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首页> 外文期刊>Fish & Shellfish Immunology >Molecular cloning and immune responsive expression of MDA5 gene, a pivotal member of the RLR gene family from grass carp Ctenopharyngodon idella.
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Molecular cloning and immune responsive expression of MDA5 gene, a pivotal member of the RLR gene family from grass carp Ctenopharyngodon idella.

机译:MDA5 基因的分子克隆和免疫应答表达,该基因来自草鱼 Ctenopharyngodon idella 的RLR基因家族的关键成员。

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The cytoplasmic helicase protein MDA5 (melanoma-differentiation-associated gene-5) recognizes long molecules of viral double-stranded RNA (dsRNA) and single-stranded RNA with 5' triphosphate and mediates type I interferon secretion. In the present study, the first MDA5 gene in fish was cloned and characterized from grass carp Ctenopharyngodon idella. The full length of the C. idella MDA5 (CiMDA5) cDNA is 3233 nucleotides in length and encodes a polypeptide of 961 amino acids. The deduced amino acid sequence contained six main structural domains: a CARD (caspase activation and recruitment domain), a DEXDc (DEAD/DEAH box helicase domain), a ResIII (conserved restriction domain of bacterial type III restriction enzyme), two HELICc (helicase superfamily c-terminal domain) and an RD (regulatory domain). The CiMDA5 mRNA was widespread expression in the tested tissues, was high level in spleen, skin and gill tissues, and was up-regulated by GCRV injection by semi-quantitative RT-PCR assay. The CiMDA5 transcripts in spleen were significantly up-regulated at 12 h (1.80 folds, P<0.05), reached the crest at 24 h (7.48 folds, P<0.05), and then recovered to normal level at 48 h post-injection (P
机译:胞质解旋酶蛋白 MDA5 (黑色素瘤分化相关基因5)识别具有5'三磷酸的病毒双链RNA(dsRNA)和单链RNA的长分子,并介导I型干扰素的分泌。在本研究中,从草鱼中华绒螯蟹(Ctenopharyngodon idella )中克隆并鉴定了鱼类中的第一个 MDA5 基因。 C的全长。 idella MDA5 ( CiMDA5 )cDNA的长度为3233个核苷酸,编码961个氨基酸的多肽。推导的氨基酸序列包含六个主要结构域:一个CARD(胱天蛋白酶激活和募集域),一个DEXDc(DEAD / DEAH盒解旋酶域),一个ResIII(细菌III型限制性酶的保守限制性域),两个HELICc(解旋酶)超家族c末端域)和RD(调节域)。 CiMDA5 mRNA在受试组织中广泛表达,在脾,皮肤和g组织中高水平表达,并且通过半定量RT-PCR分析法通过GCRV注射上调。脾脏的 CiMDA5 转录本在12 h时显着上调(1.80倍, P <0.05),在24 h时达到峰值(7.48倍, P) <0.05),然后在注射草鱼呼肠孤病毒(GCRV)后48小时( P mRNA的时间表达在48小时时显着增加(5.00倍, P <0.05),并在72小时时恢复到对照水平( P 参与了草鱼GCRV抗病毒先天免疫防御的早期阶段,为RLR(RIG-I样受体)基因家族的进化研究提供了新的见识。

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