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鱼类谷胱甘肽转移酶基因cDNA克隆及其序列分析 被引量:3

Cloning and the sequence analysis of the fish glutathione transferase Pi gene
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摘要 采用RT-PCR方法,从鲢、鲤、鲫3种鱼类肝脏总RNA中克隆出了谷胱甘肽转移酶Pi型(GST Pi)cDNA序列,推导了其编码的氨基酸序列。3种鱼类GST Pi的ORF全长627bp,编码208个氨基酸。翻译起始密码均为ATG,终止密码子均为TGA。鱼类与哺乳动物、两栖类爪蟾以及节肢动物丝虫之间GST Pi氨基酸序列相似度平均值分别为50%、33%、15%左右。5种鱼类之间的氨基酸序列相似度较大,其中鲤科鱼类之间平均为85%左右。我们以GST Pi为分子标记,用最大简约数法(MP)构建了13个物种的系统进化树,识别出两个大的单系类群:哺乳类组成类群一(bootstrap100);鱼类组成类群二(bootstrap93)。通过比较鱼类与哺乳类GST Pi N末端和C末端功能域的氨基酸组成差异,探讨了淡水鱼类GSTs承担较强的微囊藻毒素去毒能力的可能分子机制。 Using RT-PCR method, the glutathione transferase Pi cDNAs were cloned from Cyprinus carpio, Hypophthalmichthys molitrix, and Carassius auratus. The open reading frames (ORFs) from the 3 fishes were 627 bp long (encoding for 208 amino acids) with the initial code ATG and the terminal code TGA. The sequence similarity was 50% between fish and mammals, 33% between fish and amphibian, and 15% between fish and arthropoda, respectively. The sequence similarity was big among fishes, and the average value of the 4 cyprinids was about 85%. Phylogenetic tree was constructed for 13 species based on GST Pi amino acid sequences using MP (Maximum Parsimony) method. Two major clusters were recognized: cluster one consisted of Mammals (bootstrap 100) and cluster two consisted of fishes (bootstrap 93). Based on the sequences analyses of N/C domain of GST Pi, we proposed the detoxification mechanism of freshwater fishes that were thought to have stronger tolerance to microcystins.
出处 《遗传》 CAS CSCD 北大核心 2007年第3期349-354,共6页 Hereditas(Beijing)
基金 国家自然科学基金(编号:30530170) 华中农业大学科研启动基金(编号:52204-04031) 华中农业大学大学生科技创新基金资助~~
关键词 谷胱甘肽转移酶Pi型 glutathione transferase Pi Cyprinus carpio Hypophthalmichthys molitrix Carassius auratus
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参考文献14

  • 1Sheehan D,Meade G,Foley VM,Dowd A.Structure,function and evolution of glutathione transferases:implications for classification of non-mammalian members of an ancient enzyme superfamily,Biochem J,2001,360:1-16.
  • 2Hayes JD,Flanagan JU,Jowsey IR.Glutathione transferases.Annu Rev Pharmacol Toxicol,2005,45:51-88.
  • 3Konishi T,Kato K,Araki T,Shiraki K,Takagi M,Tamaru Y.A new class of glutathione S-transferase from the hepatopancreas of the red sea bream Pagrus major.Biochem J,2005,388:299-307.
  • 4Cowell IG,Dixon KH,Pemble SE,Ketterer BK,Taylor JB.The structure of the human glutathione S-transferase 7r gene.Biochem J,1988,255:79-83.
  • 5George SG.Enzymology and molecular biology of phase Ⅱ xenobiotic-conjugating enzymes in fish.In:Malins,DC,Ostrander GK eds,Aquatic Toxicology:Molecular,Biochemical,and Cellular Perpectives.Lewis Publishers,CRC Press,1994,37-85.
  • 6Riol M,Valinas N,Fernandez G,Lopez P.Glutathione S-transferases from rainbow trout liver and freshly isolated hepatocytes:purification and characterization.Comp Biochem Physiol C Toxicol Pharmacol,2001,128:227-235.
  • 7廖婉琴,梁旭方,王琳,方玲,雷腊梅,韩博平.淡水鱼类微囊藻毒素去毒酶基因的克隆[J].生态科学,2005,24(1):6-8. 被引量:10
  • 8López P,Vali(n)as N,Riol M.Glutathione S-transferase cytosolic isoforms as biomarkers of polychlorinated biphenyl (Arochlor-1254) experimental contamination in rainbow trout.Toxicol Lett,2002,136:97-106.
  • 9刘新仿,李家洋.紫外线强烈诱导的谷胱甘肽转移酶基因的功能鉴定[J].Acta Genetica Sinica,2002,29(5):458-460. 被引量:16
  • 10Chen J,Xie P.Tissue distributions and seasonal dynamics of the hepatotoxic microcystins-LR and -RR in two freshwater shrimps,Palaemon modestus and Macrobrachium nipponensis,from a large shallow,eutrophic lake of the subtropical China.Toxicon,2005,45:615-625.

二级参考文献9

  • 1汤钊猷.原发性肝癌[M].上海:上海科学技术出版社,1989.30-37.
  • 2Chorus I, Falconer I R, Salas H J, et al., 2000. Health risks caused by freshwater cyanobacteria in recreational waters[J].J. Toxicol. Environ. Health 3, 323-347.
  • 3Krienitz L, Ballot A, Kotut K, et al. 2003. Contribution of hot spring cyanobacteria to the misterious deaths of lesser Flamingos at Lake Bogoria, Kenya[J]. FEMS Microbiol. Ecol.43, 141-148.
  • 4Sivonen K, Niemela S I, Lepisto L, et al. 1990. Toxic cyanobacterial (blue-green algae) in finish fresh and canstal waters[J] Hydrobiologia, 190: 267- 2751.
  • 5Hitzfeld B C, Hoger S J, Dietrich R. 2000. Cyanobacterial toxins: removal during drinking water treatment, and human risk assessment[J]. Environ. Health Perspect. 10, 113-122.
  • 6Pfugmacher S, Wiegand C, Oberemm A, et al. 1998.Identification of an enzymatically formed glutathione conjugate of the cyanobacterial hepatotoxin microcystin-LR: the first step of detoxication[J]. Biochim. et Biophys. Acta 1425: 527-533.
  • 7Wiegand C, Pfugmacher S, Giese M H. et al. 2000. Uptake,Toxicity, and Effects on Detoxication Enzymes of Atrazine and Trifluoroacetate in Embryos of Zebrafish[J]. Ecotoxicol.and Environm. Safety 45:122-131.
  • 8Best J H, Eddy F B, Codd G A. 2003. Effects of Microcystis cells, cell extracts and lipopolysaccharide on drinking and liver function in rainbow trout Oncorhynchus mykiss Walbaum. Aquat[J]. Toxicol. 64: 419-426.
  • 9Yuxin Hu,Chang Han,Zhonglin Mou,Jiayang Li.Monitoring gene expression by cDNA array[J].Chinese Science Bulletin,1999,44(5):441-444. 被引量:3

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