Liao Wan-Qin, Liang Xu-Fang, Wang Lin, Lei La-Mei, Han Bo-Ping
College of Life Science and Technology, Jinan University, Shipai, Guangzhou 510632, People's Republic of China.
J Biochem Mol Toxicol. 2006;20(3):114-26. doi: 10.1002/jbt.20125.
Two full-length cDNAs encoding glutathione S-transferase (GST) were cloned and sequenced from the hepatopancreas of planktivorous silver carp (Hypophthalmichthys molitrix) and bighead carp (Aristichthys nobilis). The silver carp and bighead carp GST cDNA were 920 and 978 bp in length, respectively, and both contained an open reading frame that encoding 223 amino acids. Partial GST cDNA sequences were also obtained from the liver of grass carp (Ctenopharyngodon idellus), crucian carp (Carassius auratu), mud carp (Cirrhinus molitorella), and tilapia (Oreochromis nilotica). All these GSTs could be classified as alpha-class GSTs on the basis of their amino acid sequence identity with other species. The three-dimensional structure of the silver carp GST was predicted using a computer program, and was found to fit the classical two-domain GST structure. Using the genome walker method, a 875-bp 5'-flanking region of the silver carp GST gene was obtained, and several lipopolysaccharide (LPS) response elements were identified in the promoter region of the phytoplanktivorous fish GST gene, indicating that the GST gene expression of this fish might be regulated by LPS, released from the toxic blue-green algae producing microcystins. To compare the constitutive expression level of the liver GST gene among the six freshwater fishes with completely different tolerance to microcystins, beta-actin was used as control and the ratio GST/beta-actin mRNA (%) was determined as 130.7 +/- 6.6 (grass carp), 103.1 +/- 8.9 (bighead carp), 92.6 +/- 15.0 (crucian carp), 72.3 +/- 7.8 (mud carp), 58.8 +/- 11.5 (silver carp), and 33.6 +/- 13.7 (tilapia). The constitutive expression level of the liver GST gene clearly shows that all the six freshwater fishes had a negative relationship with their tolerance to microcystins: high-resistant fishes (phytoplanktivorous silver carp and tilapia) had the lowest tolerance to microcystins and the high-sensitive fish (herbivorous grass carp) had the highest tolerance to microcystins. Taken together with the reciprocal relationship of constitutive and inducible liver GST expression level in some of the tested fish species to microcystin exposure, a molecular mechanism for different microcystin detoxification abilities of the warm freshwater fishes was discussed.
从食浮游生物的鲢鱼(Hypophthalmichthys molitrix)和鳙鱼(Aristichthys nobilis)的肝胰腺中克隆并测序了两个编码谷胱甘肽S-转移酶(GST)的全长cDNA。鲢鱼和鳙鱼的GST cDNA长度分别为920和978 bp,两者均包含一个编码223个氨基酸的开放阅读框。还从草鱼(Ctenopharyngodon idellus)、鲫鱼(Carassius auratu)、鲮鱼(Cirrhinus molitorella)和罗非鱼(Oreochromis nilotica)的肝脏中获得了部分GST cDNA序列。根据它们与其他物种的氨基酸序列同一性,所有这些GST都可归类为α-类GST。使用计算机程序预测了鲢鱼GST的三维结构,发现其符合经典的双结构域GST结构。采用基因组步移法获得了鲢鱼GST基因875 bp的5'-侧翼区,并在食浮游生物鱼类GST基因的启动子区域鉴定出几个脂多糖(LPS)反应元件,表明该鱼类的GST基因表达可能受产微囊藻毒素的有毒蓝藻释放的LPS调控。为比较六种对微囊藻毒素耐受性完全不同的淡水鱼肝脏GST基因的组成性表达水平,以β-肌动蛋白为对照,测定GST/β-肌动蛋白mRNA的比率(%)为130.7±6.6(草鱼)、103.1±8.9(鳙鱼)、92.6±15.0(鲫鱼)、72.3±7.8(鲮鱼)、58.8±11.5(鲢鱼)和33.6±13.7(罗非鱼)。肝脏GST基因的组成性表达水平清楚地表明,所有这六种淡水鱼与其对微囊藻毒素的耐受性呈负相关:高抗性鱼类(食浮游生物的鲢鱼和罗非鱼)对微囊藻毒素的耐受性最低,而高敏感性鱼类(草食性草鱼)对微囊藻毒素的耐受性最高。结合一些受试鱼类肝脏GST组成性和诱导性表达水平与微囊藻毒素暴露的相互关系,讨论了暖水性淡水鱼不同微囊藻毒素解毒能力的分子机制。