Northeast Chinese lamprey (Lethenteron morii) MyD88: Identification, expression, and functional characterization

被引:5
作者
Zhou, Zebin [1 ,2 ,3 ]
Ding, Shaoqing [1 ,2 ,3 ]
He, Yuanyuan [1 ,2 ,3 ]
Ren, Jianfeng [1 ,2 ,3 ]
Li, Weiming [4 ]
Zhang, Qinghua [1 ,2 ,3 ]
机构
[1] Shanghai Ocean Univ, Key Lab Explorat & Utilizat Aquat Genet Resources, Minist Educ, Shanghai 201306, Peoples R China
[2] Shanghai Ocean Univ, Int Res Ctr Marine Biosci, Minist Sci & Technol, Shanghai 201306, Peoples R China
[3] Shanghai Ocean Univ, Key Lab Freshwater Aquat Genet Resources, Minist Agr, Shanghai 201306, Peoples R China
[4] Michigan State Univ, Dept Fisheries & Wildlife, E Lansing, MI 48824 USA
基金
中国国家自然科学基金;
关键词
Lamprey; Myeloid differentiation factor 88; Molecular cloning; Expression analysis; Subcellular localization; ADAPTER PROTEIN; INNATE IMMUNITY; GENE; TIR; RECOGNITION; PATTERN; INTERLEUKIN-1; LOCALIZATION; ZEBRAFISH; BINDING;
D O I
10.1016/j.fsi.2019.09.035
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Myeloid differentiation factor 88 (MyD88) is a key adaptor of Toll-like receptors (TLR), an important pattern recognition receptor of the innate immune system. To study the origin and evolution of the vertebrate TLR signaling pathway in innate immune systems, we analyzed the biological characteristics and functions of the MyD88 gene in Northeast Chinese lamprey (Lethenteron morii) using PCR amplification, real-time PCR analysis, dual luciferase reporter gene assay, immunofluorescence assay, and other methods. Bioinformatics analysis showed that LmMyD88 has a modular structure consisting of Toll/IL-1R domain (TIR) and death domain (DD), which is typical of the MyD88 family. A phylogenetic tree showed that the homology of LmMyD88 was consistent with the phylogenetic status of lampreys. Tissue expression analysis indicated that the mRNA expression was exprecsPd in some normal tissues of larval and adult L. morii. Real-time PCR analysis showed that the expression of LmMyD88 in tissues, such as gill and kidney, of the adult increased significantly after infection by Pseudomonas aeruginosa. Subcellular localization results showed that LmMyD88 was expressed in the nucleus, cytoplasm, and other parts. A dual luciferase reporter assay indicated that LmMyD88 activated nuclear factor kappa B downstream of the TLR signaling pathway. This study suggested that LmMyD88 might play an important role in the innate immune signal transduction process of L. morii.
引用
收藏
页码:539 / 547
页数:9
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