Su Jianguo, Zhu Zuoyan, Wang Yaping
State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China.
Fish Shellfish Immunol. 2008 Jul;25(1-2):106-13. doi: 10.1016/j.fsi.2008.03.006. Epub 2008 Mar 18.
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.
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。