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HEREDITAS ›› 2007, Vol. 29 ›› Issue (3): 349-349―354.doi: 10.1360/yc-007-0349

• 研究报告 • Previous Articles     Next Articles

Cloning and the sequence analysis of the fish glutathione transferase Pi gene

SUN Yu-Hua1, XIE Ping2, GUO Hai-Tao1, XIA Wen-Wei1   

  1. 1. Key Laboratory of Agricultural Animal Genetics, Breeding and Reproduction of Education Ministry, Huazhong Agricultural University, Wuhan 430070, China 2. Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China
  • Received:2006-06-26 Revised:2006-08-30 Online:2007-03-01 Published:2007-03-01
  • Contact: XIE Ping

Abstract:

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 recog-nized: 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.