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首页> 外文期刊>Fish & Shellfish Immunology >Molecular cloning and characterization of Mj-mov-10, a putative RNA helicase involved in RNAi of kuruma shrimp
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Molecular cloning and characterization of Mj-mov-10, a putative RNA helicase involved in RNAi of kuruma shrimp

机译:Mj-mov-10的分子克隆和特性分析,Mj-mov-10是一种参与黑头虾RNAi的推定RNA解旋酶

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摘要

Identification and characterization of the RNAi-related genes is the key to understanding RNAi mechanism in shrimp. In this study, we have identified and characterized a novel putative RNA helicase gene, Mj-mov-10 from the kuruma shrimp, Marsupenaeus japonicus and its implication in shrimp RNAi was demonstrated. The full-length Mj-mov-10 gene contained 3536 bp, including 239 bp of 5'UTR, 2895 bp of the open reading frame (ORF) and 402 bp of 3'UTR, respectively. An ORF of Mj-mov-10 could be translated to a 109-kDa protein which consists of a single helicase core domain containing seven signature motifs of the RNA helicase superfamily-1. Mj-MOV-10 protein shared 47% and 40% identity with mammalian MOV-10 and plant SDE3, respectively. Expression of Mj-mov-10 gene was significantly up-regulated upon dsRNA and white spot syndrome virus (WSSV) challenge. In vivo gene knockdown of Mj-mov-10 resulted in an increase of a susceptibility of shrimp to WSSV infection. Our results implied the functional significance of Mj-MOV-10 in dsRNA-mediated gene silencing and antiviral defense mechanism in shrimp. (C) 2015 Elsevier Ltd. All rights reserved.
机译:RNAi相关基因的鉴定和表征是了解虾RNAi机制的关键。在这项研究中,我们已经鉴定并鉴定了来自库鲁马虾,日本Marsupenaeus japonicus的新型推定RNA解旋酶基因Mj-mov-10及其在虾RNAi中的意义。全长Mj-mov-10基因包含3536 bp,其中包括5'UTR的239 bp,开放阅读框(ORF)的2895 bp和3'UTR的402 bp。 Mj-mov-10的ORF可以翻译成109-kDa蛋白,该蛋白由一个包含7个RNA解旋酶超家族1签名基元的解旋酶核心结构域组成。 Mj-MOV-10蛋白与哺乳动物MOV-10和植物SDE3分别具有47%和40%的同一性。 dsRNA和白斑综合症病毒(WSSV)攻击后,Mj-mov-10基因的表达明显上调。 Mj-mov-10的体内基因敲低导致虾对WSSV感染的敏感性增加。我们的结果暗示了Mj-MOV-10在对虾的dsRNA介导的基因沉默和抗病毒防御机制中的功能意义。 (C)2015 Elsevier Ltd.保留所有权利。

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