军曹鱼Ig κ轻链cDNA克隆及组织表达分析
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1. 中国水产科学研究院 南海水产研究所, 广东 广州 510300;2. 华南农业大学, 广东 广州510642

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侯月娥(1983), 女, 硕士研究生, 主要从事分子生物学方面的研究.

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中央级公益性科研院所基本科研业务费专项资金项目(2007ZD10).


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    摘要:

    技术克隆了军曹鱼Ig κ, 969 bp端188 bpUTR开放阅读框为分子量约为Ig Seriola quinqueradiata 恒定区氨基酸序列 Ictalurus punctatus等鱼的轻链均为同大西洋鲑的发现在健康鱼体中)尤其在头肾、肠、鳃和脾中的表达量较正常水平明显升高κ是免疫球蛋白的主要表达场所

    Abstract:

    The technique of homologous cloning and Rapid Amplification of cDNA Ends(RACE) was used to amplify full length cDNA gene of immunoglobulin light chain(κ chain) from cobia ( Linnaeus). The full length cDNA of κ in cobia is 969 bp, containing a 3′ untranslated region (UTR) of 188 bp, a 5′ UTR of 52 bp, and an open reading frame (ORF) of 729 bp, encoding 242 amine acids. The estimated molecular weight of Ig κ is 26.255 kD, and the theoretical isoelectric point is 7.52. The deduced Igκ amino acid sequences of cobia were compared with those of other teleost species. For the constant region of Igκ, higher percentage similarity was obtained from comparisons between and between andhigher percentage similarity was obtained from comparisons between R. canadium By the phylogenetic tree of immunoglobulin light chain constant region, Igκ amino acid sequences of cobia were clustered with IgL thwere clustered together. The expression of Igκ gene in healthy cobia was initially measured by existed more obviously in liver and gill than in other tissues, but they were hardly expressed in intestine and gill increased obviously after cobia was immunized by intraperitoneal injection withThe and gill are main organs for Igκ production after and play a critical role in host-pathogen interaction

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侯月娥,冯娟,宁章勇,茅莉娜,郭志勋,许海东,孔小明.军曹鱼Ig κ轻链cDNA克隆及组织表达分析[J].中国水产科学,2011,18(1):48-58
.[J]. Journal of Fishery Sciences of China,2011,18(1):48-58

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  • 在线发布日期: 2011-01-13
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