A W. Can. J. Fish. Aquat Sci, 1980, 37: 2262-2265.
[2] White A W. Paralytic shellfish toxins and finfish [A], In: Ragelis, E P (ed.) Seafood toxins [M]. ACS sympodium series 262. Amer Chem Soc, Washington D C, 1984, 171-180.
[3] Bricelj V M, LEE J H, CEMBELLA A D. Influence of dinoflagellate cell toxicity on uptake and loss of paralytic shellfish toxins in the northern quahog, Mercenaria mercenaria[J]. Mar Ecol Prog Ser, 1990, 74: 33-46.
[4] BRICELJ V M, LEE J H, ANDERSON D M. Uptake kinetics of paralytic shellfish toxins from the dinoflagellate Alexandrium fundyense in the mussel Mytilus edulis[J]. Mar Ecol Progr Ser, 1991, 63: 177-188.
[5] CHEN, C Y, CHOU, H N. Fate of paralytic shellfish poisoning toxins in purple clam Hiatula rostrata, in outdoor culture and laboratory culture[J]. Marine pollution Bulletin, 2002, 44: 733-738.
[6] SHUMWAY S E. Toxic algae, a threat to shellfish farming. World Aquacult, 1989, 20(3): 65-74.
[7] BEATTIE K A, RESSLER J, WIEGAND C, et al. Comparative effects and metabolism of two microcystins and nodularin in the brine shrimp Artemia salina [J]. Aquat Toxicol, 2003, 62: 219-226.
[8] GUBBINS M J, EDDY F B, GALLACHER S, STAGG R M. Paralytic shellfish poisoning toxins induce xenobiotic metabolizing enzymes in Atlantic salmon (Salmo salar)[J]. Marine Environmental Research, 2000, 50: 479-483.
[9] STAGG RM, GALLACHER S, BURGESS P. Harmful algae. In Reguera J B, Blanco M L, FernaÂndez & T Wyatt, Xunta de Galicia and Intergovernmental Oceanographic Commission of UNESCO[R]. UNESCO, Santiago de Compostela, 1998:607-608.?
[10]LIAO W Q, LIANG X F, WANG L, et al. Molecular cloning and characterization of alpha-class glutathione S-transferase gene from the liver of silver carp, bighead carp and other major Chinese freshwater fishes [J]. J Biochem Mol Toxicol, 2006, 20: 114-126.
[11]LIAO W Q, LIANG X F, WANG L, et al. Structural conservation and food habit-related liver expression of uncoupling protein 2 gene in five major Chinese freshwater fishes [J]. J Biochem Mol Biol, 2006, 39(4): 346-354.
[12]WANG L, LIANG X F, LIAO W Q, et al. Structural and functional characterization of microcystin detoxification-related liver genes in a phytoplanktivorous fish, Nile tilapia (Oreochromis niloticus) [J]. Comp Biochem Physiol C, 2006, 144: 216-227.
[13] FENG Q, BOONE A N, VIJAYAN M M. Copper impact on heat shock 70 expression and apoptosis in rainbow trout hepatocytes[J]. Comp Biochem Physiol C Toxicol Pharmacol, 2003, 135: 345-355.
[14] PAVLOV K V, SOKOLOV V S. Electrogenic Ion Transport by Na+/K+ -ATPase[J]. Membr Cell Biol, 2000, 13: 745-788.
[15] TANG J Y M, WONG C K C, AU D W T. The ichthyotoxic alga chattonella marina induces Na+, K+ -ATPase, and CFTR proteins expression in fish gill chloride cells in vivo[J]. Biochemical and Biophysical Research Communications, 2007, 353: 98-103.

 

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