Molecular cloning and expression analysis of chickenMyD88andTRIFgenes

特里夫 基因 生物 打开阅读框 互补DNA 克隆(编程) 序列分析 先天免疫系统 遗传学 编码区 肽序列 Toll样受体 分子生物学 受体 计算机科学 程序设计语言
作者
Sarah Wheaton,Sarah Wheaton,Melissa D. Lambourne,Sarah Wheaton,Melissa D. Lambourne,Aimie J. Sarson,Jennifer T. Brisbin,Ashraf Mayameei,Shayan Sharif
出处
期刊:Dna Sequence 卷期号:18 (6): 480-486 被引量:36
标识
DOI:10.1080/10425170701295856
摘要

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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