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中国明对虾 MAPKK 基因的分离与表达分析及其对白斑综合征病毒感染的响应。

Isolation and expression analysis of an MAPKK gene from Fenneropenaeus chinensis in response to white spot syndrome virus infection.

机构信息

Key Laboratory for Sustainable Utilization of Marine Fisheries Resources, Ministry of Agriculture, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, 106 Nanjing Road, Qingdao, 266071, PR China.

Key Laboratory for Sustainable Utilization of Marine Fisheries Resources, Ministry of Agriculture, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, 106 Nanjing Road, Qingdao, 266071, PR China; Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, 1 Wenhai Road, Qingdao, 266300, PR China.

出版信息

Fish Shellfish Immunol. 2016 Aug;55:116-22. doi: 10.1016/j.fsi.2016.05.004. Epub 2016 May 6.

Abstract

Mitogen-activated kinase kinase (MAPKK) is an important gene involved in the host-virus interaction process. To obtain a better understanding of MAPKK in the interaction process between the Chinese shrimp Fenneropenaeus chinensis and white spot syndrome virus (WSSV), we cloned the sequence of an MAPKK cDNA from F. chinensis (FcMAPKK) and investigated the effect of FcMAPKK on WSSV infection. The results showed that the FcMAPKK gene contained a 1227 bp open reading frame (ORF), which encoded a highly conserved protein with a serine/threonine protein kinase catalytic (S_TKc) domain. The deduced amino acid sequence of FcMAPKK shared identities between 11.9 and 92.6% with MAPKKs from vertebrate, invertebrate, plant and fungus species. The FcMAPKK was expressed in all the examined tissues in the normal F. chinensis. FcMAPKK expression level was highest in the hepatopancreas where it was approximately 2.6-fold the expression level in the gill, and lowest in the muscle where it was approximately 0.3-fold the expression level in the hepatopancreas. The FcMAPKK expression levels in the muscle, gill, and hepatopancreas were all changed post WSSV challenge. The FcMAPKK expression was significantly (P < 0.01) up-regulated in the muscle of F. chinensis at 48 h post WSSV infection. The WSSV began to replicate quickly in the normal F. chinensis at 48 h post infection, while the WSSV replication in the U0126-treated F. chinensis could be significantly (P < 0.05) inhibited. The results suggested that FcMAPKK might be involved in the WSSV infection process, and hijacking of FcMAPKK might be required for WSSV replication in F. chinensis.

摘要

丝裂原活化蛋白激酶激酶(MAPKK)是参与宿主-病毒相互作用过程的重要基因。为了更好地了解中国对虾(Fenneropenaeus chinensis)与白斑综合征病毒(WSSV)相互作用过程中的 MAPKK,我们从中国对虾克隆了 MAPKK cDNA 序列(FcMAPKK),并研究了 FcMAPKK 对 WSSV 感染的影响。结果表明,FcMAPKK 基因含有 1227bp 的开放阅读框(ORF),编码一种高度保守的蛋白,具有丝氨酸/苏氨酸蛋白激酶催化(S_TKc)结构域。FcMAPKK 的推导氨基酸序列与脊椎动物、无脊椎动物、植物和真菌的 MAPKK 具有 11.9%至 92.6%的同一性。在正常的中国对虾中,FcMAPKK 在所有检测到的组织中均有表达。在肝胰腺中表达水平最高,约为鳃中的 2.6 倍,在肌肉中表达水平最低,约为肝胰腺中的 0.3 倍。肌肉、鳃和肝胰腺中的 FcMAPKK 表达水平在 WSSV 攻击后均发生变化。肌肉中的 FcMAPKK 表达在 WSSV 感染后 48 小时显著上调(P<0.01)。在正常的中国对虾中,WSSV 在感染后 48 小时开始快速复制,而 U0126 处理的中国对虾中的 WSSV 复制可显著(P<0.05)受到抑制。结果表明,FcMAPKK 可能参与了 WSSV 感染过程,而劫持 FcMAPKK 可能是 WSSV 在对虾中复制所必需的。

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