Molecular cloning, characterization, and expression of three TLR5S splicing variants in half-smooth tongue sole
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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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S917

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    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]. Jounal of Fishery Sciences of China, 2016,[volume_no](1):10-20

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  • Online: January 12,2016
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