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| 大鳍鳠免疫球蛋白轻链3型基因cDNA的克隆及表达 | |
| 引用本文： | 蒋自立,李春涛,张其中,陈 霞,李 超,杨莹莹.大鳍鳠免疫球蛋白轻链3型基因cDNA的克隆及表达[J].水产学报,2012,36(7):1011-1018. |
| 作者姓名： | 蒋自立 李春涛 张其中 陈 霞 李 超 杨莹莹 |
| 作者单位： | 1. 遵义师范学院,贵州遵义563000;西南大学生命科学学院,淡水生物生殖与发育教育部重点实验室,三峡库区生态环境教育部重点实验室,重庆400715 2. 西南大学生命科学学院,淡水生物生殖与发育教育部重点实验室,三峡库区生态环境教育部重点实验室,重庆400715 3. 暨南大学水生生物研究所,广东广州,510632 |
| 基金项目： | 国家“八六三”高技术研究发展计划(863计划，2011AA10A216) |
| 摘 要： | 应用同源克隆和RACE-PCR方法获得大鳍鳠免疫球蛋白轻链3型(IgL3)基因的全长cDNA序列,并分析了该基因在组织中的表达。大鳍鳠IgL3的cDNA全长为947 bp,包含5非编码区58 bp,3非编码区184 bp,开放阅读框705 bp,编码234个氨基酸。推测的蛋白质序列分为可变区(VL)和恒定区(CL)。VL被进一步划分为4个骨架区(FR)和3个互补决定区(CDR)。大鳍鳠与其它6种硬骨鱼类免疫球蛋白轻链L3氨基酸序列比对分析表明,大鳍鳠氨基酸序列与斑点叉尾IgL3型(F型)的相似性最高,为68.8%,与南极鱼IgL3型的相似性最低,为47.2%。进化树分析表明,大鳍鳠IgL与斑点叉尾IgL3型(F型)聚为一支并与其它硬骨鱼类IgL3型聚为一簇,明显与L1和L2进化支不同。实时荧光定量PCR显示,大鳍鳠IgL3基因主要在头肾、脾脏和血细胞中转录表达;注射嗜水气单胞菌后,头肾、脾脏和血细胞IgL3基因转录表达量有显著上升。研究表明,头肾、脾脏和血液是大鳍鳠IgL3型基因主要的表达器官,在免疫反应中起重要作用。 |
| 关 键 词： | 大鳍鳠 免疫球蛋白轻链3型基因 克隆 实时荧光定量PCR 表达 |
| 收稿时间： | 2011/12/13 0:00:00 |
| 修稿时间： | 3/7/2012 12:00:00 AM |
Molecular cloning and expression analysis of the immunoglobulin light chain (L3 isotype )gene cDNA in largefin longbarbel catfish(Mystus macropterus Bleeker) |
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| JIANG Zi-li,Li Chun-tao,ZHANG Qi-zhong,CHEN Xi,LI Chao and YANG Ying-ying.Molecular cloning and expression analysis of the immunoglobulin light chain (L3 isotype )gene cDNA in largefin longbarbel catfish(Mystus macropterus Bleeker)[J].Journal of Fisheries of China,2012,36(7):1011-1018. | |
| Authors: | JIANG Zi-li Li Chun-tao ZHANG Qi-zhong CHEN Xi LI Chao and YANG Ying-ying |
| Institution: | 1.Zunyi Normal College,Zunyi 563000,China;2.Key Laboratory of Freshwater Fish Reproduction and Development of Ministry of Education,Key Laboratory Eco-environments in Three Gorges Reservoir Region of Ministry of Education,School of Life Science,Southwest University,Chongqing 400715,China;3.Hydrobiology Institute of Jinan University,Guangzhou 510632,China) |
| Abstract: | The technique of homologous cloning and Rapid Amplification of cDNA Ends(RACE) was used to amplify full length cDNA of immunoglobulin light chain 3 isotype(IgL3) gene from largefin longbarbel catfish(Mystus macropterus Bleeker).IgL3 in M.macropterus has 947 nucleotides,including 5-UTR of 58 nucleotides,3-UTR of 184 nucleotides and an open reading frame with 705 nucleotides encoding a peptide of 234 amino acids.The deduced amino acid sequence contains an constant region(CL) and a variable domain(VL) consisting of 4 frame regions(FRs) and 3 complementary determining regions(CDRs).The IgL3 comparison in seven teleost species showed that IgL3 in M.macropterus shared the highest identity(68.8%) with that(F) in Ictalurus punctatus,and the lowest identity(47.2%) with that in Salmo salar.Phylogenetic tree based on some teleost IgL amino acids showed that IgL3 in M.macropterus was clustered closely with that(F) of I.punctatus and grouped with IgL3 in other teleost,and was far away from L1 and L2 of teleost.Real-time PCR showed that IgL3 mRNA expression of M.macropterus was mainly detected in head kidney,spleen and blood cells and increased significantly in these tissues after injection of Aeromonas hydrophila.The result indicated that head kidney,spleen and blood cell are main organs for IgL3 expression after stimulation,and play a critical role in immunity interaction in M.macropterus. |
| Keywords: | Mystus macropterus immunoglobulin L3 cloning real-time PCR expression |
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