Wang Mengqiang, Wang Lingling, Yi Qilin, Gai Yunchao, Song Linsheng
Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, 7 Nanhai Rd., Qingdao 266071, China.
Key Laboratory of Mariculture & Stock Enhancement in North China's Sea, Ministry of Agriculture, Dalian Ocean University, Dalian 116023, China.
Fish Shellfish Immunol. 2015 Nov;47(1):407-17. doi: 10.1016/j.fsi.2015.09.035. Epub 2015 Sep 21.
Superoxide dismutase (SOD) functions as the first and essential enzyme in the antioxidant system and is ubiquitously existed in both prokaryotes and eukaryotes. In the present study, both cytoplasmic and mitochondrial manganese SOD were identified from Chinese mitten crab Eriocheir sinensis (designed as EscytMnSOD and EsmtMnSOD). The complete nucleotide sequence of EscytMnSOD comprised 1349 bp and consisted of a 5' untranslated regions (UTR) of 43 bp, a 3' UTR of 445 bp and an open reading frame (ORF) of 861 bp encoding a polypeptide of 286 amino acid residues. The full-length cDNA sequence of EsmtMnSOD comprised 990 bp, containing a 5' UTR of 55 bp, a 3' UTR of 278 bp and an ORF of 657 bp encoding a polypeptide of 218 amino acid residues. The deduced amino acid sequences of EscytMnSOD and EsmtMnSOD contained highly conserved MnSOD signature and typical functional domain, and exhibited high similarity with their reported homologues. In the phylogenetic tree, EscytMnSOD and EsmtMnSOD were clustered with their homologues from the land crab Cardisoma armatum. The EscytMnSOD and EsmtMnSOD transcripts were constitutively expressed in haemocytes, muscle, heart, gill, haepatopancreas and gonad, with the highest expression level in gills and haepatopancreas, respectively. The mRNA expression levels of them were all up-regulated in haemocytes with similar profiles after the stimulation of Vibrio anguillarum, Micrococcus luteus and Pichia pastoris. The EsmtMnSOD with low basal expression level responded to invading microbes intensely, while the EscytMnSOD with high basal expression level exhibited mild responses against stimulating microbes. The purified rEscytMnSOD and rEsmtMnSOD proteins exhibited specific Mn(2+)-dependent enzymatic activities, while rEscytMnSOD with lower basic activity displayed higher stability than rEsmtMnSOD. All these results indicated that EscytMnSOD and EsmtMnSOD were efficiently antioxidant enzymes and potentially involved in the innate immune responses of E. sinensis with different roles, the former might play a routine role in the innate immune system in crabs, while the later might be involved in the immune response against invading microbes specifically.
超氧化物歧化酶(SOD)作为抗氧化系统中的首个关键酶,在原核生物和真核生物中普遍存在。在本研究中,从中华绒螯蟹(Eriocheir sinensis)中鉴定出了细胞质和线粒体锰超氧化物歧化酶(分别命名为EscytMnSOD和EsmtMnSOD)。EscytMnSOD的完整核苷酸序列为1349 bp,由43 bp的5'非翻译区(UTR)、445 bp的3'UTR和861 bp的开放阅读框(ORF)组成,该ORF编码一个由286个氨基酸残基组成的多肽。EsmtMnSOD的全长cDNA序列为990 bp,包含55 bp的5'UTR、278 bp的3'UTR和657 bp的ORF,编码一个由218个氨基酸残基组成的多肽。EscytMnSOD和EsmtMnSOD推导的氨基酸序列含有高度保守的锰超氧化物歧化酶特征和典型的功能结构域,并且与其已报道的同源物具有高度相似性。在系统发育树中,EscytMnSOD和EsmtMnSOD与其来自武装圆轴蟹(Cardisoma armatum)的同源物聚类在一起。EscytMnSOD和EsmtMnSOD转录本在血细胞、肌肉、心脏、鳃、肝胰腺和性腺中组成性表达,在鳃和肝胰腺中的表达水平最高,分别为最高。在鳗弧菌(Vibrio anguillarum)、藤黄微球菌(Micrococcus luteus)和毕赤酵母(Pichia pastoris)刺激后,它们在血细胞中的mRNA表达水平均上调,且具有相似的表达模式。基础表达水平较低的EsmtMnSOD对入侵微生物反应强烈,而基础表达水平较高的EscytMnSOD对刺激微生物的反应较温和。纯化的重组EscytMnSOD和重组EsmtMnSOD蛋白表现出特定的依赖锰离子的酶活性,而基础活性较低的重组EscytMnSOD比重组EsmtMnSOD具有更高的稳定性。所有这些结果表明,EscytMnSOD和EsmtMnSOD是有效的抗氧化酶,并可能以不同的作用参与中华绒螯蟹的先天免疫反应,前者可能在蟹的先天免疫系统中发挥常规作用,而后者可能特别参与针对入侵微生物的免疫反应。