首页> 外文期刊>Journal of Fish Biology >Identification and expression analysis of the sting gene, a sensor of viral DNA, in common carp Cyprinus carpio
【24h】

Identification and expression analysis of the sting gene, a sensor of viral DNA, in common carp Cyprinus carpio

机译:鲤鱼鲤鱼sting基因(一种病毒DNA传感器)的鉴定和表达分析

获取原文
获取原文并翻译 | 示例
           

摘要

Stimulator of interferon gene (sting) was identified and characterized from common carp Cyprinus carpio. The sting messenger (m) RNA encoded a polypeptide of 402 amino acids with a calculated molecular mass of 46.184 kDa and an isoelectronic point of 6.08. The deduced protein of sting contained a signal peptide, three transmembrane motifs in the N-terminal region and four putative motifs (RXR) found in resident endoplasmic reticulum proteins. mRNA expression of sting was present in twelve investigated tissues, and was up-regulated by koi herpesvirus (KHV) in vivo and in vitro. The transcription of sting was altered by poly(I:C) and poly(dT:dA) stimulation in vitro. The findings suggested that sting is an inducible gene involved in innate immunity against DNA-and RNA-derived pathogens. To investigate defence mechanisms in C. carpio development, sting level in embryos, larvae and juvenile fish was monitored following KHV challenge. The sting message was negligible in embryos prior to hatching, but observed at higher transcriptional levels throughout larval and juvenile stages. Investigation showed the mRNA expression profiles of genes encoding for proteins promoting various functions in the interferon pathway, from pattern recognition receptors to antiviral genes, to be significantly induced in all examined organs by in vivo infection with KHV. Following KHV infection, the ifn message was significantly downregulated in spleen, head kidney, brain and hepatopancreas but notably up-regulated in gill, intestine and skin, suggesting that ifn induction might be related to the mucosal immune system and virus anti-ifn mechanisms. These results provided the basis for further research into the role and mechanisms of sting in fishes. (C) 2016 The Fisheries Society of the British Isles
机译:从鲤鱼鲤鱼中鉴定并鉴定了干扰素基因(sting)的刺激物。刺蛋白(m)RNA编码了402个氨基酸的多肽,计算分子量为46.184 kDa,等电点为6.08。推导的of蛋白包含一个信号肽,在N端区域的三个跨膜基序和在驻留内质网蛋白中发现的四个推定基序(RXR)。 twelve的mRNA表达存在于十二个调查的组织中,并且在体内和体外均被锦鲤疱疹病毒(KHV)上调。在体外,poly(I:C)和poly(dT:dA)刺激改变了ing的转录。这些发现表明,ing是一种可诱导的基因,涉及针对DNA和RNA衍生病原体的先天免疫。为了研究鲤鱼衣原体发育的防御机制,在KHV攻击后监测了胚胎,幼虫和幼鱼中刺痛的水平。在孵化之前,刺痛信息在胚胎中可忽略不计,但在幼虫和幼年阶段以较高的转录水平观察到。研究表明,通过KHV体内感染,在所有检查的器官中都可以显着诱导编码蛋白质的基因的mRNA表达谱,这些蛋白质可以促进干扰素途径中从模式识别受体到抗病毒基因的各种功能。 KHV感染后,ifn信息在脾脏,头部肾脏,大脑和肝胰脏中显着下调,但在ill,肠和皮肤中显着上调,这表明ifn的诱导可能与粘膜免疫系统和病毒抗ifn机制有关。这些结果为进一步研究鱼类中刺痛的作用和机理提供了基础。 (C)2016年不列颠群岛渔业协会

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号