陆爱金1,
杜士林1,
陈双凤1,
陈旺光1,
梁延鹏1,2,3,
黄亮亮1,2,3,
曾鸿鹄1,2,3,,
1. 桂林理工大学环境科学与工程学院, 桂林 541004;
2. 广西环境污染控制理论与技术重点实验室, 桂林 541004;
3. 岩溶地区水污染控制与用水安全保障协同创新中心, 桂林 541004
作者简介: 宋晓红(1990-),女,硕士,实验师,研究方向为水生毒理学,E-mail:sxh215@163.com.
通讯作者: 曾鸿鹄,zenghonghu@glut.edu.cn
基金项目: 国家自然科学基金资助项目(51578171);广西科技计划项目(桂科AD18126018);广西自然科学基金资助项目(2018GXNSFAA281022)中图分类号: X171.5
Cloning of P-Glycoprotein Gene and Effects of Triclosan on Its mRNA Expression in Mosquitofish (Gambusia affinis)
Song Xiaohong1,2,3,Lu Aijin1,
Du Shilin1,
Chen Shuangfeng1,
Chen Wangguang1,
Liang Yanpeng1,2,3,
Huang Liangliang1,2,3,
Zeng Honghu1,2,3,,
1. College of Environmental Science and Engineering, Guilin University of Technology, Guilin 541004, China;
2. Guangxi Key Laboratory of Environmental Pollution Control Theory and Technology, Guilin 541004, China;
3. Collaborative Innovation Center for Water Pollution Control and Water Safety in Karst Area, Guilin 541004, China
Corresponding author: Zeng Honghu,zenghonghu@glut.edu.cn
CLC number: X171.5
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摘要:三氯生(TCS)是一种广谱高效抗菌剂,在水环境和生物体内均不同程度检出,对水生生物具有潜在风险。P-糖蛋白(P-gp)是生物体多型异源物质抗性防御系统中重要的"膜解毒蛋白",对水生生物体内的有毒物质和代谢产物具有重要的外排和转运作用。为探究P-gp在鱼类免疫中的作用,克隆了食蚊鱼(Gambusia affinis)P-gp基因的cDNA,检测了不同浓度(50、100和150 □g·L-1) TCS暴露12 h、1 d、3 d、5 d、7 d和9 d后,P-gpmRNA相对表达量的变化。实验获得的食蚊鱼P-gpcDNA共5 452 bp,编码1 294个氨基酸,具有ABC转运蛋白家族典型的跨膜结构、功能区域和作用位点,与其他鳉形目的鱼类P-gp氨基酸序列同源性较高。TCS对P-gpmRNA表达的影响呈现倒"U"型的时间-剂量效应,50 □g·L-1和100 □g·L-1 TCS胁迫后P-gp表达量先升高后下降,100 □g·L-1暴露组表达高峰在暴露1 d时,50 □g·L-1 TCS暴露组表达高峰延迟至3 d,而150 □g·L-1暴露组P-gp表达无显著变化。结果表明,P-gp基因参与了TCS胁迫的解毒过程,有助于食蚊鱼抵抗外源污染物的毒性作用。
关键词: 三氯生/
食蚊鱼/
P-糖蛋白基因/
cDNA克隆/
mRNA表达
Abstract:Triclosan (TCS) is a broad-spectrum antibacterial agent that has been detected in different environmental media and organisms at concentrations ranging from ng·L-1 to □g·L-1, which indicates the high ecological risk to aquatic organisms. P-glycoprotein (P-gp) is an important "membrane detoxification protein" in multixenobiotic resistance system, and plays an important role on the efflux and transport of toxic substances and metabolites in aquatic organisms. To investigate how P-gp functions in fish immunization, the cDNA of P-gp in Gambusia affinis was cloned, and the relative mRNA expression of P-gp was also tested after TCS exposure at different concentrations (50, 100 and 150 □g·L-1) for 12 h, 1 d, 3 d, 5 d, 7 d and 9 d. The newly identified P-gp gene of G. affinis was 5 452 bp in length with an open reading frame (ORF) of 3 885 bp encoding a polypeptide of 1 294 amino acids, it contained the typical transmembrane domains, conserved motifs and functional sites of the ABC transporter family and showed high identities with the P-gp amino acid sequences of other fishes in Cyprinodontiformes. P-gp mRNA expression increased firstly and then decreased, showing a time-dose effect pattern with inverted "U"-type changes in the 50 □g·L-1 and 100 □g·L-1 TCS group. The highest expression of P-gp in 100 □g·L-1 TCS group occured after 1 d exposure, while the expression peak in the 50 □g·L-1 group was delayed to 3 d, and the P-gp expression in the 150 □g·L-1 group had no significant change. Taken together, the P-gp was involved in the detoxification process of TCS exposure and contributed to the resistance of G. affinis against pollutants.
Key words:triclosan/
Gambusia affinis/
P-glycoprotein gene/
cDNA cloning/
mRNA expression.
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