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虎虾(Penaeus monodon)核因子红细胞 2 相关因子 2(Nrf2)的鉴定与功能研究。

Characterization and functional study of nuclear factor erythroid 2-related factor 2 (Nrf2) in black tiger shrimp (Penaeus monodon).

机构信息

Key Laboratory of Aquatic Product Processing, Ministry of Agriculture and Rural Affairs, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou, 510300, PR China; Guangdong Provincial Key Laboratory of Fishery Ecology and Environment, Guangzhou, 510300, PR China.

Key Laboratory of Aquatic Product Processing, Ministry of Agriculture and Rural Affairs, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou, 510300, PR China.

出版信息

Fish Shellfish Immunol. 2021 Dec;119:289-299. doi: 10.1016/j.fsi.2021.10.016. Epub 2021 Oct 14.

Abstract

Nuclear factor erythroid 2-related factor 2 (Nrf2) is a member of the Cap'n'collar basic region leucine zipper (CNC-bZIP) transcription factor family, and is activated by diverse oxidants, pro-oxidants, antioxidants and chemopreventive agents. The full-length cDNA of Nrf2 from Penaeus monodon (PmNrf2; 2024 bp long with 729 bp coding region, GenBank accession no. MW390830) was cloned. The 242-amino-acid polypeptide encoded by this gene had a predicted molecular mass of 27.80 kDa. Sequence homology and phylogenetic analysis showed that PmNrf2 was similar to the insect Cap'n'Collar (CNC) transcription factor and mammalian Nrf2. Tissue expression profile analyzed by quantitative real-time RT-PCR (qRT-PCR) demonstrated that PmNrf2 was constitutively expressed in all examined tissues, with the highest expression observed in the intestines and the weakest expression observed in the hemocyte. PmNrf2 expression profiles were detected in the hepatopancreas of shrimp after bacterial challenge. The results suggested that PmNrf2 was involved in the responses to bacterial challenge, but the temporal expression pattern trend of PmNrf2 differed between the gram-negative and gram-positive bacterial challenges in the shrimp hepatopancreas. The recombinant PmNrf2 protein was expressed and purified through affinity chromatography. Furthermore, an anti-PmNrf2 polyclonal antibody was obtained, which was able to clearly detect PmNrf2 protein expression in the hepatopancreas of shrimp. Knockdown of PmNrf2 by RNA interference (RNAi) resulted in a reduction in the expression of PmGPx gene. Taken together, the results of our study indicated that PmNrf2 played a role in regulation the transcription of PmGPx antioxidant enzyme genes.

摘要

核因子红细胞 2 相关因子 2(Nrf2)是 Cap'n'collar 碱性区域亮氨酸拉链(CNC-bZIP)转录因子家族的成员,可被多种氧化剂、前氧化剂、抗氧化剂和化学预防剂激活。斑节对虾(Penaeus monodon)Nrf2 的全长 cDNA(PmNrf2;长 2024bp,编码区 729bp,GenBank 登录号 MW390830)被克隆。该基因编码的 242 个氨基酸的多肽预测分子量为 27.80 kDa。序列同源性和系统发育分析表明,PmNrf2 与昆虫 Cap'n'Collar(CNC)转录因子和哺乳动物 Nrf2 相似。通过定量实时 RT-PCR(qRT-PCR)分析组织表达谱表明,PmNrf2 在所有检测组织中均持续表达,在肠中表达最高,在血细胞中表达最低。在虾肝胰腺中检测到细菌刺激后 PmNrf2 的表达谱。结果表明,PmNrf2 参与了对细菌刺激的反应,但 PmNrf2 在虾肝胰腺中革兰氏阴性和革兰氏阳性细菌刺激的时间表达模式趋势不同。通过亲和层析表达和纯化了重组 PmNrf2 蛋白。此外,获得了抗 PmNrf2 多克隆抗体,该抗体能够清楚地检测到虾肝胰腺中 PmNrf2 蛋白的表达。通过 RNA 干扰(RNAi)敲低 PmNrf2 导致 PmGPx 基因的表达减少。总之,我们的研究结果表明,PmNrf2 在调节 PmGPx 抗氧化酶基因的转录中发挥作用。

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