中国寄生虫学与寄生虫病杂志 ›› 1998, Vol. 16 ›› Issue (4): 256-259.

• 论著 • 上一篇    下一篇

编码肝片吸虫GST和猪蛔虫GST基因的测序及同源性分析

孙文宇; 刘述先   

  1. 中国预防医学科学院寄生虫病研究所
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:1998-08-28 发布日期:1998-08-28

SEQUENCING AND HOMOLOGY ANALYSIS OF cDNAS ENCODING FhGST AND AsGST *

Sun Wenyu; Liu Shuxian   

  1. Institute of Parasitic Diseases **; Chinese Academy of Preventive Medicine; Shanghai 200025
  • Received:1900-01-01 Revised:1900-01-01 Online:1998-08-28 Published:1998-08-28

摘要: 目的:比较肝片吸虫GST(FhGST)、猪蛔虫GST(AsGST)基因与日本血吸虫26GST(Sj26GST)间的同源性。方法:以盐酸胍/氯化铯梯度超速离心法提取肝片吸虫和猪蛔虫的总RNA,合成两对特异性引物,通过反转录-PCR将所需的编码GST的cDNA扩增出来,并将PCR产物直接测序。应用DNASIS软件比较FhGST、AsGST基因与Sj26GST间的同源性。结果:测序得到FhGST403bp片段和AsGST411bp片段。结论:FhGST和AsGST片段与
Sj26GST的cD-NA在核苷酸水平上的同源性分别为59%和54%,两片段间的同源性为52%。

关键词: FhGST, AsGST, 反转录-PCR, 同源性

Abstract:

AIM: To study the homologies between FhGST, AsGST and Sj26GST. METHODS: Total RNAs
were extracted from Fasciola hepatica(Fh) and Ascaris suum(As) by guanidine hydrochloride/CsCl
ultra centrifugation. Two pairs of primers were designed according to FhGST and AsGST sequences.
RT PCR was carried out using total RNA as template. PCR products were directly sequenced. Then
the homology analysis was made using DNASIS software on nucleotide level. RESULTS: A FhGST403 bp
fragment and a AsGST411 bp fragment were obtained and they both located in the open reading frame. CONCLUSION: On nucleotide level, the homologies are 59% and 54% between the two cloned fragments and Schistosoma japonicum 26 kDa GST (Sj26GST) respectively

Key words: FhGST, AsGST, RT PCR, homology