State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China.
Fish Shellfish Immunol. 2011 Apr-May;30(4-5):1159-69. doi: 10.1016/j.fsi.2011.03.002. Epub 2011 Mar 6.
The cytoplasmic helicase protein RIG-I (retinoic acid-inducible gene I) and downstream signaling molecules, MAVS (mitochondrial antiviral signaling protein), TRAF3 (TNF-receptor-associated factor 3) and TBK1 (TANK-binding kinase 1), have significant roles in the recognition of cytoplasmic 5'-triphosphate ssRNA and short dsRNA, and phosphorylation of IRF-3 (interferon regulatory factor 3) and IRF-7 which is responsible for the induction of type I interferons (IFN). In the present study, the full-length cDNAs of RIG-I, MAVS, TRAF3 and TBK1 were cloned and identified in common carp (Cyprinus carpio L.). The deduced protein of carp RIG-I is of 946 aa (amino acids), consisting of two CARDs (caspase-recruitment domain), a DEXDc (DExD/H box-containing domain), a HELICc (helicase superfamily c-terminal domain) and a RD (regulatory domain). Carp MAVS is of 585 aa, containing a CARD, a proline-rich region and a TM (transmembrane domain). Carp TRAF3 encodes a protein of 573 aa, including a RING (really interesting new gene), two TRAF-type zinc fingers, a coiled coil and a MATH-TRAF3 (meprin and TRAF homology) domain. Carp TBK1 is of 727 aa and contains a S_TKc domain (Serine/Threonine protein kinases, catalytic domain). Carp RIG-I, MAVS, TRAF3 and TBK1 mRNAs are ubiquitously expressed in all tissues examined. In response to SVCV infection, carp RIG-I and MAVS mRNAs were up-regulated at different levels in spleen, head kidney and intestine tissues at different time points. Similarly, both carp IRF-3 and IRF-7 mRNAs were significantly up-regulated in the detected tissues. Especially in intestine, the IRF-3 and IRF-7 mRNAs of carp increased and reached 25.3-fold (at 3 dpi) and 224.7-fold (at 5 dpi). Noteworthily, a significant growth of carp TRAF3 and TBK1 mRNA was also mainly found in intestine (7.0-fold and 11.3-fold at 5 dpi, respectively). These data implied that the expression profiles of IRF-3/-7 mRNAs in carp correlate with the up-regulation of RIG-I/MAVS/TRAF3/TBK, and carp RIG-I and MAVS may be involved in antiviral responses through the RIG-I viral recognition signaling pathway in a TRAF3/TBK1-dependent manner.
细胞质解旋酶蛋白 RIG-I(视黄酸诱导基因 I)及其下游信号分子,MAVS(线粒体抗病毒信号蛋白)、TRAF3(TNF 受体相关因子 3)和 TBK1(TANK 结合激酶 1),在识别细胞质 5'-三磷酸 ssRNA 和短 dsRNA 以及磷酸化 IRF-3(干扰素调节因子 3)和 IRF-7 方面具有重要作用,IRF-7 负责诱导 I 型干扰素(IFN)。在本研究中,鲤鱼(Cyprinus carpio L.)的全长 cDNA 克隆并鉴定了 RIG-I、MAVS、TRAF3 和 TBK1。鲤鱼 RIG-I 的推导蛋白由 946 个氨基酸组成,包含两个 CARD(半胱氨酸丰富区域)、一个 DEXDc(DExD/H 盒结构域)、一个 HELICc(解旋酶超家族 C 末端结构域)和一个 RD(调节结构域)。鲤鱼 MAVS 由 585 个氨基酸组成,包含一个 CARD、一个富含脯氨酸的区域和一个 TM(跨膜结构域)。鲤鱼 TRAF3 编码一个 573 个氨基酸的蛋白质,包括一个 RING(真正有趣的新基因)、两个 TRAF 型锌指、一个卷曲螺旋和一个 MATH-TRAF3(MEPRIN 和 TRAF 同源)结构域。鲤鱼 TBK1 由 727 个氨基酸组成,包含一个 S_TKc 结构域(丝氨酸/苏氨酸蛋白激酶,催化结构域)。鲤鱼 RIG-I、MAVS、TRAF3 和 TBK1 mRNA 在所有检测组织中均广泛表达。在 SVCV 感染后,鲤鱼 RIG-I 和 MAVS mRNA 在不同时间点在脾、头肾和肠组织中以不同水平上调。同样,鲤鱼 IRF-3 和 IRF-7 mRNA 在检测到的组织中也显著上调。特别是在肠道中,鲤鱼的 IRF-3 和 IRF-7 mRNA 增加,达到 25.3 倍(在 3 dpi)和 224.7 倍(在 5 dpi)。值得注意的是,在肠道中,鲤鱼 TRAF3 和 TBK1 mRNA 的显著生长也主要发现(在 5 dpi 时分别为 7.0 倍和 11.3 倍)。这些数据表明,IRF-3/-7 mRNAs 在鲤鱼中的表达谱与 RIG-I/MAVS/TRAF3/TBK 的上调相关,鲤鱼 RIG-I 和 MAVS 可能通过 TRAF3/TBK1 依赖性 RIG-I 病毒识别信号通路参与抗病毒反应。