鸡MyD88和TRIF基因的克隆及表达分析。

Sarah Wheaton, Melissa D Lambourne, Aimie J Sarson, Jennifer T Brisbin, Ashraf Mayameei, Shayan Sharif
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引用次数: 37

摘要

toll样受体(TLRs)通过对微生物的特定成分作出反应来触发先天免疫系统。MyD88和TRIF是包含Toll/白细胞介素(IL)-1 (TIR)结构域的适配器,它们分别通过MyD88依赖性和非依赖性途径在tlr介导的信号传导中发挥重要作用。编码若干tlr的基因已经在鸡的基因组中被鉴定出来,然而,它们的信号通路的要素尚未被很好地表征。本文描述了鸡MyD88和TRIF同源基因的克隆,并分析了这些基因的时空表达。结果显示,鸡MyD88 cDNA具有1104 bp的开放阅读框(ORF),编码的预测蛋白序列为368 aa,由于一个过早终止密码子,比先前公布的编码序列短8 aa。MyD88基因在除肌肉外的所有组织中均有表达。鸡TRIF cDNA的ORF长度为2205 bp,编码735 aa的预测蛋白序列,与人TRIF蛋白序列的相似性为37.3%,同源性为28.9%。TRIF在所有组织中普遍表达。
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Molecular cloning and expression analysis of chicken MyD88 and TRIF genes.

Toll-like receptors (TLRs) trigger the innate immune system by responding to specific components of microorganisms. MyD88 and TRIF are Toll/interleukin (IL)-1 (TIR)-domain containing adapters, which play essential roles in TLR-mediated signalling via the MyD88-dependant and -independent pathways, respectively. Genes encoding several TLRs have been identified in the chicken genome, however, elements of their signalling pathways have not been well characterized. Here we describe the cloning of chicken MyD88 and TRIF orthologs, and examine the spatial and temporal expression of these genes. The chicken MyD88 cDNA was shown to have an open reading frame (ORF) of 1104 bp, encoding a predicted protein sequence of 368 aa, 8 aa short of a previously published coding sequence due to a premature stop codon. MyD88 gene expression was detected in each tissue tested except in muscle. The chicken TRIF cDNA possessed an ORF of 2205 bp, encoding a predicted protein sequence of 735 aa, which shared 37.3% similarity and 28.9% identity to human TRIF protein sequence. TRIF was ubiquitously expressed in all tissues.

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