›› 2012, Vol. 55 ›› Issue (5): 520-526.doi:

• 研究论文 • 上一篇    下一篇

飞蝗谷胱甘肽S-转移酶基因克隆、 序列分析及表达特征

张学尧, 王建新, 郭艳琼, 张建珍, 马恩波   

  1. 山西大学应用生物学研究所, 太原 030006
  • 收稿日期:2012-01-06 修回日期:2012-03-28 出版日期:2012-05-20 发布日期:2012-05-20
  • 通讯作者: 张建珍, 马恩波 E-mail:maenbo2003@sxu.edu.cn; zjz@sxu.edu.cn
  • 作者简介:张学尧, 男, 1981年11月生, 山西临汾人, 博士, 讲师, 研究方向为昆虫生物化学与分子生物学, E-mail: zxy@sxu.edu.cn; 王建新, 男, 1987年5月生, 硕士, 研究方向昆虫生物化学与分子生物学, E-mail: wang_jian_xin@163.com
  • 基金资助:

     国家自然科学基金项目(30970410, 31101463); 国家自然基金重大国际合作项目(30810103907); 高等学校博士学科点专项科研基金(20111401110006, 20111401120009); 农业部公益性行业科研专项(200903021)

Cloning, sequence analysis and expression profiling of glutathione Stransferase omega 1 gene from Locusta migratoria (Orthoptera: Acridoidea)

ZHANG Xue-Yao, WANG Jian-Xin, GUO Yan-Qiong, ZHANG Jian-Zhen, MA En-Bo   

  • Received:2012-01-06 Revised:2012-03-28 Online:2012-05-20 Published:2012-05-20
  • Contact: ZHANG Jian-Zhen, MA En-Bo E-mail:maenbo2003@sxu.edu.cn; zjz@sxu.edu.cn
  • About author:zxy@sxu.edu.cn; wang_jian_xin@163.com

摘要: 谷胱甘肽S-转移酶(glutathione S-transferase, GST)是一类广泛分布的多功能超家族酶系, 其中Omega家族GST在昆虫体内担负重要生理功能。为探讨飞蝗Locusta migratoria Omega家族GST功能, 利用RT-PCR技术克隆得到1条飞蝗谷胱甘肽S-转移酶Omega家族基因全长cDNA, 命名为LmGSTo1 (GenBank登录号: JQ750592)。该基因开放阅读框长738 bp, 编码245个氨基酸。该酶含有N-端和C-端2个结构域, N-端结构域由5个β-折叠和3个α螺旋组成, 包括4个GSH结合位点; C-端结构域由8个α螺旋组成, 含有5个底物结合位点。Real-time PCR结果表明, LmGSTo1在飞蝗不同龄期均有表达, 在胃盲囊和中肠表达量较低, 在前肠、马氏管、肌肉和脂肪体表达量较高; 溴氰菊酯处理可导致LmGSTo1表达水平显著下降。这些结果为进一步研究LmGSTo1基因功能提供了依据。

关键词: 飞蝗, 谷胱甘肽S-转移酶, 基因克隆, 序列分析

Abstract: Glutathione S-transferases are a ubiquitous superfamily of multifunctional enzymes, in which Omega-class GST is responsible for important physiological function in insects. In this study, the full-length cDNA of a GST Omega gene from Locusta migratoria was cloned by RT-PCR technique, and named as LmGSTo1 (GenBank accession no. JQ750592). The open reading frame (ORF) of LmGSTo1 is 738 bp in length coding 245 amino acids. LmGSTO1 consists of an N-terminal domain and a C-terminal domain. The N-terminal domain includes five β-sheets and three α-turns, while the C-terminal domain is composed of eight α-turns. Temporal expression pattern revealed that LmGSTo1 was constitutively expressed in all developmental stages of the locust. Tissue expression profiling further indicated that LmGSTo1 was slightly expressed in midgut and gastric caecum and had higher expression levels in foregut, Malpighian tubules, fat body and muscle. The expression level of LmGSTo1 was significantly decreased after deltamethrin treatment. The results provide a basis for further studying the function of LmGSTo1.

Key words: Locusta migratoria, glutathione S-transferase (GST), gene cloning, sequence analysis