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稀有鮈鲫PKZ基因的分子克隆、特征分析及表达分析

Molecular cloning, characterization and expression analysis of the PKZ gene in rare minnow Gobiocypris rarus.

作者信息

Su Jianguo, Zhu Zuoyan, Wang Yaping

机构信息

State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China.

出版信息

Fish Shellfish Immunol. 2008 Jul;25(1-2):106-13. doi: 10.1016/j.fsi.2008.03.006. Epub 2008 Mar 18.

DOI:10.1016/j.fsi.2008.03.006
PMID:18448359
Abstract

Double-stranded RNA-activated protein kinase (PKR) plays an important role in interferon-induced antiviral responses, and is also involved in intracellular signaling pathways, including the apoptosis, proliferation, and transcription pathways. In the present study, a PKR-like gene was cloned and characterized from rare minnow Gobiocypris rarus. The full length of the rare minnow PKR-like (GrPKZ) cDNA is 1946 bp in length and encodes a polypeptide of 503 amino acids with an estimated molecular mass of 57,355 Da and a predicted isoelectric point of 5.83. Analysis of the deduced amino acid sequence indicated that the mature peptide contains two Zalpha domains and one S_TKc domain, and is most similar to the crucian carp (Carassius auratus) PKR-like amino acid sequence with an identity of 77%. Quantitative RT-PCR analysis showed that GrPKZ mRNA expression is at low levels in gill, heart, intestine, kidney, liver, muscle and spleen tissues in healthy animals and up-regulated by viruses and bacteria. After being infected by grass carp reovirus, GrPKZ expression was up-regulated from 24h post-injection and lasted until the fish became moribund (P<0.05). Following infection with Aeromonas hydrophila, GrPKZ transcripts were induced at 24h post-injection (P<0.05) and returned to control levels at 120 h post-injection. These data imply that GrPKZ is involved in antiviral defense and Toll-like receptor 4 signaling pathway in bacterial infection.

摘要

双链RNA激活蛋白激酶(PKR)在干扰素诱导的抗病毒反应中起重要作用,还参与细胞内信号通路,包括凋亡、增殖和转录通路。在本研究中,从稀有鮈鲫(Gobiocypris rarus)中克隆并鉴定了一个PKR样基因。稀有鮈鲫PKR样(GrPKZ)cDNA全长1946 bp,编码一个由503个氨基酸组成的多肽,估计分子量为57355 Da,预测等电点为5.83。对推导的氨基酸序列分析表明,成熟肽包含两个Zalpha结构域和一个S_TKc结构域,与鲫鱼(Carassius auratus)的PKR样氨基酸序列最相似,同一性为77%。定量RT-PCR分析表明,GrPKZ mRNA在健康动物的鳃、心脏、肠道、肾脏、肝脏、肌肉和脾脏组织中表达水平较低,受病毒和细菌感染后上调。感染草鱼呼肠孤病毒后,GrPKZ表达从注射后24小时开始上调,一直持续到鱼濒死(P<0.05)。感染嗜水气单胞菌后,GrPKZ转录本在注射后24小时被诱导(P<0.05),并在注射后120小时恢复到对照水平。这些数据表明GrPKZ参与抗病毒防御以及细菌感染中的Toll样受体4信号通路。

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