Qian Gao, Yan-Wei Li, Wen-Ling Huang, Qin-Ping Zhao, Hui-Fen Dong
Department of Parasitology, School of Basic Medical Sciences, Wuhan University, Hubei Province, Wuhan 430071, China.
Zhongguo Xue Xi Chong Bing Fang Zhi Za Zhi. 2017 Mar 1;29(2):174-181. doi: 10.16250/j.32.1374.2016267.
To identify a myeloid differentiation factor 88 (MyD88) in , and characterize the role of MyD88 against infection.
The complete cDNA of MyD88 in was obtained by using rapid amplification of cDNA ends (RACE), and homologues sequences and conserved domains were aligned and the structure of MyD88 was predicted either. A phylogenetic tree of MyD88 was further constructed with other species. In addition, the mRNA expression level of MyD88 before and after infection was investigated by real-time quantitative PCR (RT-qPCR).
The cDNA of MyD88 consisted of 1 406 bp open reading frame (ORF), encoding 468 amino acid residues, which contained death domain and Toll/interlrukin-1 receptor (TIR) domain, the typical features of MyD88 family proteins. The predicted amino acid sequence of MyD88 shared 38%-52% identity with other mollusc. MyD88 was phylogenetically closeted to Biomphalaria glabrata MyD88. The MyD88 existed in all selected tissues and expressed highly in hemocyte, up-regulated after infection in all selected tissues except cephalopodium, especially higher in whole snail and hemocyte.
MyD88-dependent signaling pathway is present in and plays an important role in innate immune response against infection.
鉴定[某种生物名称未给出]中的髓样分化因子88(MyD88),并表征MyD88在抵抗[感染源未给出]感染中的作用。
采用cDNA末端快速扩增(RACE)法获得[该生物名称未给出]中MyD88的完整cDNA,比对同源序列和保守结构域并预测MyD88的结构。进一步构建MyD88与其他物种的系统发育树。此外,通过实时定量PCR(RT-qPCR)研究[该生物名称未给出]感染前后MyD88的mRNA表达水平。
[该生物名称未给出]MyD88的cDNA由1406bp的开放阅读框(ORF)组成,编码468个氨基酸残基,包含死亡结构域和Toll/白细胞介素-1受体(TIR)结构域,这是MyD88家族蛋白的典型特征。预测的[该生物名称未给出]MyD88氨基酸序列与其他软体动物的同源性为38%-52%。[该生物名称未给出]MyD88在系统发育上与光滑双脐螺MyD88最为接近。[该生物名称未给出]MyD88存在于所有选定组织中,在血细胞中高表达,在[感染源未给出]感染后,除头足部外的所有选定组织中均上调,在整个蜗牛和血细胞中尤其更高。
MyD88依赖的信号通路存在于[该生物名称未给出]中,在抵抗[感染源未给出]感染的先天免疫反应中起重要作用。