半滑舌鳎TLR5S 三种剪切型基因的克隆与表达分析
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作者单位:

1. 大连海洋大学 水产与生命学院, 辽宁 大连 116023; 2. 中国水产科学研究院 黄海水产研究所, 农业部海洋渔业资源重点实验室, 山东 青岛 266071; 3. 青岛海洋科学与技术国家实验室, 海洋渔业科学与食物产出过程功能实验室, 山东 青岛 266071; 4. 上海海洋大学 水产与生命学院

作者简介:

作者简介: 张文婷(1988−), 女, 硕士研究生, 研究方向为鱼类生物技术. E-mail: wen0zi1988@126.com 通信作者: 陈松林, 研究员, 博导, 从事鱼类生物技术研究. Tel: 0532-85844606; E-mail: chensl@ysfri.ac.cn

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中图分类号:

S917

基金项目:

国家自然科学基金重点项目(31530078); 山东省泰山学者攀登计划专项.


Molecular cloning, characterization, and expression of three TLR5S splicing variants in half-smooth tongue sole
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Affiliation:

1. College of Fisheries and Life Science, Dalian Ocean University, Dalian, Liaoning 116023, China; 2. Key Laboratory for Sustainable Development of Marine Fisheries, Ministry of Agriculture, Yellow Sea Fisheries Research Institute, Chinese Academy of Fish

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    摘要:

    Toll 样受体5 (Toll-like receptor 5, TLR5)是TLRs 家族成员之一, 可分为跨膜型TLR5M 和鱼类特有的可溶型TLR5S, 它们可以识别致病菌表面的鞭毛蛋白并协同作用激活免疫反应。为了研究半滑舌鳎受到病原感染后TLR5S参与免疫反应的作用, 本研究使用RACE 技术获得了半滑舌鳎(Cynoglossus semilaevis)TLR5S 全长cDNA 序列。TLR5ScDNA有3 种剪切型: Cs.TLR5S x1, Cs.TLR5S x2 和Cs.TLR5S x3。这3 种剪切型的相同区域为308 bp 5′非编码区(5′UTR)和1701 bp 开放阅读框(ORF), 不同的3′UTR 分别为138 bp、364 bp 和637 bp。Cs.TLR5S 共编码567 个氨基酸, 预测编码蛋白质分子量为64.03 kD, 等电点为8.49。氨基酸多重序列比对结果显示, Cs.TLR5S 氨基酸序列与其他脊椎动物TLR5S 氨基酸序列具有较高的相似性, 其中与牙鲆相似度高达61%, 表明Cs.TLR5S 在进化上的具有一定的保守性。Real-time PCR 结果表明该基因在半滑舌鳎的不同组织均有表达, 其中在肝的表达量最高, 在脾的表达量最低。此外, 检测Cs.TLR5S 3′端的不同剪切型在肝、脾、头肾、小肠中的表达, 结果显示Cs.TLR5S x3 只在肝中高表达, 而Cs.TLR5S x1 则在肝和小肠中都有中等程度表达。鳗弧菌(Vibrio anguillarum)感染半滑舌鳎实验表明, 注射菌液6 h 后,Cs.TLR5S 基因在肾、小肠、肝和脾4 个组织中的表达量都有显著上升; 注射鳗弧菌48 h 后, 以上4 种组织中表达量均呈现降低的变化。上述实验结果说明, Cs.TLR5S 基因可能参与了半滑舌鳎抗弧菌感染的免疫反应。

    Abstract:

    Toll-like receptor (TLR) 5 plays a vital role in bacterial flagellin recognition and immune responsealerts in vertebrates. In the present study, the synergistic role of the TLR5 membrane form and the TLR5 solubleform (TLR5S) are reported in a bony fish. The full-length TLR5S cDNA was cloned using homologous cloningand rapid amplification of cDNA ends techniques to study the regulatory role of TLR5S in the innate immune responseof half-smooth tongue sole, Cynoglossus semilaevis, (designated Cs.TLR5S). Three alternative splicingvariants (Cs.TLR5S x1, Cs.TLR5S x2, and Cs.TLR5S x3) of the Cs.TLR5S cDNA sequence were found in C. semilaevis.The full-length CsTLR5S cDNA included a 308 bp 5′-untranslated region (UTR), a 1701 bp open readingframe, and 138 bp, 364 bp, and 637 bp 3′-UTRs, respectively. The cDNA encoded a polypeptide of 567 aminoacids, with a molecular mass of 64.03 kD and an isoelectric point of 8.49. Multiple sequence alignment revealedthat the Cs.TLR5S proteins are well conserved with a typical modular architecture and identical active sitesthroughout vertebrates, and shared the highest identity with Paralichthys olivaceus TLR5S (61%), suggesting aconserved function for TLR5S. A phylogenetic analysis indicated that Cs.TLR5S and homologous TLR5S sequencesfrom teleosts were clustered into a clade, and Cs.TLR5S was separated from another clade with amphibians,mammals, and other vertebrates. A tissue expression profile analysis using the quantitative real-time polymerasechain reaction (qRT-PCR) showed that Cs.TLR5S mRNA was constitutively expressed in all tested tissues,with predominant expression in liver and the lowest expression in spleen. Alternative splicing of the 3′-UTR usingqRT-PCR showed that Cs.TLR5S x3 was only expressed in liver, whereas Cs.TLR5S x1 was expressed in liver andintestine. In addition, Cs.TLR5S was expressed at different levels in liver, spleen, intestine, and head kidney after aVibrio anguillarum challenge. These results suggest that expression of the C. semilaevis Cs.TLR5S variants aredifferentially regulated in different tissues and play important roles in the immune response against bacterialpathogens.

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张文婷,向晋松,李海龙,张宁,董忠典,高峰涛,陈松林.半滑舌鳎TLR5S 三种剪切型基因的克隆与表达分析[J].中国水产科学,2016,23(1):10-20
ZHANG Wenting, XIANG Jinsong, LI Hailong, ZHANG Ning, DONG Zhongdian, GAO Fengtao, CHEN Songlin. Molecular cloning, characterization, and expression of three TLR5S splicing variants in half-smooth tongue sole[J]. Journal of Fishery Sciences of China,2016,23(1):10-20

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  • 在线发布日期: 2016-01-12
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